inVentiv International Pharma Services Pvt. Ltd
Job Title: Sr CDM I
No. of Posts: 1
- Lead and conduct all DM activities required for global clinical trials.
- Coordinate the work of global staff assigned to the project.
- Provide training on procedures and systems.
- Create project-related materials.
- Track project progress and issue status reports.
- Ensure the achievement of key milestones relating to the function, such as completion of tasks towards final database.
- Attend internal and external meetings.
- May be required to participate in client, internal or agency audits and inspections
- May represent the department at business development related meetings.
1. Lead and conduct all DM activities required for global clinical trials. 1. Lead and conduct all DM activities required for global clinical trials. 2. Should have exp in Query Mgmt & Lab Mgmt, SAE reconciliation, Vendor reconciliation & edit check testing (UAT). 3. Should have min 2.5 yr exp in OC RDC. 4. Good knowledge of DM process and OC RDC CDMS 5. Excellent communication Experience as Lead DM will be an added advantage Education-
UG: Any Graduate – Any Specialization
PG:Any Postgraduate – Any Specialization