Clinical Data Management Associate
ClinoGenesis Research Institute
Pune City, Maharashtra, India0–2 yrs3d agovia LinkedIn
About the Role
ClinoGenesis is seeking motivated, detail-oriented Clinical Data Management (CDM) Associates to join our team. This role offers the opportunity to gain hands-on experience in the clinical research industry, working on live clinical trial projects and top industry EDC platforms. You will learn directly from experienced professionals and play a crucial role in ensuring data accuracy for life-changing clinical trials.
Key Responsibilities
As a CDM Associate, you will support the data lifecycle from study start-up to database lock:
- Review eCRFs/CRFs for accuracy, completeness, and consistency to identify and resolve discrepancies.
- Assist with Electronic Data Capture (EDC) systems, database testing, and query management with clinical trial sites.
- Perform quality checks and reconcile clinical data with lab and safety data sources.
- Follow Good Clinical Practice (GCP), CDISC standards, and standard operating procedures (SOPs).
- Work alongside Clinical Operations, Medical Coding, Pharmacovigilance, and Biostatistics teams.
Requirements & Tech Stack
- Experience Level: Fresher (0–2 Years)
- Location: Remote
- Education: B.Pharm / M.Pharm, B.Sc / M.Sc (Life Sciences, Biotechnology, Biochemistry, Microbiology, Clinical Research, or related fields).
- Understanding of Good Clinical Practice (GCP) and basic CDM concepts.
- Strong analytical thinking, attention to detail, and problem-solving skills.
- Excellent written and verbal communication skills.
- Proficiency in basic MS Excel and computer operations.