About the Role
We are looking for a Senior Clinical Data Coordinator to join our growing team. This role offers the opportunity to work on a variety of clinical studies while collaborating with cross-functional teams, CROs, and stakeholders to ensure high-quality data management throughout the study lifecycle.

Key Responsibilities

- Lead and manage clinical data management activities under the guidance of a Programme Data Manager.
- Coordinate non-R&D; studies, with some exposure to medical studies.
- Build strong working relationships with CROs and internal stakeholders.
- Review study protocols and provide data management recommendations.
- Support the Programme Manager and collaborate with S&P; teams.
- Apply strong clinical data management principles to ensure high-quality study delivery.

Essential Requirements

- 3-4 years of Clinical Data Management experience.




- Experience leading clinical studies under the supervision of a Programme Data Manager.
- Experience with non-R&D; studies and exposure to medical studies.
- Minimum 3 years of CDISC experience.
- Strong communication, stakeholder management, and problem-solving skills.

Nice to Have

- Experience in Non-Interventional Studies (NIS).
- Medical Affairs experience.
- Real World Evidence (RWE) experience.

If you don't have direct Non-Interventional, Medical Affairs, or RWE experience, we'd still like to hear from you if you can demonstrate robust Clinical Data Management expertise and experience supporting complex or non-standard study designs.

📌 Senior Clinical Data Coordinator (Bengaluru)
🏢 PHASTAR
📍 Bengaluru