Cognizant is hiring for the SPE – Clinical Data Management role in Pune, Maharashtra. The position requires 2–4 years of experience in clinical data management, including data cleaning, discrepancy and query management, database lock activities, and clinical trial data handling. Candidates should have working exposure to Medidata Rave EDC or Veeva EDC, Spotfire reporting, third-party data management, and client communication.
Job Details
| Particulars | Details |
|---|---|
| Company | Cognizant |
| Job Title | SPE – Clinical Data Management |
| Location | Pune, Maharashtra |
| Experience | 2–4 years |
| Employment Type | Full Time, Permanent |
| Qualification | Any Graduate |
| Industry | IT Services & Consulting |
| Department | Data Science & Analytics |
| Job Function | Clinical Data Management |
| Application Source | Naukri |
Positions
Cognizant is recruiting for the SPE – Clinical Data Management position, supporting clinical trials across diverse therapeutic areas.
Responsibilities
- Perform clinical data cleaning, manual checks, and system checks.
- Update relevant trackers and manage discrepancies, queries, and issue resolution.
- Execute database lock activities.
- Coordinate with the Team Lead (TL) to develop action plans for activities that do not meet client service-level agreements (SLAs).
- Archive required documentation and information according to quality and security requirements for audit purposes.
- Support multiple clinical trials across different therapeutic areas.
- Provide technical oversight when required.
- Handle third-party clinical trial data, including laboratory, pharmacokinetic (PK), and imaging data.
- Communicate with clients and support clinical data management activities.
Eligibility and Qualifications
Candidates should meet the following requirements:
- Educational qualification: Any graduate.
- Work experience: 2–4 years.
- Experience in clinical data management activities, including data cleaning, query management, discrepancy resolution, and database lock.
- Working exposure to Medidata Rave EDC or Veeva EDC.
- Knowledge of Spotfire reporting.
- Experience handling third-party clinical trial data.
- Experience in client-facing roles and client communication.
Required Skills
- Clinical Data Management (CDM)
- Medidata Rave EDC
- Veeva EDC
- Spotfire reporting
- Data cleaning and data cleansing
- Manual and system checks
- Discrepancy and query management
- Issue resolution
- Database lock activities
- Third-party data handling
- Clinical trial data management
- Audit documentation and archiving
- Client communication and coordination
- SQL
- Clinical research and clinical trials
1 Execute Data Management Activities I.e., Data Cleaning, Executing Manual and System checks, Update relevant trackers, Discrepancy and query management, Issue resolution, Database lock activities.
2 Identify and develop action plan in coordination with the TL for activities not meeting the client SLAs.
3 Archive all necessary information for audit purposes according to quality and security requirements, to ensure reliable and timely retrieval of documentation and information.
4 Support multiple clinical trials, across diverse therapeutic areas, to successful conclusion and provide technical oversight when required.
5 Working exposure in RAVE/VEEVA EDC, Knowledge of Spotfire reporting tool ,
6 Third party data handling experience (Lab, PK, Image etc), Client facing role (experience in client communication
