Associate Site Manager - Mumbai/bangalore/hyderabad/delhi

Johnson & Johnson

Bangalore, Karnataka, India
Fully remote
On-site clinical trial monitoring
Compliance with gcp and sops
Site initiation and close-out activities
An Associate, Site Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure

Job Summary

  • An Associate, Site Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.
  • The Associate, Site Manager will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and Trial Delivery Leader (TDL) to ensure overall site management while performing trial related activities for assigned protocols.
  • This role involves acting as the primary local company contact for assigned sites, ensuring site staff are trained, managing clinical supplies, and maintaining complete, accurate, and timely data and essential documents.

Matching Summary

An Associate, Site Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.

Skills & Requirements

Must-have

  • On-site clinical trial monitoring
  • Compliance with GCP and SOPs
  • Site initiation and close-out activities
  • Clinical trial protocol adherence
  • Data accuracy and query resolution
  • Adverse event reporting
  • Site recruitment and retention planning

Nice-to-have

  • Process improvement and training
  • Risk-based monitoring implementation
  • Collaboration with cross-functional teams
  • Therapeutic knowledge development
  • Participation in investigator meetings
  • Stakeholder relationship management

Key Requirements

  • 2 - 4 years on-site monitoring experience
  • Bachelor's degree in Life Sciences or related field
  • PhD or MBBS / B.Pharm / M.Pharm is a plus

Work Rights

Not specified

Tailored Resume

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