Clinical Research Coordinator

Roles & Responsibilities
• Prepare, review, and submit Ethics Committee (EC) applications and related regulatory documents
• Coordinate with Principal Investigators and site teams at AIIMS Bhubaneswar for EC submissions
• Maintain and regularly update EC submission trackers and documentation logs
• Ensure compliance with ICH-GCP guidelines, Indian regulatory requirements, and internal SOPs
• Support EC amendments, continuing reviews, annual reports, and EC correspondence
• Assist in overall clinical trial documentation and record management at the site

Qualification
• B.Pharm, M.Pharm, Pharm.D, M.Sc / B.Sc / Life Sciences

Experience
• 1-2 years of experience as a Clinical Research Coordinator or in a similar clinical research role
• Mandatory hands-on experience in Ethics Committee (EC) submissions

Skills
• Strong knowledge of GCP and regulatory documentation
• Good understanding of clinical trial processes and site operations
• Excellent communication and coordination skills
• Strong organizational abilities and attention to detail
• Ability to manage multiple submissions and timelines effectively

About the Company
Accede Clinicals is a growing clinical research services organization providing support across clinical trial operations, regulatory coordination, and site management, offering professionals valuable exposure to structured clinical research environments at reputed institutions like AIIMS.