This Senior Clinical Data Management (CDM) position is a specialized opportunity for experienced professionals to lead end-to-end data lifecycles within a hybrid work model across India. Requiring a minimum of 7 years of expertise, the role focuses on the strategic oversight of study and compound portfolios, ranging from initial protocol review and CRF design to final database lock. A mandatory requirement for this role is proficiency in Veeva EDC, as the lead will be responsible for implementing data management plans and overseeing vendor deliveries to ensure strict adherence to SOPs. For Life Sciences or Pharmacy graduates, this role offers a high-impact career path in clinical research and data integrity within a dynamic, tech-forward environment.
About the job
Skill – Clinical data management , Veeva EDC(Mandatory)
Experience – 7+
Location – PAN India(Hybrid)
Notice period : Immediate to 30 days
• 7+years of experience in managing end-to-end Clinical Data Management tasks. ( include study , compound portfolio lead experience)
•Experience in all aspects of clinical data management from protocol review, CRF design to database lock within expectations as per organization defined Standard operating procedures
• Experience in effective development & implementation of clinical data review/management plans/documents and document preparation
• Experience in setup and overseeing Clinical Data Management vendors, responsible for data review and delivery
• Must have Veeva EDC experience to lead projects for end to end CDM task
• Bachelor’s Degree required. Life sciences, Pharmacy or relevant fields preferred.
