Clinical Trial Manager

You’ll serve as a strategic point of contact for internal
teams, CROs, clinical sites, and vendors — delivering high -quality clinical
trials on time and within budget. This is an excellent opportunity for a
professional looking to advance their leadership career in clinical research
management.

Job Responsibilities

• Oversee
  clinical trial planning and implementation from protocol development
  through final study report
  
• Lead
  cross -functional teams (CRA, Data Management, Regulatory, Biostatistics)
  and manage CRO oversight
  
• Develop
  and manage study budgets, timelines, and site selection
  
• Monitor
  trial metrics, risk mitigation plans, and vendor performance
  
• Ensure
  quality and regulatory compliance with ICH -GCP, EMA, MHRA,
  and FDA standards
  
• Serve
  as main point of contact for clinical sites, investigators, and
  stakeholders
  
• Coordinate
  and lead internal/external team meetings and status reports.
  
• Manage
  documentation and trial master files (TMF) to inspection -ready standards
  

Requirements

Required Skills

• Extensive
  understanding of clinical trial regulations, GCP, ICH, and MHRA requirements
  
• Proven
  experience managing global or multi -site clinical studies
  
• Excellent
  leadership, team coordination, and stakeholder management skills
  
• Strong
  command of trial budget and vendor oversight
  
• Proficient
  with EDC systems, CTMS, and MS Office tools
  

Desired Skills

• Life
  sciences or health sciences degree (BSc, MSc, or equivalent)
  
• ACRP,
  SOCRA, or equivalent clinical research certification
  
• Experience
  with oncology, rare disease, or CNS trials
  
• Familiarity
  with EU CTR and decentralised trial models
  

Benefits

Job Benefits

• Competitive
  salary with performance -based bonus
  
• Private
  medical insurance & pension scheme
  
• Career
  development pathway with leadership training
  
• Flexible
  hybrid working (2–3 days office -based)
  
• Opportunity
  to manage global, multi -centre trials