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.

- Positive communication, coordination and organisational skills.

- Proficiency in MS Office, especially Excel and Word.

- Strong 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.

📌 Clinical Operations Associate (Bengaluru)
🏢 Airvin Skills
📍 Bengaluru