Role Overview: We are looking for motivated Clinical Operations Associates to support the planning, coordination and execution of clinical research activities while ensuring compliance with clinical trial protocols and regulatory guidelines.
Key Responsibilities
- Assist in coordinating clinical trial activities and site operations.
- Maintain clinical trial documentation and records.
- Support informed consent and regulatory documentation processes.
- Ensure compliance with ICH-GCP guidelines and study protocols.
- Coordinate with investigators, research teams and other stakeholders.
- Track study progress and assist with clinical trial reporting. Required
Skills:
- Basic knowledge of Clinical Research and Clinical Trial Operations.
- Understanding of ICH-GCP guidelines and clinical trial protocols.
- Knowledge of TMF/ISF documentation.
- Good communication, coordination and organisational skills.
- Proficiency in MS Office, especially Excel and Word.
- Robust attention to detail and problem-solving abilities. Eligibility: B.
Pharm, Pharm.
D, M.
Pharm, B.
Sc. Life Sciences, Biotechnology, Microbiology, Nursing or other relevant healthcare graduates.