Roles & Responsibilities:
• Conduct clinical trials in compliance with ICH-GCP and protocol guidelines
• Support study start-up activities and assist with site initiation
• Participate in recruitment and retention of study subjects
• Complete and maintain source documents, CRFs, and logs accurately
• Compile and update the Site Master File
• Manage Investigational Products (IP), including accountability and shipping
• Coordinate submissions and communication with the Ethics Committee
• Update sponsors on study progress and prepare for monitoring visits
• Perform other responsibilities assigned by management
Qualifications:
• Graduates/postgraduates in Life Sciences, Pharmacy, Biotechnology, or related fields
• Freshers with a completed Clinical Research course can also apply
Experience:
• 2–4 years in clinical research or relevant field (freshers with certification considered)
Skills:
• Strong interest in clinical trials and regulatory compliance
• Excellent organizational, communication, and documentation skills
About the Organization:
This organization is dedicated to conducting high-quality clinical trials with a focus on regulatory compliance and data integrity. They provide a collaborative environment where professionals can grow their careers in clinical research and contribute to innovative healthcare solutions.
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