Project Manager(Clinical Trials)

JSS Medical Research; India; On-site; INR 1,500,000 - 2,600,000; Full time

Job summary

JSS Medical Research in Mumbai is seeking an experienced Clinical Project Manager to oversee trial delivery across investigator sites. The role requires 7–10 years in clinical trials and 2+ years as a project manager, with strong GCP/ICH knowledge.

The position involves site selection, budgeting, regulatory compliance, enrollment strategies, and coordination with sponsors and vendors. Mumbai-based candidates are preferred.

Qualifications

• 7–10 years in Clinical Trials & Clinical Research; must have 2+ years as Project Manager.
• M.Pharma (any specialization) or MS/M.Sc (Science) required.
• Strong understanding of GCP & ICH guidelines.
• Excellent communication for client interaction.
• Must be from Mumbai.

Responsibilities

• Select and assess investigators/sites based on study needs.
• Negotiate budgets, contracts, and sponsor agreements.
• Conduct investigator meetings and site initiation support.
• Develop enrollment strategies and monitor recruitment/retention.
• Oversee study progress for protocol, regulations, and GCP.
• Perform site monitoring and oversee CRA performance.
• Identify and resolve study-specific issues with vendors.
• Ensure timely completion within budgets/resources.
• Track study progress, enrollment, site performance.
• Manage close-out activities, data reconciliation, return of supplies.
• Prepare sites for audits and inspections.
• Ensure compliance with Clinical Trial Material requirements.
• Serve as primary sponsor contact with regular updates.

Skills

GCP & ICH knowledge

Excellent communication

Education

M.Pharma

MS/M.Sc (Science)

Job description

Essential Functions:

• Select and assess clinical investigators/sites based on study requirements.
• Negotiate study budgets, site contracts, and sponsor agreements.
• Conduct investigator meetings and support site initiation.
• Develop enrollment strategies and monitor recruitment/retention.
• Oversee study progress to ensure compliance with protocol, regulations, and Good Clinical Practice (GCP).
• Perform site monitoring visits and oversee APM/CRA performance.
• Identify and resolve study-specific issues and coordinate with vendors.
• Ensure timely study completion within approved budgets and resources.
• Track study progress, enrollment, and site performance.
• Manage study close-out activities, including data reconciliation and return of study supplies.
• Prepare sites for audits and inspections.
• Ensure compliance with Clinical Trial Material requirements, where applicable.
• Serve as the primary sponsor contact and provide regular study updates.
  

Desired Candidate Profile

• 7-10 years of experience in Clinical Trials & Clinical Research industry. MUST HAVE 2+ YEARS EXPERIENCE AS PROJECT MANAGER
  
• M.Pharma (Any Specialization), MS/M.Sc(Science) degree required.
  
• Strong understanding of GCP regulations and ICH guidelines.
  
• Excellent communication skills for effective client interaction.
• Should be from Mumbai.