Full Time

Assistant Clinical Research

Powered by Monster
Rajasthan
₹ 800000 - ₹1300000 per annum
Posted 14/02/2026

About the Role

Role & Responsibilities
• Assist in the design and implementation of clinical research studies.
• Maintain accurate records of study documentation and patient data.
• Coordinate with clinical trial sites and ensure compliance with protocols.
• Support the preparation and submission of regulatory documents.
• Assist in the collection and analysis of clinical trial data.
• Help train site staff on study protocols and procedures.
• Participate in monitoring visits and audits as required.

Qualification
• Not specified.

Experience
• 0-5 years of experience in clinical research or related fields.

Vacancies
• 1 or more vacancies

Skills
• Data Analysis
• Regulatory Compliance
• Clinical Trials
• Statistical Software
• Patient Recruitment

About The Company
Powered by Monster on behalf of Thepharmadaily, this company specializes in clinical research and recruitment services. They are dedicated to ensuring compliance with regulations and providing accurate and efficient support to clinical trials.

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