- Perform data reconciliation activities.
- Enter and manage Data Clarification Requests (DCRs).
- Perform Quality Control (QC) of DCRs.
- Update and maintain reconciliation spreadsheets.
- Ensure data accuracy, completeness, and timely resolution of discrepancies.
- Collaborate with cross-functional teams to support high-quality clinical trial data.
Preferred Qualifications:
- Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, or a related field.
- 2+ years of relevant experience in clinical research or clinical data coordination.
- Experience with data reconciliation, DCRs, and quality review activities.
- Hands-on experience with EDC systems such as Medidata Rave, Veeva, Oracle Clinical, Inform, or similar platforms.
- Good understanding of ICH-GCP guidelines and clinical trial processes.
- Solid analytical, documentation, and communication skills.