Summary:
Involved in planning, conducting, and monitoring clinical trials to ensure compliance and data integrity.

Roles & Responsibilities:

• Assist in protocol development and trial documentation.

• Monitor clinical trial sites and ensure regulatory compliance.

• Collect and analyze clinical data.

• Coordinate with CROs, investigators, and ethics committees.

Qualifications:

• B. Pharm or M. Pharm with specialization in clinical research preferred.

Skills:

• Knowledge of GCP, ICH guidelines, and regulatory norms.

• Analytical thinking and attention to detail.

• Strong documentation and reporting skills.