Job Title : Clinical Regulatory Specialist

Job Summary:
Ensures compliance of clinical trial documentation with regulatory standards.

Roles and Responsibilities:

Prepare and review clinical trial documents.
Manage ethics committee submissions.
Support clinical study monitoring.
Liaise with investigators and sponsors.

Qualifications Needed:

Bachelor’s degree in life sciences or clinical research.
Experience in clinical trial management preferred.

Skills Required:

Knowledge of clinical trial regulations.
Strong organizational skills.
Effective communication.

Benefits-

Competitive salary
Annual appraisal and bonuses
Rewards and Recognition
Performance based bonuses

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