Total 41 Science / R&D / Research job vacancies in Hyderabad, Telangana

Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials.

Job Summary

Provide statistical programming support to clinical trials. Produce statistical analyses, including generating/validating analysis datasets, tables, listings, and figures for clinical trials. Create SDTM mapping and datasets. Develop and maintain the infrastructure for project files of SAS datasets and SAS code. Support Data Management in data set creations/transfers, integrity checks, and quality audits. Act as a liaison between clinical and subcommittees and project teams on an as-needed basis.

Primary Responsibilities

• Perform or oversee team in performing all statistical programming required for clinical trial analysis and reporting on large scale projects of high complexity

• Apply appropriate statistical methods for data analysis and provide statistical programming expertise for project teams

• Review the Statistical Analysis Plan in preparation for programming the planned analyses

• Lead design/development of SAS macros and other utilities to expedite SAS programming activities

• Organize and conduct internal training sessions and author papers for conferences

• Generate tables, listings, and figures per protocol, Statistical Analysis Plan, and/or approved client request

• Participate in statistical program validation and quality control activities

• Develop or review SDTM aCRF and specifications, ADaM specifications; complete programming and validation of CDISC SDTM and ADaM datasets

• Review pinnacle 21 reports and ensure compliance with CDISC and FDA guidelines

• Develop define.xml, study data reviewers guide and analysis datasets reviewers guide

• Identify study priorities and communicate effectively with project team and management

• Ensure quality, proper documentation and meet or exceed timely completion of the project within budgeted hours

• Manage statistical programming timelines, budgets, and client expectations

• Actively participate in study team meetings

• Interact with other departments, such as Clinical Operations, Project Management, and Data Management to ensure a high level of client satisfaction through successful execution of projects

• Participate in review process of study documents such as the CRF, edit check specifications, and database design specifications written by Data Management

• Program data cleaning checks, as necessary, to assist Data Management’s data cleaning activities

• Participate in installation/validation of statistical software packages throughout the software development lifecycle

• Develop and maintain the infrastructure for project files of SAS datasets and SAS code

• Mentor junior level statistical programmers by developing training plans and providing oversight of their work Ensure all programming activities and processes performed are conducted according to SDC’s standard procedures and/or sponsor requirements

• Adhere to all aspects of the SDC’s quality system

• Comply with SDC’s data integrity & business ethics requirements

• Perform other related duties incidental to the work described herein

• Adherence to all essential systems and processes that are required at SDC to maintain compliance to business and regulatory requirements

The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.

Required Skills

• Strong analytical skills, with the ability to process scientific and medical data.

• Very strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat, SAS Macros and SAS/Graph

• Strong problem-solving skills

• Able to work independently

• Excellent knowledge of statistical programming

• Proficient in manipulating and analyzing SAS data

• Ability to identify data issues, present problems, and implement solutions quickly

• Capability of communicating technical concepts clearly, concisely, and understandably to non-statistical colleagues

• Good organizational and time management skills, with the ability to multi-task

• Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP). Expert knowledge of CDISC SDTM and ADaM data models

• Very strong interpersonal communication, presentation, and leadership skills

• SAS Base, Advance and Clinical Trials Certification is preferred

Education or Equivalent Experience

Bachelor’s degree in computer science, statistics or other related, scientific field and at least eight years of relevant professional experience; or an equivalent combination of relevant education and/or experience.

Why SDC

SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances and positive work/life balance, we are able to attract some of the most talented people in the industry.

• We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits.

• We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment.

• We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.

• We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry.

• With a proven track record, SDC has been successfully executing client clinical programs since 2005.

Take a look at how you can join our team!

#LI-Hybrid

Roles & Responsibilities
 

1. To provide scientific support to analysts at bench level for developing & qualifying methods required for product Analytics.
2. Execution of critical experiments for specific deliverables.
3. Ensuring error free analysis and documentation.
4. Ensuring timely and effective review of HPLC/UPLC calibration and maintenance of equipment/ instruments/columns.
5. Drafting Method Development Reports, Method Qualification Report, Biosimilarity, comparability reports
6. Participation in Quality related initiatives, activities and their timely closures.
7. To plan for procuring of appropriate consumables and reagents required for the work and maintain the inventory proactively for critical Reference standards
8. Involve in report preparations, report closures and technology transfer of assays. To ensure timely coordination of stability time point and report closure.

Job Summary
We are seeking a highly skilled Analytical Scientist to join our Research and Development team. The successful candidate will be responsible for developing, validating, and implementing analytical methods for the quantification and identification of genotoxic impurities in pharmaceutical products. This role will involve extensive use of chromatography techniques and adherence to regulatory standards. The ideal candidate should have a strong background in analytical chemistry, method development, and data analysis, with a keen eye for detail and a commitment to ensuring the highest quality standards.

Roles & Responsibilities

• You will be responsible to develop and optimize chromatography-based methods for accurately quantifying related impurities in Various stages like KSM, Intermediates and API  genotoxic impurities in various samples.
• You will be responsible to perform R&D samples analysis by using various analytical techniques like HPLC, UPLC, GC,IR , KF ....etc.
• You will be responsible to address regulatory deficiency queries concerning the analytical methods and data related to genotoxic impurities.
• You will be responsible to ensure the quality and accuracy of reference standards and working standards used in analytical testing and method development.
• You will be responsible to develop analytical methods, conduct validation studies to ensure the accuracy and reliability of the methods, and transfer validated methods to the Quality Control (QC) department.
• You will be responsible to prepare comprehensive reports documenting method development, validation results, and any forced degradation studies performed.
• You will be responsible to conduct forced degradation studies to identify potential impurities and establish their chemical nature and behaviour.
• You will be responsible to perform real-time analysis of samples during product development stages to ensure product quality and consistency.
• You will be responsible for compilation of Stability Data to assess the stability profile of the products under various conditions.
• You will be responsible to source and manage the procurement of necessary chemicals, solvents, columns, and other laboratory equipment.
• You will be responsible to ensure proper maintenance of laboratory equipment as per Good Laboratory Practices (GLP) standards to guarantee accurate and reliable results.
• You will be responsible to calibrate instruments as per the calibration schedule and strictly follow Standard Operating Procedures (SOPs) to maintain consistency and accuracy.
• You will be responsible to maintain a clean and organized work area, and ensure that the laboratory environment is controlled at the required temperature for optimal analytical conditions.
• You will be responsible to keep all relevant documents well-maintained and organized for easy access and compliance with internal and external auditing requirements. 

Principal Clinical Programmer (RAVE EDC)

Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials.

Job Summary

Lead in the evaluation, implementation, and validation of packaged systems. Create, maintain, and oversee processes for providing end user support in EDC systems. Build studies and support other users to build studies in EDC and other GxP systems. Works as part of a project team to design and implement clinical database applications in support of clinical research and biostatistics analysis. Processes database programming change requests. Documents all work fully according to FDA regulations and guidances, and company SOPs. Actively promotes standards for the development and acquisition of, and serve as the SME for, GxP systems. Mentors/trains junior level clinical programmers.

Primary Responsibilities

·       Lead the development, validation, and maintenance of clinical databases for clinical trials using a variety of validated software applications

·       Provide complete and accurate documentation of study databases consistent with company standard operating procedures (SOPs), study protocols and related data management plans

·       Develop and maintain global library of clinical database forms, edit checks, and other regularly used programs and routines

·       Implement and test data quality checks in accordance with the study data validation manual

·       Manage and develop programs for the reconciliation of external data from vendors (e.g., central lab data)

·       Serves as SME and facilitates integration of EDC systems to other clinical platforms such as CTMS, Reporting, IRT as needed

·       Assist in managing and updating medical coding dictionaries, including but not limited to MedDRA and WHODrug

·       Oversee the management of EDC, other GxP system user accounts and other help desk activities

·       Track issues in EDC systems, work with EDC vendors to resolve, and escalate issues appropriately to senior management.

·       Quickly learn new and/or advancements in software to become the SME for any technical question

·       Demonstrate good problem-solving skills, a proactive approach, and a willingness to make decisions, seeking advice when necessary

·       Facilitate and/or participate in writing departmental documentation (e.g., training documents, process guidance)

·       Exhibit good time management and organization skills; the ability to work in an efficient manner and prioritize tasks to meet tight deadlines while maintaining the highest standards of work

·       Keep management team abreast of issues, progress, and risks related to trial operations

·       Support bid defenses from a technical SME perspective

·       Participate in other clinical programming and data management activities, as required

·       Participate in internal and external team meetings, as required

·       Mentor junior level clinical programmers

·       Adhere to all aspects of the Statistics & Data Corporation’s quality system

·       Comply with Statistics & Data Corporation’s data integrity & business ethics requirements

·       Perform other related duties incidental to the work described herein

The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.

Required Skills

·       At least eight years’ experience assuming lead database programming responsibilities on projects, with a minimum of 5 years in a clinical environment

·       Excellent understanding of relational database structures

·       Fast, accurate programming skills using assorted application software

·       PL/SQL, SQL, and XML programming skills

·       Solid interpersonal skills, with the ability to work well with people of all levels of expertise and comfort in varied organizational relationships

·       Demonstrated ability to provide both “user-friendly” and technical documentation

·       Ability to provide expertise to guide department in continued efficiency and growth

·       Knowledge and experience with FDA regulations and guidances (e.g., 21 CFR Part 11, ICH/GCP)

·       Knowledge of installation and/or validation of clinical data management system (CDMS) applications in a clinical research environment

·       C#, C++, .NET, Visual Basic or other object-oriented language, and/or SAS programming knowledge / experience not required, but desirable

·       Medidata Rave and iMedNet EDC knowledge / experience not required, but desirable

Reporting application development (e.g., JReview, Business Objects, PowerBI) knowledge / experience not required, but desirable

Education or Equivalent Experience

·       Bachelor’s degree in computer science or other quantitative or scientific discipline with 8+ years’ experience in database programming and demonstrated working knowledge of scientific principles.

·       Commensurate experience with clinical database programming and database administration will be considered as an alternative to a degree

Why SDC

SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances and positive work/life balance, we are able to attract some of the most talented people in the industry.

• We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits.

• We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment.

• We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.

• We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry.

• With a proven track record, SDC has been successfully executing client clinical programs since 2005.

Take a look at how you can join our team!

#LI-Hybrid

Job Summary
We are seeking a dynamic independent and experienced Research Associate in Clinical Management for processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and outside investigators. Ensuring accurate, timely, and consistent data reaches the clinical teams and other groups.
 
Roles & Responsibilities

• You will be responsible to monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), and study protocols under supervision of Clinical Operations Manager/ Clinical Research Specialist.
• You will be responsible to perform study site feasibility, qualification, initiation, monitoring and close-out activities (remotely/ on-site) under supervision in line with study specific project management/ sponsor oversight plan and apply judgment and knowledge to independently resolve site issues, questions, and concerns. 
• You will support Clinical Operations Manager/ Clinical Research Specialist to prepare for project kick-off/ investigator’s meeting.
• You will be desirous to build and maintain relationships with investigators and site staff. 
• You will be responsible to address and resolve issues at sites, including the need for additional training, potential deficiencies in documentation and communication.
• You will responsible for documentations under supervision and ensure maintenance of Trial Master File/ Sponsor Oversight File in line with study specific project management/ sponsor oversight plan. 
• You will Support study sites in making Ethics Committee submissions under supervision in  line with study specific project management/ sponsor oversight plan. 
• You will be responsible to review & follow-up on site payments. 
• You will assist with data query resolution process for site, Clinical Research organisation (CRO) and Sponsors along with Clinical Data Management in line with study specific project 
• management/ sponsor oversight plan.
• You will be responsible to work collaboratively with the study teams with the review, revision and writing of protocols, Case Report Forms (CRF) and other required documents for clinical research studies. 

Computing Educator - College
Location: Shamirpet, Medchal-Malkajgiri district, Telangana
Salary: 06 –10 Lakhs
Basis: Permanent; full-time
Eligibility: You must be eligible to work in India

The role

We are seeking a highly motivated and passionate Computing Educator to join our team at the Coding Academy supported by Telangana Social Welfare Residential Educational Institutions Society in Telangana. The Coding Academy has two strategic academic units: a school located in Moinabad Rangareddy district for grades 6–12, and a college located in Shamirpet, Medchal-Malkajgiri district.

The successful candidate will be responsible for planning and delivering the computing curriculum for learners of the degree college, as well as supporting the Foundation’s work in computing curriculum research and development, teacher training, and related teaching and learning activities.

The role requires a deep understanding of computing subjects, pedagogical principles, excellent communication skills, and the ability to work collaboratively with colleagues.

Key responsibilities:

• Teach the Raspberry Pi Foundation's Computing Curriculum to the learners of the degree college by following the pedagogical principles laid out in the content
• Prepare, conduct, and evaluate internal assessments
• Create and sustain an inspiring, inclusive learning environment in the classroom
• Motivate learners to ask, innovate, experiment and explore, encouraging their curiosity and creativity
• Plan and support learners to ideate and create projects for various state-/national-/global-level events and competitions in related fields
• Observe learners' responses and record them for further actions, providing feedback to learners and working to improve their learning outcomes

• Collaborate closely with the team at the Raspberry Pi Foundation to understand the critical observations made during teaching, test the curriculum, and integrate computing education research and industry trends and topics into lessons

• Collaborate with other fellow educators to bring in more synergy
• Engage with the other teachers at the Coding Academy for effective implementation and support
• Collaborate closely with industry experts and senior computer science educators to organise special sessions, workshops, and industry visits
• Act as a point of contact for state educators on behalf of the Raspberry Pi Foundation, and nurture an educator community

Experience and personal attributes

We recognise that everyone has the potential for growth, and we welcome applications from candidates who can demonstrate that they have some, but not all, of the experience and personal attributes listed here.

• A commitment to the mission and values of the Raspberry Pi Foundation
• Substantial teaching and learning experience, with experience of designing and delivering effective and engaging lesson plans, ideally with a specialism in computing education (Bachelor's degree in Computer Science or a related field and a teaching qualification is highly preferred)
• A proven record of delivering solutions to the formal education system, primarily degree college, and understanding of the relevant/critical success factors
• A demonstrable record of success in areas such as curriculum research and development, monitoring and evaluation, and training of teachers
• A passion for using best-practice pedagogy and research-informed practice in the classroom
• Familiarity with online learning experiences and products, with an understanding of how technology is changing learning is preferable
• Ability to engage with and manage critical school stakeholders during programme implementation work
• Excellent verbal and written communication skills: proficient in reading, writing, and verbal communication in English with a fair level of proficiency in Telugu
• A collaborative, flexible, and solutions-focused approach, with the ability to manage conflicting priorities and complexities
• Good data, analytical, and reporting skills, and the ability to use data effectively to improve what we do
• Willingness to work flexible hours to better cater to the local project requirements
• Comfortable with commuting to the Coding Academy, and owning a vehicle is preferred

About us

The Raspberry Pi Foundation is a UK-based educational charity with the mission to enable young people to realise their full potential through the power of computing and digital technologies.

Established in 2008 and first known for our product — the wildly successful Raspberry Pi computer — the Foundation has developed education programmes, learning experiences, and products that are helping millions of young people learn vital new knowledge and skills.

Tens of thousands of educators have taken our online courses, and millions of people use our free, online learning resources. To deepen our understanding of how young people learn about computing and how to create with digital technologies, we conduct academic research, and we use that knowledge to increase the impact of our work and advance the field of computing education. Through Code Club and CoderDojo, we support the world’s largest network of free, informal computing clubs for young people.

Across all of our work, we are focused on supporting young people who come from backgrounds that are traditionally underrepresented in the field of computing or who experience educational disadvantage. We work all over the world, with teams based in the UK, Ireland, North America, and India, and partnerships with mission-aligned organisations in over 40 countries.

We are at the forefront of the global movement to help young people learn about computing and digital making. You can read more about our mission, values, and goals in our Annual Review 2022 and our Strategy 2022–2025.

Benefits

In addition to competitive salaries, we offer a range of benefits for all of our colleagues, including:

• 15 earned holiday leaves and 16 national holidays
• Life assurance and medical insurance policy
• Highly flexible and balanced work culture to fit around childcare, personal development, and other commitments
• Free subscriptions to well-known programmes in professional development and wellness
• Monthly all-staff meetings and socials

We are currently expecting all interviews to take place remotely online, though with the relaxing of coronavirus measures we may invite candidates for a face-to-face interview if appropriate.

We are committed to safeguarding and promoting the welfare of children and young people, and we expect all staff and volunteers to share this commitment. If successful in the selection process, you will be required to undergo a background check to confirm that you are a suitable person to work with children. Further background checks will be made at regular intervals thereafter.

We are looking for an enthusiastic and organized Staff Research Program Manager to join our Research Operations (Research Ops) team and help support the strategic development of a multidimensional infrastructure that promotes increased efficiency, visibility, and influence of our User Research & Insights Team. This individual will play an integral role in other aspects of Research Ops including organizational and space demands, data knowledge and management, and the development of best practices guidelines.

The Staff Research Program Manager will oversee the planning, coordination, and execution of high-impact customer recruitment projects, research programs, and initiatives within the organization. This role requires close collaboration with internal and external stakeholders to ensure the successful delivery of program objectives, timelines, and deliverables. The Staff Research Program Manager will also manage cross-functional teams, mitigate risks, and drive continuous improvements in customer engagement, research operations, and project execution.

Key Responsibilities:

• Be dedicated to facilitating a great end-to-end experience for customers and partners participating in ServiceNow’s research efforts.
• Help coordinate research activities including identifying and vetting potential customers and partners for research engagements, scheduling study appointments, managing location logistics, generating research materials, assisting with recruiting efforts, and administering participant compensation.
• Communicate with internal and external stakeholders that own customer relationships in all research activities.
• Manage a database of existing and prospective research participants including customer and partner contacts.
• Ensure that our research findings database is always up-to-date and maintained by our researchers, generating reports and progress against the database.
• Identify and document research best practices and tools to increase team efficiency.
• Lead and manage customer recruitment projects and research programs from inception to completion, ensuring alignment with organizational goals and objectives.
• Develop detailed project plans, timelines, and resource allocation to deliver high-quality research outcomes.
• Coordinate and liaise with research teams, external collaborators, and stakeholders, ensuring timely communication and progress updates.
• Provide leadership in program management methodologies and best practices, ensuring consistent and successful delivery of projects.
• Identify and manage potential risks, develop mitigation strategies, and resolve project challenges proactively.
• Facilitate cross-functional collaboration among departments such as sales, product management, and operations.
• Monitor and report on program performance, providing insights and recommendations for continuous improvement.
• Mentor junior Research Program Managers, guiding best practices and professional development.

Job Summary
We are seeking a highly skilled Analytical Scientist to join our Research and Development team. The successful candidate will be responsible for developing, validating, and implementing analytical methods for the quantification and identification of genotoxic impurities in pharmaceutical products. This role will involve extensive use of chromatography techniques and adherence to regulatory standards. The ideal candidate should have a strong background in analytical chemistry, method development, and data analysis, with a keen eye for detail and a commitment to ensuring the highest quality standards.

Roles & Responsibilities

• You will be responsible to review relevant Literature and stay updated with the latest research and scientific literature relevant to the field of genotoxic impurities and chromatography methods.
• You will be responsible to develop and optimize chromatography-based methods for accurately quantifying genotoxic impurities in various samples.
• You will be responsible to address regulatory deficiency queries concerning the analytical methods and data related to genotoxic impurities.
• You will be responsible to ensure the quality and accuracy of reference standards and working standards used in analytical testing and method development.
• You will be responsible to develop analytical methods, conduct validation studies to ensure the accuracy and reliability of the methods, and transfer validated methods to the Quality Control (QC) department.
• You will be responsible to prepare comprehensive reports documenting method development, validation results, and any forced degradation studies performed.
• You will be responsible to conduct forced degradation studies to identify potential impurities and establish their chemical nature and behaviour.
• You will be responsible to perform real-time analysis of samples during product development stages to ensure product quality and consistency.
• You will be responsible for compilation of Stability Data to assess the stability profile of the products under various conditions.
• You will be responsible to evaluate the effectiveness of the product development strategy and identify any cross-functional issues affecting the process.
• You will be responsible to identify and plan for the developmental needs of the product, considering factors such as scale-up and potential process improvements.
• You will be responsible to source and manage the procurement of necessary chemicals, solvents, columns, and other laboratory equipment.
• You will be responsible to ensure proper maintenance of laboratory equipment as per Good Laboratory Practices (GLP) standards to guarantee accurate and reliable results.
• You will be responsible to calibrate instruments as per the calibration schedule and strictly follow Standard Operating Procedures (SOPs) to maintain consistency and accuracy.
• You will be responsible to maintain a clean and organized work area, and ensure that the laboratory environment is controlled at the required temperature for optimal analytical conditions.
• You will be responsible to keep all relevant documents well-maintained and organized for easy access and compliance with internal and external auditing requirements. 

Interactive Response Technologies - Project Manager

Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005.

SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials.

Job Summary

Oversees and coordinates all lRT activities in support of clinical and/or non-clinical research studies for study initiation, setup, maintenance, and closeout. Manages the day-to-day IRT project activities including, but not limited to, timelines, budgets, staff, project scope, reports and communication for the lifecycle of the project(s). Mentors/trains IRT Programmer on IRT build requirements

Primary Responsibilities

·        Lead IRT study setup activities including IRT design and specification (with edit checks) documents and approval and user acceptance testing.

·        Allocate and prioritize workloads for multiple projects

·        Serve as primary client contact for IRT

·        Work with Clinical Data Managers and Statistical Leads with management of timelines and budgets as they pertain to IRT activities

·        Work with study team to reconcile IRT data with clinical data and oversees data transfers

·        Mentor IRT Programmer on IRT build requirements

·        Develop documentation for validation and maintenance of IRT databases for clinical trials using a variety of validated software applications

·        Maintains quality control of the data, project deliverables and closeouts

·        Adhere to all aspects of the SDC's quality system

·        Comply with SDC's data integrity & business ethics requirements

·        Develop and maintain SOPs and tools relating to the IRT

·        Perform other related duties incidental to the work described herein

·        Adherence to all essential systems and processes that are required at SOC to maintain compliance to business and regulatory requirements 

The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.

Required Skills

·        Exceptional working knowledge of clinical trials and IRT role in the clinical trials process

·        A minimum of 1 year of staff mentoring and leadership experience

·        Strong leadership capabilities

·        Strong delegation abilities

·        Highly effective communication skills, both written and verbal

·        Ability to work as a member of a multi-disciplinary team and adapt to changing priorities

·        Training and experience in clinical database management

·        General knowledge of GCPs and the conduct of clinical trials.

·        Understanding of the clinical research process flow and drug development processes.

·        Understanding of software development and testing processes.

·        Demonstrated proficiency in office productivity applications (e.g., Microsoft Word, PowerPoint, and Excel).

·        Excellent organizational skills

·        Ability to manage multiple tasks simultaneously and to prioritize tasks effectively.

·        Demonstrated ability to focus on project work and efficiently bring projects to completion

·        Ability to effectively manage projects, budgets and timelines

·       Ability to learn new systems without formal training

Education or Equivalent Experience

Bachelor's degree in engineering, applied or life science and at least two (2) years of experience in management of an IRT system or an Associate's degree in engineering, applied or life science and a minimum of five (5) years of experience in management of an IRT system.

Why SDC

SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances and positive work/life balance, we are able to attract some of the most talented people in the industry.

• We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits.

• We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment.

• We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.

• We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry.

• With a proven track record, SDC has been successfully executing client clinical programs since 2005.

Take a look at how you can join our team!

#LI-Hybrid

Job Overview

Development of probabilistic flood hazard models for different countries

Roles and Responsibilities

1. Manage the collection and analysis of hydrological data using automation, to integrate the high quality data into the modeling process
2. Develop computer programs to automate data capture and post processing of model results
3. Working with various modules of the flood hazard models.

We're hiring for a Research Analyst position.

Responsibilities:

• Deals with collecting IT, Engineering, Supply chain & Finance jobs and generating required leads of the company.
• Conduct research on Company Profiles of firms belonging to various sectors.
• Use tools like Zoom info, Discover Org tools for generating contacts.
• Conduct research using LinkedIn and other key web-based research tools to find targeted names and profiles. Validate and Manage leads and contacts.
• Database building of B2B contact lists via internet research Data Mining (Extraction & Creation of Relevant Contacts) and Identifying the potential clients.
• Generating Leads for emails Campaigns.
• Ensure email message is conveyed clearly and delivered properly to prospects.
• Ensure messages are sent in proper form and template.

Ideal Candidate:

• 5+ years' experience as a Research Analyst in the US Staffing industry
• Resident of Hyderabad
• Willing to work on-site
• Comfortable commuting to the work location

We're hiring for a Research Analyst position.

Responsibilities:

• Deals with collecting IT, Engineering, Supply chain & Finance jobs and generating required leads of the company.
• Conduct research on Company Profiles of firms belonging to various sectors.
• Use tools like Zoom info, Discover Org tools for generating contacts.
• Conduct research using LinkedIn and other key web-based research tools to find targeted names and profiles. Validate and Manage leads and contacts.
• Database building of B2B contact lists via internet research Data Mining (Extraction & Creation of Relevant Contacts) and Identifying the potential clients.
• Generating Leads for emails Campaigns.
• Ensure email message is conveyed clearly and delivered properly to prospects.
• Ensure messages are sent in proper form and template.

Ideal Candidate:

• 2+ years' experience as a Research Analyst in the US Staffing industry
• Resident of Hyderabad
• Willing to work on-site
• Comfortable commuting to the work location

Job Summary
We are looking for a Lead Data Scientist to manage the strategic delivery of advanced data analytics products, overseeing their development, validation, and maintenance. Your role entails leading a team of data scientists, driving their productivity, and fostering a culture of continuous improvement. By analysing large datasets, optimizing ML frameworks, and collaborating with cross-functional teams, you will ensure the alignment of data science solutions with organizational objectives while maintaining compliance with regulatory requirements.

Roles & Responsibilities
• You will be responsible for delivery of strategic roadmap and plan for advanced data analytics products. This includes developing, validating and maintaining the products.
• You will be responsible for leading the team of data scientists, focusing them on tasks, and driving their productivity and performance.
• You will analyse large volumes of data to identify new patterns using data mining and AI and train and validate models.
• You will be responsible for driving improvement across all governance and performance metrics for the assigned products/projects.
• You will be responsible for developing a cohesive team and fostering a culture of continuous learning and improvement. You will identify training and development opportunities for team members to enhance their skills and capabilities.
• You will be responsible for collaborating with cross-functional teams to understand business needs and identify data science driven solutions.
• Your role includes optimizing existing ML (Machine Learning) frameworks, maintaining up-to-date knowledge of advancements in the field, and tackling challenges with creative analytical solutions.
• You will be responsible for maintaining documentation throughout and beyond the development process including algorithms and technologies related documentation for future reference.
• You will be responsible for maintaining coding and development standards and following procedures to ensure high-quality algorithms and models.
• You will be responsible for ensuring adherence to data governance policies and regulatory requirements surrounding data in the pharmaceutical industry during development and deployment of data analytics products.
• You will be expected to act as a liaison between technical and non-technical stakeholders to ensure alignment of data analytics solutions with organizational goals.

Job Title: Artificial Intelligence/Machine Learning Engineer - R&D

Location: Hyderabad, India (With option for Face-to-Face Interviews in Hyderabad)

Job Summary: Join our innovative team of AI/ML experts in Hyderabad and be a part of shaping the future of Artificial Intelligence! We're seeking a highly skilled and motivated Artificial Intelligence/Machine Learning Engineer with a strong R&D background to design, develop, and deploy cutting-edge AI and ML models that drive business growth and innovation.

Key Responsibilities:

• Design and Develop AI/ML Models: Design, develop, and deploy AI/ML models using various frameworks and technologies such as TensorFlow, PyTorch, Keras, and Scikit-learn to solve complex business problems.
• Conduct R&D and Proof-of-Concepts: Conduct research and development to identify opportunities for AI/ML applications, develop proof-of-concepts, and evaluate their feasibility and potential impact.
• Collaborate with Cross-Functional Teams: Work closely with data scientists, product managers, and engineers to understand business requirements, design AI/ML solutions, and integrate them into our products and services.
• Develop and Deploy AI/ML Pipelines: Develop and deploy AI/ML pipelines using cloud-based platforms such as AWS SageMaker, Google Cloud AI Platform, and Azure Machine Learning to streamline model deployment and maintenance.
• Monitor and Evaluate AI/ML Model Performance: Monitor and evaluate the performance of AI/ML models, identify areas for improvement, and optimize model performance to ensure maximum business value.
• Stay Up-to-Date with Industry Trends: Stay current with the latest developments in AI/ML research and industry trends, and apply this knowledge to drive innovation and improvement in our products and services.
• Mentor and Collaborate with Junior Team Members: Mentor and collaborate with junior team members to share knowledge, provide guidance, and support their growth and development.

Qualifications:

• Master's or Ph.D. in Computer Science, Electrical Engineering, or related field.
• Minimum 5 years of experience in AI/ML engineering with a strong R&D background.
• Strong programming skills in languages such as Python, Java, or C++.
• Experience with AI/ML frameworks and technologies such as TensorFlow, PyTorch, Keras, and Scikit-learn.
• Experience with cloud-based platforms such as AWS SageMaker, Google Cloud AI Platform, and Azure Machine Learning.
• Strong understanding of machine learning algorithms, deep learning, and natural language processing.
• Excellent problem-solving and analytical skills.
• Strong communication and collaboration skills.
• Experience with Agile development methodologies and version control systems such as Git.

Nice to Have:

• Experience with computer vision and natural language processing.
• Experience with reinforcement learning and transfer learning.
• Experience with AI/ML applications in industries such as healthcare, finance, or e-commerce.
• Certifications in AI/ML such as Certified Data Scientist or Certified Machine Learning Engineer.

What We Offer:

• Opportunities for professional growth and development in a collaborative and dynamic work environment.
• Access to cutting-edge technologies and tools to stay ahead of the curve.
• Recognition and rewards for outstanding performance and contributions to the team.
• Five days in office, Monday to Friday, to collaborate with colleagues and drive innovation.
• Face-to-Face Interviews available in Hyderabad for those who prefer in-person interactions.
• Opportunities to work on high-impact projects and contribute to the development of innovative AI/ML solutions.

Job summary
We are looking for an experienced professional with good understanding of molecular biology and mammalian cell culture techniques pertaining to cell line development. The role involves conducting molecular biology & clone development experiments including engineering of the expression vector, preparation of transfection grade DNA transfection, cell line propagation, transfection, cloning and cell expansion, and screening to select high expression clones/banks to develop stable cell lines expressing biotherapeutics.

Roles & Responsibilities
• You will be responsible for actively participating in experiment design, following instructions, and performing experiments. Your key tasks include keeping accurate records, generating and collating data for analysis and discussion, to draw meaningful conclusions from experiments to establish high-expressing stable cell lines effectively, leading to the creation of research cell banks (RCB) for development and campaign studies. 
• Additionally, your role involves executing molecular biology & clone development related techniques with specified quality, maintaining precise records for troubleshooting, participating in data analysis, and preparing presentations for discussions in Cell Line Development department meetings.
• You will design and conduct experiments to determine gene copy number and gene sequencing in cell lines ensuring quality standards for regulatory compliance, recording accurate data, and drafting reports. 
• You will also play a key role in developing methods for master cell banks (MCB) establishment for different product cell lines. This involves participating in experiment design, execution of experiments, recording detailed data, and interacting with development and manufacturing teams for smooth execution.
• You will capture data in approved formats, write technical reports for cell line establishment and genetic stability, prepare Standard Operating Procedures (SOP), and adhere to safety standards.
• Additionally, you will handle laboratory consumables, and contribute to the completion of Installation and Operational Qualification (IOQ) and Performance Qualification (PQ ) for new equipment.