Total 23 Senior Executive level Science / R&D / Research job vacancies in Coventry Southfields Old School, South Street, Coventry, CV1 5EJ

What skills and experience we're looking for

Please see attached recruitment information pack.

What the school offers its staff

Please see attached recruitment information pack.

Commitment to safeguarding

Our organisation is committed to safeguarding and promoting the welfare of children, young people and vulnerable adults. We expect all staff, volunteers and trustees to share this commitment. Our recruitment process follows the keeping children safe in education guidance. Offers of employment may be subject to the following checks (where relevant): childcare disqualification Disclosure and Barring Service (DBS) medical online and social media prohibition from teaching right to work satisfactory references suitability to work with children You must tell us about any unspent conviction, cautions, reprimands or warnings under the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975.

Job Description:

• Stakeholder Engagement and Needs Assessment: Collaborate with key stakeholders to identify their needs and clarify research/evaluation questions. Ensure alignment of priorities with the institution's, cluster’s, and ministry's vision, mission, and goals.
• Research and Evaluation Design: Contribute to the development of robust and rigorous research and evaluation methodologies for complex and specialized Health Services Research (HSR) studies.
• Data Collection and Analysis: Plan, oversee, and manage data collection efforts for health program evaluations and HSR studies. Analyze results, generate actionable insights, and communicate findings, highlighting strengths, areas for improvement, and recommendations to inform future health programs and services.
• Knowledge Dissemination: Promote interest in and disseminate valuable knowledge related to public health, health program evaluation, and outcomes research. Share findings with the broader healthcare community both nationally and internationally.
• Stakeholder Relationship Management: Expand and strengthen the stakeholder base for health program evaluations. Foster and maintain partnerships with existing collaborators to support ongoing research and evaluation efforts.

Requirements:

• Degree in Statistics, Mathematics, Public Health, or a related field.
  For Senior level: Minimum of a Master's or PhD in Public Health, Data Science, Statistics, or a related discipline.
• Proficiency in SPSS, STATA, or other statistical analysis software.
• Strong analytical skills, with the ability to interpret and summarize complex data accurately.
• Strong organizational skills and attention to detail.
  Ability to work independently and manage multiple tasks effectively.
  

Interested applicants, kindly furnish us with your detailed resume in MS Words format and click "Apply Now" button or email your resume to esther@jobstudio.com.sg

*We regret to inform only shortlisted candidates will be notified. Applicants who do not possess necessary experience or qualification will still be considered on individual merits and may be contacted for other opportunities. *

“JobStudio will not solicit any money, request to use your bank account for business or request you to transfer any monies to any parties, please be aware of scams impersonating JobStudio and our employees. You may call our office directly for verification. We will not be liable for loss arising from scams.”

JOBSTUDIO PTE LTD

EA License No: 10C4754

EA Personnel: Avena Esther

EA Personnel Reg No: R24120999

Part -time (0.4 FTE 14 hours per week), Fixed term position for 6 months based at Penrith campus (Kingswood)
Remuneration: $67,816 to $77,793 p.a. Including Super & Leave Loading
Benefit from flexible work arrangements, salary packaging, development opportunities and more

       Part -time (0.4 FTE 14 hours per week), Fixed term position for 6 months        Based at Penrith Campus (Kingswood)  About Western Sydney University Western Sydney University is a modern, forward-thinking, research-led university, located in the heart of Australias fastest-growing, economically significant region. The University has 11 campuses in Sydney, as well as campuses in Ho Chi Minh City, Vietnam, and Surabaya, Indonesia, with plans for two campuses in India. With over 200,000 alumni, almost 50,000 students, and approximately 3,500 staff, the University promotes a dynamic, inclusive, and innovative culture focused on research and dedicated to student-centered excellence. Our
... Click here to view more detail / apply for Ref 4891/24 Senior Research Fellow, School of Engineering, Design and Built Environment

What skills and experience we're looking for

We are seeking an experienced science professional who will provide a comprehensive efficient and effective range of technical support to meet the needs of the department. This will include preparation and maintenance of resources, ordering of supplies and supporting both staff and students in the classroom. You will need to be enthusiastic, flexible and confident in supporting practical work to A level. You may be required to work across all science departments, but specific departmental training will be provided where appropriate.

The post holder must at all times carry out their responsibilities within the spirit of the school and trust policies and within the framework of legislation relating to academies and education, with particular regard to the statutory responsibilities of the trust and the governing body of the school.

What the school offers its staff

Silverdale School is an extremely popular and high achieving 11-18 comprehensive in the south west of Sheffield and is the founding school of Chorus Education Trust. Silverdale has 1,450 students on roll including 450 in Silverdale Sixth Form. In 2020 it was named the Sunday Times Top State Secondary School in the North of the Decade, in recognition of its sustained success.

Silverdale has an excellent record of student achievement at both key stage 4 and key stage 5. At our heart is one of the country’s original teaching school hubs, the South Yorkshire Teaching Hub, which includes the Sheffield Teacher Training Alliance and National Modern Languages SCITT.

At Silverdale, we benefit from a new building with excellent facilities, which was expanded in 2023 to provide further state of the art teaching facilities and a dedicated Sixth Form centre.

Commitment to safeguarding

Our organisation is committed to safeguarding and promoting the welfare of children, young people and vulnerable adults. We expect all staff, volunteers and trustees to share this commitment. Our recruitment process follows the keeping children safe in education guidance. Offers of employment may be subject to the following checks (where relevant): childcare disqualification Disclosure and Barring Service (DBS) medical online and social media prohibition from teaching right to work satisfactory references suitability to work with children You must tell us about any unspent conviction, cautions, reprimands or warnings under the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975.

Job Description:

• Conduct statistical analysis and provide statistical support for research project
• Assisting identify stakeholders needs and clarifying the research/ evaluation question
• Planning and overseeing data collection to support related program evaluation
• Expanding the stakeholder base for health program evaluation and strengthening partnership with existing collaborators
• Performing data extraction and compiling statistical data for reporting

Requirement:

• Bachelor Degree with concentration in Statistics, Mathematics or equivalent

Interested applicants, kindly furnish us with your detailed resume in MS Words format and click Apply Now button.

**We regret to inform only shortlisted candidates will be notified. Applicants who do not possess necessary experience or qualification will still be considered on individual merits and may be contacted for other opportunities. **

** JobStudio will not solicit any money, request to use your bank account for business or request you to transfer any monies to any parties. Please be aware of scams impersonating JobStudio and our employees. You may call our office directly for verification. We will not be liable for any loss arising from scams. **

JOBSTUDIO PTE LTD

EA License No: 10C4754

EA Personnel No: R21101828

EA Personnel Name: Kam Xiu Ping

$114,307 - $160,728 (ALB - ALC) per annum, plus up to 17% superannuation
3 years full time fixed term appointment
Commencing immediately

Job Reference:  
 
John de Laeter Centre at Curtin University 
Est. in . The John de Laeter Centre is the core analytical facility at Curtin University, Western Australia, hosting more than $50M of advanced characterisation and analysis instrumentation operated by dedicated laboratory managers and technicians. We provide tailored geoscience services to the resources sectors to reduce risk, improve workflows and provide solutions. 
 
The John de Laeter Centre provides quantitative data used to understand processes of Earth and planetary evolution, characterise the nature of resources and materials upon which our society depends, and monitor our changing environment. 
 
For more information about the centre, please visit: https://jdlc.curtin.edu.au/research/  
 
Your new role: 
Curtin University is seeking a

... Click here to view more detail / apply for Research Fellow / Senior Research Fellow ? Geoscience Atom Probe (GAP) Facility

$139,625 - $160,728 (ALC), plus 17% superannuation.
Full time, two-year fixed term Teaching Academic appointment.
Be part of shaping the future of Actuarial Science through dynamic teaching.

Job Reference:
Your new role
Are you passionate about shaping the future of actuarial science through dynamic teaching and hands-on industry experience? Join our vibrant team at Curtin University as a Senior Lecturer in Actuarial Science and make a tangible impact on the next generation of actuaries.
This teachingfocused role would suit professionals with current industry experience, ready to inspire and mentor students in a specialised and rapidly evolving field.
Key Responsibilities:


Teaching Excellence: Deliver high-quality teaching in our Actuarial Science Program. As a Unit Coordinator, you'll play a pivotal role in shaping the curriculum and ensuring a robust learning experience.
Student Supervision: Oversee and guide student projects, including Honours and


... Click here to view more detail / apply for Senior Lecturer, Actuarial Science

Job Description:

• Provide administrative support to the department including procurement, maintain and track departmental assets/ equipment
• Provide scheduling and secretarial support to the department (Clinical Research Unit) such as managing calendars of department Director
• Coordinate department meeting and minutes writing
• Provide grant and project funding administrative support
• Assist in generating reports and data
• Any Ad Hoc duties as per assigned

Requirement:

• Diploma in Business Administration/ Project Management/ Health Service Management or equivalent

Interested applicants, kindly furnish us with your detailed resume in MS Words format and click "Apply Now" button.

** We regret to inform only shortlisted candidates will be notified. Applicants who do not possess necessary experience or qualification will still be considered on individual merits and may be contacted for other opportunities.**

** JobStudio will not solicit any money, request to use your bank account for business or request you to transfer any monies to any parties. Please be aware of scams impersonating JobStudio and our employees. You may call our office directly for verification. We will not be liable for any loss arising from scams. **

JOBSTUDIO PTE LTD

EA License No: 10C4754

EA Personnel: Kam Xiu Ping

EA Personnel Reg No: R21101828

We have an exciting opportunity to be part of a definitive trial examining the effectiveness of oral nutritional supplement use in care homes.

We seek to appoint a Post Doctoral Research Fellow to join a multi-disciplinary research team for the REFRESH (nutRition intervEntions For malnouRished oldEr adultS in care homes) trial. This is a large NIHR funded randomised controlled trial examining oral nutritional supplements in care homes over four years.

The trial is a multi-university collaboration led by Professor Mary Hickson and Professor Jane Murphy of Bournemouth University. It is supported by the PenCTU and includes collaborators from the University of Exeter (statistics, health economics and community geriatric expertise), University of Coventry (dietetic expertise), University of Southampton (geriatric expertise), as well as care home managers and public representatives.

Your main tasks will be to recruit, set-up and initiate sites (care homes), maintain excellent working relationships with the care homes, manage the three field workers (to help with site initiation), develop online training for care home staff, and manage the day-to-day running of the trial. You will be supported by a Research Assistant and line managed by Professor Hickson.

Applications are invited from highly motivated individuals with a PhD or equivalent within the field of nutrition and dietetics. You will have excellent communication and organisational skills, clinical research experience with older adults, and ideally will have worked in the care home sector. You will also have an ability to work both independently and as part of a team, be able to work to tight deadlines and be comfortable and resilient working under pressure. A knowledge of training other professionals and using online educational platforms will be an advantage.

The role will be based at the University of Plymouth, recruiting in Devon & Cornwall, Wessex and the Birmingham area with an opportunity to discuss a hybrid online and in person working pattern. You will be required to travel regularly to Plymouth and/or Bournemouth for meetings, as well as visiting care homes in all the regions listed above that may not be accessible by public transport.

Based in the Faculty of Health, the School of Health Professions has something for everyone interested in health and care-related professions and is committed to shaping students into the best health professionals they can be.

InterCity Place is the first-class new home for our healthcare teaching and research providing students with skills to meet the needs of 21st century careers. The School offers a unique interdisciplinary learning environment, where students from the largest breadth of healthcare disciplines in the South West can benefit from excellent skills and research laboratories, research-informed teaching, stimulating practice placements and teaching delivered by professionally registered academic staff.

The School is proud of the commitment to student voluntary work, staff–student partnership, strong professional values and our record of student achievement and student satisfaction. State-of-the-art facilities and equipment help students maximise their potential and develop their core skills, preparing them to embark on exciting and rewarding careers. The School holds an Athena SWAN Silver award demonstrating the University’s ongoing commitment to advancing gender equality and success for all.

Please demonstrate clearly in your supporting statement how you meet the essential and any desirable criteria outlined in the job description.

For an informal online discussion about the role please contact Mary Hickson (mary.hickson@plymouth.ac.uk) or Jane Murphy (jmurphy@bournemouth.ac.uk).

This role will require an Enhanced Disclosure and Barring Service Check plus a Adult's Barred List check.

The successful candidate may be required to obtain an ATAS Certificate prior to this research being undertaken.

Closing date: Midnight, Sunday 10th November 2024

Interviews will be on Thursday 21st November 2024, via a zoom meeting. You will be notified if you have been shortlisted or not.

This is a full-time position working 37 hours per week on a fixed-term basis until 31st December 2028 due to funding.

We offer a competitive salary package and a generous pension and holiday scheme. We also offer a range of other benefits/support mechanisms, including ongoing development opportunities, flexible working, staff networks and enhanced maternity, paternity and adoption leave.

A summary of our comprehensive benefits can be viewed here.

Remote working is available up to 3 days a week.

The Faculty of Health holds four Silver Athena Swan awards, which recognise our commitment to supporting gender equality within higher education.

Staff appointed within the Faculty of Health may be able to join the NHS pension scheme subject to eligibility criteria.

The University of Plymouth is an inclusive community where everyone is welcomed regardless of their background. To find out more about our inclusive community initiatives, such as Athena Swan and the Race Equality Charter, please visit our Equality, Diversity and Inclusion webpages.

We particularly welcome applicants from under-represented communities at the University of Plymouth, such as carers/parents, people with disabilities, ethnically diverse, LGBT+, and people from all socio-economic backgrounds.

We have an exciting opportunity in the School of Chemical, Materials and Biological Engineering, University of Sheffield for a highly motivated Research Technician, with experience in (bio)process development and/or biomanufacturing and laboratory management. On a project funded by CEPI, you will work as an integral member of the team building on our prior work and developing an end-to-end automated, continuous, compact, multi-product mRNA process-in-a-box: the RNAboxTM.

You will use your organisational, laboratory management, communication and technical skills to provide essential support to our team, led by Dr Zoltan Kis and Professor Mark Dickman, research activities and play a key role ensuring research projects are delivered to defined milestones.
You will preferably possess a good honours level degree or Higher National Diploma in a relevant scientific field, and have excellent communication and interpersonal skills along with key awareness in the functioning of the research laboratory environment. Experimental wet-lab skills, organisational skills, thorough documentation and teamwork skills are essential.

Benefits of the position include:
● 38 days annual leave (including closure days and Bank Holidays), with the possibility to purchase up to ten additional days.
● Up to 5 days of paid time off to cover emergency caring responsibilities.
● A commitment to work life balance including, flexible working opportunities and hybrid working where possible.
● A highly competitive pension scheme.
● Discounts at participating shops and cinemas, and a cycle to work scheme.
● A commitment to your development, with programmes, learning modules and mentoring schemes.
● An inclusive and diverse workplace.
● A commitment to your wellbeing, with confidential emotional support, support for those going through the menopause, experiencing fertility treatment and having a baby, paid leave for IVF treatment and more.
Further information can be found at https://www.sheffield.ac.uk/jobs/benefits

You will be based in the School of Chemical, Materials and Biological Engineering within the Kis Research Group. Our interdisciplinary school is leading scientific exploration and engineering expertise in sustainability solutions, biomedical innovation, and advanced materials. We address crucial issues such as climate change, energy poverty, affordable medicine, sustainable agriculture and green manufacturing. Our internationally renowned research is supported through funding from government and industrial sources in the UK and the rest of the globe. More information about our research can be found on our website: School of Chemical, Materials and Biological Engineering | CMBE | The University of Sheffield

We are committed to exploring flexible working opportunities which benefit the individual and University.

We build teams of people from different heritages and lifestyles from across the world, whose talent and contributions complement each other to greatest effect. We believe diversity in all its forms delivers greater impact through research, teaching and student experience.

The post holder will be responsible for the day to day management of several of the R&D clinical research studies and teams. The post holder will be supporting the safe conduct of research in accordance with the regulatory and legal frameworks relating to the planning, undertaking and closure of research studies providing assurance that the rights and well being of trial participants are protected.

Excellent support from the close-knit management team will be provided including a comprehensive induction package and the opportunity to really develop as a manager and leader of a patient focused, quality driven, cutting-edge service.

The post holder will be instrumental in implementing team objectives to enhance the performance and development of the research teams whilst providing guidance, education, leadership and co-ordinating the portfolio of research studies and clinical trials to deliver high quality research and clinical care.

The role integrates both clinical duties such as maintaining an active caseload and managerial duties; as such the post holder will be required to effectively manage their time to fulfil key responsibilities. It is also expected that the post holder will be flexible with hours of work as required to ensure that we are offering a service that best suits the needs of our patients.

The post holder will be employed by Research and Development department (R&D) to work within the central clinical research teams of Accident and Emergency, Critical care and Trauma and Orthopaedics, managing an allocated number of research teams.

However, it is expected that the post folder will work flexibly across other research speciality areas as service requirements dictate throughout the duration of their contract.

The post holder will be responsible for the day to day management of several of the R&D clinical research studies and teams. The post holder will be supporting the safe conduct of research in accordance with the regulatory and legal frameworks relating to the planning, undertaking and closure of research studies providing assurance that the rights and well being of trial participants are protected.

The job holder may be required to carry out other similar or related duties within their bounds of registration which do not fall within the work outlined which may reasonably be required to deliver a comprehensive research service to our patients. The Line Manager, in consultation with the post holder will undertake any review.

Closing Date: Please be advised that this job advert will close as soon as sufficient applications have been received. Please apply for this job as soon as you can, if interested.

University Hospitals Coventry and Warwickshire NHS Trust, rated as good by the Care Quality Commission, is one of the largest teaching Trusts in the UK.

We are extremely proud of our employees across our hospital sites, with high quality patient care at the heart of everything we do.

Boasting some of the most modern facilities in Western Europe, the Trust is renowned for being at the forefront of research and innovation as part of its blossoming reputation as a worldwide leader in healthcare.

We are proud to be recognised as a Pathway to Excellence®designated organisation – please click the link for further details about this prestigious award.Pathway To Excellence ® - University Hospitals Coventry & Warwickshire (uhcw.nhs.uk)

By joining our exciting journey, you will form part of a passionate, talented team and will be able to access a wide range of learning and development opportunities. There has never been a better time to join our team.

The Trust is committed to building an organisation that makes full use of the talents, skills, experience, and different perspectives available in our diverse society. We want everyone to feel they are respected, valued, can achieve their potential and receive the most appropriate and relevant care. We will create an environment where the equality and human rights principles of fairness, respect, equality, dignity and autonomy are promoted and are part of the organisation's core values.

Clinical

• Work autonomously to manage a caseload of patients acting as a professional to ensure care to patients is delivered according to Trust policies and procedures and the research protocol delivery high standards and continuity of clinical care for study participants.

• Maintain strong relationships and communication channels with other key personnel such as multidisciplinary teams, clinical wards areas.

• Attend Multi-disciplinary Meetings, and appropriate clinics, to assess volunteers/patients for eligibility for research and recruit new patients, to act as a resource to the members of the MDT.

• Ensure that trial specific clinical investigations / procedures are undertaken as required by the research protocol in order to establish eligibility and maintain safety in the trial by all team members.

• Take relevant samples as required by the study protocol such as blood samples, package and dispatch as defined. Ensure safe and appropriate storage of specimens in accordance with trial protocols and regulatory / Trust guidance.

• Ensure all team members undertake relevant training and assessment of competence, working within scope of professional practice prior to undertaking any clinical procedures / administration of treatments associated with the research treatment regimes.

• Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial by all team members.

• Ensure staff monitor treatment toxicity/side effects reporting to the relevant personnel, recording as required assisting in any required changes to treatment as required by the protocol

• Ensure all staff record and report adverse /serious adverse events as classified in the study protocol criteria which occur whilst patient is in the clinical trial e.g. hospital admission since last study visit

• Ensure accurate documentation of patient’s events in nursing/medical notes and study specific case report forms.

• Provide ongoing information, education and support to patients (and their significant others) regarding clinical trials and their care.




Research and Portfolio Management

• Lead in the delivery of studies within the relevant specialities ensuring they meet the requirements with regards to the Department of Health’s Research Governance Framework for Health and Social Care and the EU Clinical Trials legislation by implementing quality systems.

• Assist in the review of study protocols and contribute to the feasibility/study selection process, advising on safety, regulatory and logistical issues.

• Liaise with RD&I Set Up Team staff contributing to the process of gaining local regulatory committee approval where required to ensure efficient service is delivered to sponsors.

• Work with the research teams and investigators to develop strategies to overcome barriers to recruitment and solve other problems relating to specific studies.

• Following appropriate training and competence assessment receive written informed consent from participants for allocated research studies in accordance with study protocol and Trust guidance.

• Following appropriate training and competence assessment act as an assessor for the process of informed consent for research according to Trust guidelines.

• Randomise / enrol patients into clinical trials or other research studies.

• Assess and evaluate the progress of on-going clinical trials and research identifying resource implications for the teams.

• Co-ordinate the monthly local portfolio team performance meetings: identify and act on issues.

• Ensure accurate records for all research projects that are overseen within allocated teams are kept in accordance with all regulatory requirements including the data protection act

• Ensure that all ICH GCP required documentation is kept in a clearly traceable system and is stored in an appropriate manner for the appropriate length of time.

• Provide advice and support to other members of the research and multidisciplinary team with regard to research governance.

• Ensure self and team members respond to data queries generated by the study co-ordinating team within a timely manner.

• Ensure all team members maintain accurate records of study recruitment as per local procedure and status of studies providing regular updates. This will involve ensuring that EDGE (local patient management system) is updated with key trial data and feeding back through the local portfolio team meetings

For further details please see the attached job description.


This advert closes on Monday 27 May 2024

Clinical Work autonomously to manage a caseload of patients acting as a professional to ensure care to patients is delivered according to Trust policies and procedures and the research protocol delivery high standards and continuity of clinical care for study participants. Maintain strong relationships and communication channels with other key personnel such as multidisciplinary teams, clinical wards areas. Attend Multi-disciplinary Meetings, and appropriate clinics, to assess volunteers/patients for eligibility for research and recruit new patients, to act as a resource to the members of the MDT. Ensure that trial specific clinical investigations / procedures are undertaken as required by the research protocol in order to establish eligibility and maintain safety in the trial by all team members. Take relevant samples as required by the study protocol such as blood samples, package and dispatch as defined. Ensure safe and appropriate storage of specimens in accordance with trial protocols and regulatory / Trust guidance. Ensure all team members undertake relevant training and assessment of competence, working within scope of professional practice prior to undertaking any clinical procedures / administration of treatments associated with the research treatment regimes. Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial by all team members. Ensure staff monitor treatment toxicity/side effects reporting to the relevant personnel, recording as required assisting in any required changes to treatment as required by the protocol Ensure all staff record and report adverse /serious adverse events as classified in the study protocol criteria which occur whilst patient is in the clinical trial e.g. hospital admission since last study visit Ensure accurate documentation of patients events in nursing/medical notes and study specific case report forms. Provide ongoing information, education and support to patients (and their significant others) regarding clinical trials and their care. Research and Portfolio Management Lead in the delivery of studies within the relevant specialities ensuring they meet the requirements with regards to the Department of Healths Research Governance Framework for Health and Social Care and the EU Clinical Trials legislation by implementing quality systems. Assist in the review of study protocols and contribute to the feasibility/study selection process, advising on safety, regulatory and logistical issues. Liaise with RD&I Set Up Team staff contributing to the process of gaining local regulatory committee approval where required to ensure efficient service is delivered to sponsors. Work with the research teams and investigators to develop strategies to overcome barriers to recruitment and solve other problems relating to specific studies. Following appropriate training and competence assessment receive written informed consent from participants for allocated research studies in accordance with study protocol and Trust guidance. Following appropriate training and competence assessment act as an assessor for the process of informed consent for research according to Trust guidelines. Randomise / enrol patients into clinical trials or other research studies. Assess and evaluate the progress of on-going clinical trials and research identifying resource implications for the teams. Co-ordinate the monthly local portfolio team performance meetings: identify and act on issues. Ensure accurate records for all research projects that are overseen within allocated teams are kept in accordance with all regulatory requirements including the data protection act Ensure that all ICH GCP required documentation is kept in a clearly traceable system and is stored in an appropriate manner for the appropriate length of time. Provide advice and support to other members of the research and multidisciplinary team with regard to research governance. Ensure self and team members respond to data queries generated by the study co-ordinating team within a timely manner. Ensure all team members maintain accurate records of study recruitment as per local procedure and status of studies providing regular updates. This will involve ensuring that EDGE (local patient management system) is updated with key trial data and feeding back through the local portfolio team meetings For further details please see the attached job description.

The post holder will be responsible for the day to day management of several of the R&D clinical research studies and teams. The post holder will be supporting the safe conduct of research in accordance with the regulatory and legal frameworks relating to the planning, undertaking and closure of research studies providing assurance that the rights and well being of trial participants are protected.

Excellent support from the close-knit management team will be provided including a comprehensive induction package and the opportunity to really develop as a manager and leader of a patient focused, quality driven, cutting-edge service.

The post holder will be instrumental in implementing team objectives to enhance the performance and development of the research teams whilst providing guidance, education, leadership and co-ordinating the portfolio of research studies and clinical trials to deliver high quality research and clinical care.

The role integrates both clinical duties such as maintaining an active caseload and managerial duties; as such the post holder will be required to effectively manage their time to fulfil key responsibilities. It is also expected that the post holder will be flexible with hours of work as required to ensure that we are offering a service that best suits the needs of our patients.

The post holder will be employed by Research and Development department (R&D) to work within the central clinical research teams, managing an allocated number of research teams.

However, it is expected that the post folder will work flexibly across other research speciality areas as service requirements dictate throughout the duration of their contract.

The post holder will be responsible for the day to day management of several of the R&D clinical research studies and teams. The post holder will be supporting the safe conduct of research in accordance with the regulatory and legal frameworks relating to the planning, undertaking and closure of research studies providing assurance that the rights and well being of trial participants are protected.

The job holder may be required to carry out other similar or related duties within their bounds of registration which do not fall within the work outlined which may reasonably be required to deliver a comprehensive research service to our patients. The Line Manager, in consultation with the post holder will undertake any review.

University Hospitals Coventry and Warwickshire NHS Trust, rated as good by the Care Quality Commission, is one of the largest teaching Trusts in the UK.

We are extremely proud of our employees across our hospital sites, with high quality patient care at the heart of everything we do.

Boasting some of the most modern facilities in Western Europe, the Trust is renowned for being at the forefront of research and innovation as part of its blossoming reputation as a worldwide leader in healthcare.

We are proud to be recognised as a Pathway to Excellence®designated organisation – please click the link for further details about this prestigious award.Pathway To Excellence ® - University Hospitals Coventry & Warwickshire (uhcw.nhs.uk)

By joining our exciting journey, you will form part of a passionate, talented team and will be able to access a wide range of learning and development opportunities. There has never been a better time to join our team.

The Trust is committed to building an organisation that makes full use of the talents, skills, experience, and different perspectives available in our diverse society. We want everyone to feel they are respected, valued, can achieve their potential and receive the most appropriate and relevant care. We will create an environment where the equality and human rights principles of fairness, respect, equality, dignity and autonomy are promoted and are part of the organisation's core values.

Clinical

• Work autonomously to manage a caseload of patients acting as a professional to ensure care to patients is delivered according to Trust policies and procedures and the research protocol delivery high standards and continuity of clinical care for study participants.

• Maintain strong relationships and communication channels with other key personnel such as multidisciplinary teams, clinical wards areas.

• Attend Multi-disciplinary Meetings, and appropriate clinics, to assess volunteers/patients for eligibility for research and recruit new patients, to act as a resource to the members of the MDT.

• Ensure that trial specific clinical investigations / procedures are undertaken as required by the research protocol in order to establish eligibility and maintain safety in the trial by all team members.

• Take relevant samples as required by the study protocol such as blood samples, package and dispatch as defined. Ensure safe and appropriate storage of specimens in accordance with trial protocols and regulatory / Trust guidance.

• Ensure all team members undertake relevant training and assessment of competence, working within scope of professional practice prior to undertaking any clinical procedures / administration of treatments associated with the research treatment regimes.

• Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial by all team members.

• Ensure staff monitor treatment toxicity/side effects reporting to the relevant personnel, recording as required assisting in any required changes to treatment as required by the protocol

• Ensure all staff record and report adverse /serious adverse events as classified in the study protocol criteria which occur whilst patient is in the clinical trial e.g. hospital admission since last study visit

• Ensure accurate documentation of patient’s events in nursing/medical notes and study specific case report forms.

• Provide ongoing information, education and support to patients (and their significant others) regarding clinical trials and their care.




Research and Portfolio Management

• Lead in the delivery of studies within the relevant specialities ensuring they meet the requirements with regards to the Department of Health’s Research Governance Framework for Health and Social Care and the EU Clinical Trials legislation by implementing quality systems.

• Assist in the review of study protocols and contribute to the feasibility/study selection process, advising on safety, regulatory and logistical issues.

• Liaise with RD&I Set Up Team staff contributing to the process of gaining local regulatory committee approval where required to ensure efficient service is delivered to sponsors.

• Work with the research teams and investigators to develop strategies to overcome barriers to recruitment and solve other problems relating to specific studies.

• Following appropriate training and competence assessment receive written informed consent from participants for allocated research studies in accordance with study protocol and Trust guidance.

• Following appropriate training and competence assessment act as an assessor for the process of informed consent for research according to Trust guidelines.

• Randomise / enrol patients into clinical trials or other research studies.

• Assess and evaluate the progress of on-going clinical trials and research identifying resource implications for the teams.

• Co-ordinate the monthly local portfolio team performance meetings: identify and act on issues.

• Ensure accurate records for all research projects that are overseen within allocated teams are kept in accordance with all regulatory requirements including the data protection act

• Ensure that all ICH GCP required documentation is kept in a clearly traceable system and is stored in an appropriate manner for the appropriate length of time.

• Provide advice and support to other members of the research and multidisciplinary team with regard to research governance.

• Ensure self and team members respond to data queries generated by the study co-ordinating team within a timely manner.

• Ensure all team members maintain accurate records of study recruitment as per local procedure and status of studies providing regular updates. This will involve ensuring that EDGE (local patient management system) is updated with key trial data and feeding back through the local portfolio team meetings

For further details please see the attached job description.


This advert closes on Monday 1 Apr 2024

Clinical Work autonomously to manage a caseload of patients acting as a professional to ensure care to patients is delivered according to Trust policies and procedures and the research protocol delivery high standards and continuity of clinical care for study participants. Maintain strong relationships and communication channels with other key personnel such as multidisciplinary teams, clinical wards areas. Attend Multi-disciplinary Meetings, and appropriate clinics, to assess volunteers/patients for eligibility for research and recruit new patients, to act as a resource to the members of the MDT. Ensure that trial specific clinical investigations / procedures are undertaken as required by the research protocol in order to establish eligibility and maintain safety in the trial by all team members. Take relevant samples as required by the study protocol such as blood samples, package and dispatch as defined. Ensure safe and appropriate storage of specimens in accordance with trial protocols and regulatory / Trust guidance. Ensure all team members undertake relevant training and assessment of competence, working within scope of professional practice prior to undertaking any clinical procedures / administration of treatments associated with the research treatment regimes. Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial by all team members. Ensure staff monitor treatment toxicity/side effects reporting to the relevant personnel, recording as required assisting in any required changes to treatment as required by the protocol Ensure all staff record and report adverse /serious adverse events as classified in the study protocol criteria which occur whilst patient is in the clinical trial e.g. hospital admission since last study visit Ensure accurate documentation of patients events in nursing/medical notes and study specific case report forms. Provide ongoing information, education and support to patients (and their significant others) regarding clinical trials and their care. Research and Portfolio Management Lead in the delivery of studies within the relevant specialities ensuring they meet the requirements with regards to the Department of Healths Research Governance Framework for Health and Social Care and the EU Clinical Trials legislation by implementing quality systems. Assist in the review of study protocols and contribute to the feasibility/study selection process, advising on safety, regulatory and logistical issues. Liaise with RD&I Set Up Team staff contributing to the process of gaining local regulatory committee approval where required to ensure efficient service is delivered to sponsors. Work with the research teams and investigators to develop strategies to overcome barriers to recruitment and solve other problems relating to specific studies. Following appropriate training and competence assessment receive written informed consent from participants for allocated research studies in accordance with study protocol and Trust guidance. Following appropriate training and competence assessment act as an assessor for the process of informed consent for research according to Trust guidelines. Randomise / enrol patients into clinical trials or other research studies. Assess and evaluate the progress of on-going clinical trials and research identifying resource implications for the teams. Co-ordinate the monthly local portfolio team performance meetings: identify and act on issues. Ensure accurate records for all research projects that are overseen within allocated teams are kept in accordance with all regulatory requirements including the data protection act Ensure that all ICH GCP required documentation is kept in a clearly traceable system and is stored in an appropriate manner for the appropriate length of time. Provide advice and support to other members of the research and multidisciplinary team with regard to research governance. Ensure self and team members respond to data queries generated by the study co-ordinating team within a timely manner. Ensure all team members maintain accurate records of study recruitment as per local procedure and status of studies providing regular updates. This will involve ensuring that EDGE (local patient management system) is updated with key trial data and feeding back through the local portfolio team meetings For further details please see the attached job description.

The Research Sr Associate is a seasoned professional role. Applies in-depth disciplinary knowledge, contributing to the development of new techniques and the improvement of processes and work-flow for the area or function. Integrates subject matter and industry expertise within a defined area. Requires in-depth understanding of how areas collectively integrate within the sub-function as well as coordinate and contribute to the objectives of the function and overall business. Evaluates moderately complex and variable issues with substantial potential impact, where development of an approach/taking of an action involves weighing various alternatives and balancing potentially conflicting situations using multiple sources of information. Requires good analytical skills in order to filter, prioritize and validate potentially complex and dynamic material from multiple sources. Strong communication and diplomacy skills are required. Regularly assumes informal/formal leadership role within teams. Involved in coaching and training of new recruits. Significant impact in terms of project size, geography, etc. by influencing decisions through advice, counsel and/or facilitating services to others in area of specialization. Work and performance of all teams in the area are directly affected by the performance of the individual.

Responsibilities:

• Citi Research focuses on delivering high quality investment insights to investors on a global basis with a high emphasis on independence and objectivity in its products and insights
• The unit produces regular written research, hosts investor meetings with company management teams, holds conference calls with industry consultants and regularly communicates with clients (both internal and external)
• Modeling: Maintaining & updating existing company models; creating new models; maintaining relative value sheets
• Research: Assist with the publication of earnings previews/recaps, initiation reports, deep dive notes as well other group products
• Communication: Assist with client inquires and requests (internal and external)
• Events: Assist with coordination of investor meetings (management meeting & field trips) and conference calls with consultants
• Appropriately assess risk when business decisions are made, demonstrating particular consideration for the firm's reputation and safeguarding Citigroup, its clients and assets, by driving compliance with applicable laws, rules and regulations, adhering to Policy, applying sound ethical judgment regarding personal behavior, conduct and business practices, and escalating, managing and reporting control issues with transparency.

Qualifications:

• 2-4 years previous experience
• MBA or graduate degree and/or CFA preferred.
• Experience in Sell-Side Research and/or in a relevant industry
• Good knowledge of accounting and modelling with a credit focus
• Experience in supporting senior research analysts
• Excellent inter-personal and writing skills
• Attention to detail
• Secure and maintain applicable licenses

Education:

• Bachelor’s/University degree or equivalent experience

Salary Range for NYC: $150,000 - $175,000

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Job Family Group:

Research

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Job Family:

Research Analysis

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Time Type:

Full time

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Primary Location:

New York New York United States

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Primary Location Full Time Salary Range:

$45,440.00 - $205,200.00

In addition to salary, Citi’s offerings may also include, for eligible employees, discretionary and formulaic incentive and retention awards. Citi offers competitive employee benefits, including: medical, dental & vision coverage; 401(k); life, accident, and disability insurance; and wellness programs. Citi also offers paid time off packages, including planned time off (vacation), unplanned time off (sick leave), and paid holidays. For additional information regarding Citi employee benefits, please visit citibenefits.com. Available offerings may vary by jurisdiction, job level, and date of hire.

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Anticipated Posting Close Date:

Mar 18, 2024

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Citi is an equal opportunity and affirmative action employer.

Qualified applicants will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

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