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Clinical Site Manager

Roche
3+ years
preferred by company
Multiple, Locations
1 May 14, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Coaching Skills, Data Science, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Pro, Collaboration, Communication Skills, gmp, GMP Guidelines, Operational Excellence, Problem Solving Skills, Quality Agreements, Quality Compliance, Quality Management, Quality Standards, Regulatory Requ, Communication Skills

Clinical Site Manager

Company: Roche
Category: Research & Development
Job ID: 202605-111620
Employment Type: Full-time
Location: Multiple Locations

Job Overview

The Clinical Site Manager is responsible for planning, coordinating, monitoring, and completing clinical research studies at assigned clinical sites, ensuring compliance with study protocols, GCP, SOPs, and regulatory requirements.

Key Responsibilities

  • Act as primary contact for assigned study sites and clinical trial execution.
  • Train and support site personnel for study conduct and certification.
  • Conduct site qualification, assessment, initiation, monitoring, and closeout visits.
  • Support site activation including contracts, IRB/EC approvals, and regulatory documentation.
  • Develop study site documents such as monitoring plans, informed consent forms, source documents, patient guides, and case report forms.
  • Review study protocols, reports, and data management documentation.
  • Perform end-to-end site monitoring and data validation activities.
  • Collaborate with R&D, Biometrics, Study Management, Field Service, and cross-functional teams.
  • Oversee CRO site management activities and escalate issues when needed.
  • Manage site-level budgets and timelines.
  • Work with investigators, international stakeholders, and key customers.
  • Mentor junior colleagues where required.

Required Skills

  • Clinical site management
  • Clinical trial monitoring
  • GCP (Good Clinical Practice)
  • Regulatory compliance
  • Site activation
  • IRB / EC approvals
  • CRO management
  • Clinical documentation
  • Site qualification visits
  • Study monitoring
  • Data validation
  • Protocol review
  • Budget management
  • Stakeholder management
  • Cross-functional collaboration

Experience

  • 3+ years of experience in regulated clinical research / clinical operations / site management
  • Experience in clinical trial monitoring and site management
  • Experience with GCP, SOPs, and regulatory requirements
  • Experience with CRO oversight preferred

Education

  • Bachelor’s Degree in Scientific Discipline