
Senior Clinical Data Standards Consultant
2 weeks ago
ICON plc continues to drive efficiencies through the standardization of data management practices. This role supports the creation and maintenance of content in the Data Standards Catalog under guided supervision. The individual will collaborate with representatives from various functions and leverage industry standards to develop clinical data collection instruments and their associated checks.
Responsibilities- Update metadata definitions and specifications in line with CDISC Study Data Tabulation Model (SDTM/CDASH) and controlled terminology.
- Participate in relevant governance team meetings and provide input on standards as assigned.
- Collaborate with Senior/Principal Data Standards Specialists or Managers to implement data standards strategy, ensuring compliance with regulations and internal governance procedures.
- May act as a subject matter expert (SME) for specific topics.
- Provide ongoing support to the Data Management organization and key stakeholders (e.g., Clinical, Biostatistics, Medical, Medical Writing, etc.).
- Contribute to Data Management or cross-functional initiatives as needed.
- May oversee and hold accountable CRO/FSP data managers and/or database development teams.
Attend and represent the Data Standards team in the following forums, including but not limited to:
Data Standards Governance meetings
- Clinical study team meetings
- Project update meetings
You are:
- Demonstrates a foundational knowledge of Data Management and Data Standards processes, along with awareness of industry best practices.
- Basic understanding of applicable regulations including 21 CFR Part 11, ICH-GCP Guidelines, and CDISC standards for data collection.
- CDISC standards, SCDM certification, or Medidata RAVE certification is a plus.
- Minimum of 2 years of clinical data standards experience in biotechnology, pharmaceutical, or health related
industry is required. - Education: Requires BS in a Science, Health or Computing, or related field
What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family's needs
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON:
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
-
Clinical Quality Assurance Compliance
7 days ago
Bengaluru, Karnataka, India Maxis Clinical Sciences Full timeJob Title: Clinical Quality Assurance Compliance & trainingExperience: 5 plus yearsLocation: MumbaiType: Full-timeExperience Level: [Senior] Manager/Senior ManagerDepartment: Clinical Research Department Purpose of this Role:This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be...
-
Senior Clinical Data Manager
1 week ago
Bengaluru, Karnataka, India beBeeDataManagement Full time ₹ 10,00,000 - ₹ 15,00,000Job Title: Senior Clinical Data AssociateJob Description:Our organization seeks a highly skilled Senior Clinical Data Associate to play a vital role in the clinical trial data management process. This position involves providing support and assistance in all aspects of data management, from study start-up to post-database lock for assigned projects.Main...
-
Senior Clinical Data Analyst
1 week ago
Bengaluru, Karnataka, India beBeeClinical Full time ₹ 1,50,00,000 - ₹ 2,00,00,000Key Roles of Senior Clinical MonitorThe Senior Clinical Monitor plays a crucial role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.As a senior-level professional, you will lead development of robust Quality Management Plans (QMPs) by collaborating...
-
Senior Clinical Data Manager
2 weeks ago
Bengaluru, Karnataka, India Elucidata Full time US$ 1,50,000 - US$ 2,00,000 per yearJob Title: Senior Scientific Manager, ClinicalFunction:R&DLocation:Delhi/Bangalore (Hybrid)About the Company:Elucidata is a TechBio Company headquartered in San Francisco. Our mission is to make life sciences data AI-ready. Elucidata's LLM-powered platform Polly, helps research teams wrangle, store, manage and analyze large volumes of biomedical data. We are...
-
Clinical Research Associate
2 weeks ago
Bengaluru, Karnataka, India MS CLINICAL RESEARCH Full time ₹ 9,00,000 - ₹ 12,00,000 per yearJob Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical...
-
Senior Clinical Data Specialist
3 days ago
Bengaluru, Karnataka, India beBeeClinicalData Full time ₹ 12,00,000 - ₹ 20,00,000Job Title: Senior Clinical Data SpecialistThe Senior Clinical Data Specialist plays a vital role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management. This position involves leading the development of Risk-Based Quality Management (RBQM) plans,...
-
Clinical Data Specialist
4 days ago
Bengaluru, Karnataka, India beBeeData Full time ₹ 12,00,000 - ₹ 16,00,000Job SummaryThe Senior Clinical Data Associate plays a vital role in supporting the clinical trial data management process from start-up to post-database lock for assigned projects under direct supervision.Key responsibilities include:Providing backup support to Lead DM and working as part of a team, ensuring continuity and timely task completion.Performing...
-
Senior clinical data associate
2 weeks ago
Bengaluru, Karnataka, India Precision For Medicine Full timePosition SummaryThe Senior Clinical Data Associate provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and...
-
Senior Clinical Data Specialist
1 week ago
Bengaluru, Karnataka, India beBeeMedical Full time ₹ 1,20,00,000 - ₹ 1,50,00,000Job Overview">The Centralized Monitoring Unit is a department within Clinical Drug Development that brings together skilled medical professionals and technical programmers to ensure patient safety and wellbeing of all clinical trial participants.">As a Senior Medical Reviewer, you will be responsible for conducting comprehensive medical reviews of clinical...
-
Senior Clinical Data Associate
2 weeks ago
Bengaluru, Karnataka, India Precision For Medicine Full timePosition SummaryThe Senior Clinical Data Associate provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and...