Clinical Data Specialist
📍 Location: Kochi, India (Hybrid)
📄 Requisition ID: R1483495
🕒 Job Type: Full-time
🌐 Additional Locations: Bengaluru, India | India
About the Role
The Clinical Data Specialist will play a key role in ensuring the accuracy, integrity, and completeness of clinical trial data. This position requires excellent attention to detail, strong organizational skills, and the ability to work independently in a fast-paced, collaborative environment.
Key Responsibilities
Perform clinical data review and validation to ensure data accuracy and consistency.
Apply medical terminology knowledge to verify and interpret clinical data.
Maintain data integrity across all study phases in compliance with regulatory and SOP requirements.
Communicate effectively with cross-functional teams, including Data Management, Clinical Operations, and Project Management.
Identify, investigate, and resolve data discrepancies using established procedures and judgment.
Document all data management activities in accordance with Good Clinical Practice (GCP) and company standards.
Contribute to process improvement initiatives to enhance data quality and efficiency.
Maintain positive, productive relationships with coworkers, managers, and clients across global locations.
Qualifications
Required:
Bachelor’s degree in Clinical, Biological, or Mathematical Sciences (or a related field).
Equivalent combination of education, training, and experience may be accepted in lieu of degree.
Exposure to medical terminology and a solid understanding of clinical research processes.
Excellent organizational, communication, leadership, and computer skills.
Strong attention to detail and ability to manage multiple priorities effectively.
Ability to act independently and take initiative in resolving problems.
Proven ability to build and maintain effective working relationships with internal teams and external stakeholders.
Preferred Skills (Good to Have):
Prior experience in Clinical Data Management (CDM) or clinical research environment.
Familiarity with CDMS tools (e.g., RAVE, InForm, OCRDC).
Basic understanding of clinical trial lifecycle and regulatory guidelines.
About IQVIA
IQVIA is a global leader in clinical research, healthcare analytics, and life sciences consulting. By combining advanced technology with deep scientific expertise, IQVIA accelerates the development of innovative treatments that improve patient outcomes and global health.
🌐 Learn more at https://jobs.iqvia.com
How to Apply
🔗 Apply Now: IQVIA Careers – Clinical Data Specialist
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