Pharmacy, Biotechnology & Life Sciences
Ira Kapoor
Clinical Research Associate
Clinical study coordination and traceable monitoring records.
Professional profile
Clinical Research Associate with an illustrative 11-year career focused on clinical study coordination and traceable monitoring records. Brings together study monitoring, protocol review and source documentation with practical delivery experience. Selected work below shows the problem, my contribution and the handover material rather than unsupported performance claims.
Professional experience
Clinical Research Associate
Asterline Life Sciences
Responsible for scoped clinical study coordination and traceable monitoring records work, coordinating the relevant reviewers and delivery partners.
- Built a protocol-specific review checklist and tracked missing documentation for the responsible team.
- Categorised queries and coordinated responses through the approved study process.
- Maintained traceability and made unresolved questions visible before handover.
Clinical Research Associate
Northmere Life Sciences
Supported progressively more complex work in clinical study coordination and traceable monitoring records, with a defined review process.
- Used study monitoring and query management on assigned work; recorded decisions so colleagues could understand the approach.
- Prepared query tracker and follow-up record and incorporated specialist feedback before closing the workstream.
Research / Practice Associate
Cedarfield Life Sciences
Built foundations through supported assignments, observation and practical feedback.
- Assisted with protocol review and site coordination, checking work with an experienced reviewer.
- Kept organised work records and developed clear handover habits through supervised practice.