Total 327 Science / R&D / Research job vacancies in Queenstown

Company: Academic Institution (West)

Agency contract: 6 months

Up to $4500

Job Description

• Manages research grant applications and awarded grants
• Acts as SAP Concur reviewer and first-level approver, collaborating with Finance for efficient approval processes
• Creates weekly research e-newsletters to share internal and external grant opportunities with faculty and staff
• Develops content for the school’s website and research-related publications (brochures, pamphlets)
• Assists in organizing the monthly research talks
• Monitors research grant budgets, expenditures, and deadlines for reports

Specific Requirements:

• Bachelor's degree
• Strong administrative skills with accurate data handling.
• Proficient in reporting with some finance knowledge.
• Min. 2 years of relevant experience, preferably in an academic setting.
• Excellent interpersonal, communication, and analytical skills.
• Strong organizational and problem-solving abilities.
• Proficient in Microsoft Office (Excel, PowerPoint, Word).
• Experience in content management and creation (website, social media, newsletters).

Annabelle Quek, ITT Team

Reg No: R21102691 EA: 05C3053

BGC Group Pte Ltd

Key Responsibilities

• Issue and manage client invoices, submit electronic invoices, and monitor overdue accounts.
• Update cash flow forecasts and perform accounts receivable reconciliations.
• Reconcile intercompany transactions and ensure accuracy in month-end balances.
• Prepare and post recurring monthly journal entries.
• Prepare monthly management reporting package, including variance analysis and financial performance summaries.
• Assist the Finance Director with Transfer Pricing compliance and planning of tax and transfer pricing strategies for local and regional portfolios.
• Prepare quarterly GST (Goods and Services Tax) computations.
• Prepare estimated corporate income tax computations.
• Liaise with external auditors, corporate secretaries, and tax agents as needed.
• Prepare full sets of dormant subsidiary accounts.
• Support the annual J-SOX audit conducted by external auditors.
• Assist the Finance Director with any other ad hoc duties as assigned.

Job Requirements

• Bachelor’s Degree/Post Graduate Diploma/Professional Degree in Finance, Accountancy, or a related field.
• At least 5 years of relevant working experience in full-set accounting.
• Proficient in Microsoft Excel and pivot tables.
• Experience with MYOB or ERP systems.
• Knowledge of J-SOX and FRS reporting requirements.

To provide research support service for Nursing clinical research. He/she works closely with the Principal Investigator (PI) and members of the Nursing Research Team.

Main responsibilities:
• To assist in Institutional Review Board applications
• To assist in screening of participants for recruitment
• To assist in enrolling participants into the clinical study
• To organize participants’ visits, and ensure that all the required procedures are carried out
• To collect data and complete clinical reports
• To record and report adverse events
• To assist in maintaining and organization of study site file
• To assist the investigators in conducting clinical trial according to Good Clinical Practice guidelines.
• To communicate closely with the sponsor company and the investigators and provide ancillary services for the clinical trials.
• To ensure all study-related activities are carried out efficiently and coordinate project meetings.
• To participate in the preparation of abstracts, posters and manuscripts for dissemination of study results as well as reports as required by the funder.
• Other duties as specified by Department Head or Supervisor.

Job requirements:
• Bachelor in Science, Health Science, Nursing or a related field
• Good knowledge of computer applications e.g. Microsoft Access and Excel, PowerPoint, SPSS
• Team-oriented with strong coordination and organisational skills
• Excellent oral and written communication skill
• Excellent interpersonal skill
• Good time management skill

Major Duties and Responsibilities

• Conduct patient recruitment and collection of primary and/or secondary data
• Ensure study is managed and all study documents are kept in order
• Assist Principal Investigator in the implementation of study plans and schedule
• Maintain department's clinical audit databases
• Provide administrative support for studies under Principal Investigator

Job requirements:

• Diploma holder preferably with nursing, biomedical science, life science background or related fields
• Good verbal and written communication skill is required
• Good problem-solving skills
• Good interpersonal skills and ability to work both independently and in a team
• Good knowledge of MS Office software including excel,access, powerpoint, word

Requirement

Design, build, and enhance responsive web and mobile applications using modern frameworks and technologies such as ReactJs, NextJs, Vuejs, NodeJs, Django, Flutter, and Riverpod.

Implement and manage efficient database structures and APIs for data retrieval and manipulation, ensuring high performance and scalability.

Work closely with team members to ensure timely delivery of products. Communicate effectively with team leads and stakeholders to gather requirements and provide regular updates.

Write clean, maintainable, and well-documented code. Stay updated with current web technologies and industry best practices to ensure high-quality software development.

Apply UI requirements using modern design tools and libraries, ensuring user-friendly and aesthetically pleasing interfaces across web and mobile platforms.

Analyze and address complex problems, propose solutions, and present ideas for continuous improvement. Adapt to evolving project requirements and technology trends.

Requirement

• Design, build, and enhance responsive web and mobile applications using modern frameworks and technologies such as ReactJs, NextJs, Vuejs, NodeJs, Django, Flutter, and Riverpod.
• Implement and manage efficient database structures and APIs for data retrieval and manipulation, ensuring high performance and scalability.
• Work closely with team members to ensure timely delivery of products. Communicate effectively with team leads and stakeholders to gather requirements and provide regular updates.
• Write clean, maintainable, and well-documented code. Stay updated with current web technologies and industry best practices to ensure high-quality software development.
• Apply UI requirements using modern design tools and libraries, ensuring user-friendly and aesthetically pleasing interfaces across web and mobile platforms.
• Analyze and address complex problems, propose solutions, and present ideas for continuous improvement. Adapt to evolving project requirements and technology trends.

Purpose

The candidate will participate in clinical research projects in SERI related to Glaucoma, including examination of study participants, collection andorganization of clinical and imaging data in order to characterize the underlying disease mechanisms of the disease and to determine the factors associated with disease progression. The candidate will receive appropriate mentoring support by the senior members of the team, with the aim to produce high impact factor articles in ophthalmic and visual science. You will assist the Principal investigator and other team members in the successful execution of the project(s).

Duties andResponsibilities

The Research Component includes the following:

• To conduct and coordinate clinical research in glaucoma diseases within SERI/SNEC in line with its research strategy, including PI-initiated studies and industry sponsored clinical trials
• To assist in management of these research projects, which includes supervising post-doctoral research assistants, research students, technical and other support staff
• To co-ordinate and ensure smooth running of the study at the study site/s
• To publish research outcomes in appropriate journals of international standing and to publish and disseminate the result of research and scholarship in other reputable outlets
• To attend and present research findings and papers at academic and professional conferences, and to contribute to the external visibility of the department
• To help draft research reports for the Director, Principal Investigators
• To undertake such specific roles and management functions as may be reasonably required by the Director, Principal Investigators
• To attend meetings and to participate (where necessary) in other committees and working groups within SERI/SNEC
• To ensure compliance with health and safety in all aspects of work
• To assist the Principal Investigators with grant applications
• Any other duties as assigned by the Director, Principal Investigators

The Clinical Component includes the following:

• To review and counsel patients on the disease
• To assist Principal Investigators in recruitment of subjects, conduct Informed Consent and eligibility checks

Requirement

• MMed (Ophthalmology), FRCS or its equivalent, registrable with the Singapore Medical Council
• Completed 2 years of advance training rotations in general ophthalmology
• Experienced in most aspects of clinical ophthalmology and competent with intravitreal injections. Experience in Imaging papers will be an added advantage
• A demonstrated familiarity with principles of clinical research studies
• Able to work independently and multi-task

Job Responsibilities:

• Implementing the program for the class in accordance with the policies, guidelines, framework and philosophy of the centre.
• Guiding primary school children (primary 1 to 6) to ensure completion of daily homework
• Keeping accurate records of children’s progress and address each child’s educational and developmental needs on an individual basis to the best of your ability.
• Prepare and upkeep of teaching resources, arrangement, appearance and learning environment of the classroom.
• Maintain and build relationships with children and parents.
• Conducting MindChamps unique enrichment programmes.
• Being an inspiring role model with a creative spirit and a champion (positive) mindset.
• Use positive discipline techniques at all times.
• Ensure safety and timely transfer of students from school to student centre
• Ensure safety of children within the premises
• Any other ad-hoc duties as delegated by Centre Director/ Manager

Job Requirements:

• Diploma in any discipline
• Experience in teaching primary school students will be an advantage
• Able to guide in doing primary school subjects
• Possess good communication and classroom management skills.
• Enthusiastic & energetic and has a positive mindset to learn and grow together with the company.
• Creative and loving energy with a positive disposition
• Excellent communication and classroom management skills

You will be responsible for harvesting of tissues, providing histological examination of frozen and paraffin-embedded material, and overseeing the day-to-day tissue harvesting from operation theatres. You will assist the supervisor in research services to the researchers.

Your responsibilities will include:

- Biospecimen processing such as collection, processing of blood, inventory stock taking and administrative support.

- Tissue bank procesing and ensure compliance to bio-safety procedures and IRB regulations for the handling of human tissues.

- Consent taking.

- Oversee the processing, storage and retrieval of harvested materials.

- Work with the tissue bank committee and colleagues to implement cluster-wide policies & procedures governing tissue collection and handling.

- Assist in NCCS-SB application regards to researcher study and criteria of the project.

- Administrative support for the related research services.

Requirements:

- Medical degree (MD or equivalent) from a reputable medical school.

- Completed an approved residency in anatomic pathology and experience in clinical pathology will be a bonus.

- At least 3 years of relevant clinical experience in anatomic pathology.

- Laboratory experience in specimen cut-up and histological techniques such as tissue processing, microtomy and staining.

- Experience in immunohistochemistry and molecular biology will be a bonus.

- Good working knowledge of local regulatory requirements.

- Meticulous, with excellent organizational and time management skills.

- Good communication, organizational and interpersonal skills.

- Ability to complete tasks independently with minimal supervision.

- Ability to work independently and make reliable recommendations and diagnoses.

- Ability to work on multiple projects and interact effectively with clinicians, researchers, academicians, administrators, and external and internal stakeholders.

The Associate Clinical Research Coordinator (ACRC) shall assist all levels of Clinical Research Coordinators (CRCs and above), in coordinating clinical research.

The ACRC has to ensure that trial- related work is conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials Office Standard Operating Procedures (SOPs) as well as instructions from her superiors.

You will support and assist in the following trial related activities:

• Take over trials that have completed treatment phase or trials that involve few simple procedures.
• Data collection and management including resolving data discrepancies, tracking of trial expenditures and timely invoicing (where applicable), etc.
• Administering quality of life questionnaires or any other surveys as and when required.
• Performing trial procedures which include taking and recording patients’vital signs performing ECGs; collecting data; other trial-related procedures.
• Collection and delivery of biological specimens eg blood, urine and tissues whenever necessary.
• Inventory of study materials such as laboratory kits, patient diaries and case report forms to ensure adequate supplies are maintained to conduct the trials.
• Collection of medical records or duplicate radio-diagnostic films and ensuring that the items are collected in accordance with specific request forms.
• Managing the Clinical Trials Office’s Medical Records Trolley and the transportation of medical notes in the Trolley between Medical Records Office and the Clinical Trials Office. The ACRC shall also assist other CTO staff to obtain medical notes and other source documents.

Requirements:

• Diploma in Life Sciences/Nursing
• Proficient at performing venepuncture for blood specimen collection
• 2 years of related working experience an advantage
• Knowledge in cannulation would be an added advantage
• Good time-management and communication skills
• Able to work independently and detailed oriented
• Computer literate

The National Heart Research Institute Singapore, based at the National Heart Centre Singapore, is currently offering a job opportunity to work with our Clinician Scientist in the area of cardiac imaging. The applicant needs to have experience in computer programming and be comfortable working with large imaging datasets coupled with multi-omics. There will also be opportunities to work with magnetic resonance physicist in sequence programming.

Requirements

· BSc or MSc in computer science or related

· Experience in image processing and analysis in cardiac MRI is preferred

· A team player and also able to work independently, demonstrating effective collaboration skills

Asian Thoracic Oncology Research Group (ATORG) is the coordinating platform for translational research for thoracic malignancies in Asia. Its mission is to advance medical knowledge of lung cancer and improve health outcomes of patients through clinical studies and scientific events.

Asia Pacific Oncology Drug Development Consortium (APODDC) was formed to foster education and collaboration between key stakeholders of cancer drug development within the Asia Pacific region, thereby improving treatment access to patients. APODDC drives regional activities in collaboration with institutions in the region and industry partners.

ATORG and APODDC operate centrally under the Clinical Trials and Epidemiological Sciences (CTE) division in National Cancer Centre Singapore.

The Senior / Executive will mainly organise events for ATORG and APODDC . The types of events include, but are not limited to, virtual, hybrid and in-person advisory board meetings, educational seminars and workshops. This role provides opportunities to interact internationally with healthcare institutions, industry partners and vendors, and manage key stakeholders at a regional level.

Main Responsibilities:

Organise events (60%)

• Responsible for managing events from startup to execution
• Communicate effectively and manage internal and external stakeholders and service providers
• Plan timeline for each event
• Draft budget, including sourcing of funding and reconciliation of funding and expenses
• Handle all logistics, inclusive of procurement (eg. venue, online/travel arrangements) and on-site management during event
• Develop marketing materials such as posters and collaterals and for social media
• Write meeting minutes, if required
• Administer pre- and post-event follow ups
• Manage agreements between key stakeholders, vendors and industry partners
• Manage manuscripts from drafting to publication.

ATORG Operations (30%)

• Manage operational duties of ATORG; this includes procurement of stationery and devices, collating of department information, updating of mailing list.
• Act as a liaison for department administrative matters

Other Duties (10%)

• Assist in any other work as assigned, which may include administrative tasks

Requirements:

• Degree, preferably in life sciences
• At least 1-2 years of events organisation experience, preferably in healthcare/ scientific research
• Candidates with experience organising school or external curricular events are welcome to apply!
• Candidates with more experience will be considered for the Senior Executive Role
• Meticulous with close attention to timelines
• Able to handle multiple priorities independently
• Able to work with tight deadlines
• Strong organisational skills
• Strong interpersonal skills

The Asian Thoracic Oncology Research Group (ATORG) was formed in 2016 to be the central coordinating platform for translational research and multi-centre clinical trials for thoracic malignancies in the Asia Pacific region. It is hosted by National Cancer Centre Singapore.

The Executive will provide administrative support mainly for the ATORG team and the Principal Investigator (PI) in other aspects outside of ATORG. This role provides opportunities to interact internationally with healthcare institutions, industry partners and vendors, apart from internal functions.

Key Accountabilities:

• Administrative Support: Provide day-to-day administrative support including managing PI’s schedules, reimbursements, handling correspondence, minutes taking and organizing meetings with internal team and external committee meetings with Key Opinion Leaders (KOLs) of ATORG’s network in APAC.
• Travel Arrangements: Organize and coordinate travel plans, accommodations, and itineraries for PI and KOLs.
• Office Management: Oversee office supplies inventory, ensuring availability and placing orders when necessary
• Communication: Act as the point of contact for internal and external communications, ensuring messages are relayed efficiently.
• Assistance with research administration, which may include grant management (application, tracking of progress, reporting), purchase requisitions, consultancy agreements and documentation for scientific activities
• Coordination: Coordinate with different departments, vendors, and external partners to facilitate smooth operations. Assist in the planning and execution of education events, board meetings, and conferences. Able to work with external event agencies.

Requirements:

• Degree in Biomedical/Life Sciences with at least 1 year of similar working experience
• Meticulous and fast worker with close attention to timelines
• Strong organisational skills
• Good interpersonal skills
• Committed team player
• Fluent in both written and spoken English.

The Clinical Research Coordinator (CRC) shall help investigators conduct mainly investigator-initiated clinical trials. The CRC has to ensure that clinical trials are conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials Operations’ Standard Operating Procedures.

Key Responsibilities:

• Accomplish the study’s target enrolment as per agreed study timelines or shorter through effective recruitment strategies.
• Regular discussion or follow-up with study team on subject screening & recruitment rates eg. email communication or team meetings with Drs.
• Timely response/followup to email enquiries within 10 working days or less.
• Foster good working relationships and collaborate effectively across all streams to promote operational efficiency
• Invoicing is carried out on time and payment can be received with minimal delays.

Key Requirements:

• Degree in Nursing, Degree in Medicine, Pharmacy or Healthcare / biological sciences, preferably with experience in clinical trials or clinical research.
• 1-2 years experience in the conduct of clinical trials, specializing in Heamatology / Oncology interventional trials, governed under Health Product Act.
• Must have knowledge of setting up cell therapy trials.
• Must already been trained in ICH GCP.
• Meticulous and possesses good organizational and time management skills.
• Good communication and interpersonal skills.
• Independent learner, Meticulous and possesses good organizational and time management skills.
• Team player and work well with external collaborators and partners.
• Proactive in learning and helping other CRCs in issues with trial management

Key Responsibilities:

• Provides effective administration of research grant call applications and management of awarded grants
• Assumes the role as SAP Concur reviewer and first-level approver and work with the Finance department to provide the fastest and smoothest approver flow.
• Creates weekly research e-newsletter to communicate information on internal and external grant calls to staff members.
• Develops content for the company’s website for research grants, projects and achievements.
• Develops Research-related publications (Research Brochures /Pamphlets)
• Assists with the organisation of the monthly organized talks
• Monitor budgets and expenditures relating to research grants
• Monitor deadlines for the submission of expenditure reports as well as progress and final reports

Requirements:

• Bachelor's degree from a recognised university
• Proven administrative skills including the ability to handle data with accuracy.
• Excellent reporting with some finance working knowledge would be essential.
• Preferably 2 to 3 years of relevant work experience. Prior working experience in an academic institution will be an advantage.
• Sound interpersonal, communication and analytical skills.
• Strong organisational and problem-solving skills.
• Competency in Microsoft Office applications (Excel, PowerPoint, word).
• Ability to do content management and creation of information on research (Website, social media and newsletters)
• Positive attitude with a strong desire to learn new skillsets.

Khaty Zainal

R22111204

BGC Group Pte Ltd(Outsourcing)

EA05C3053