Clinical Trial Manager
- Hiring from
- United Kingdom
- Work type
- Hybrid
- Posted
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About Us
MastarRec is a specialist recruitment and staffing agency supporting high-growth and technology-driven industries across the United Kingdom, the United States, and global markets. We partner with organizations to deliver tailored staffing solutions focused on quality, integrity, and long-term value for both clients and candidates.
Job Description
We are hiring a highly experienced and proactive Clinical
Trial Manager (CTM) to lead and manage full-cycle clinical trial
operations. In this role, you will oversee the planning, initiation, execution,
and closeout of Phase I–IV trials across therapeutic areas, ensuring compliance
with ICH-GCP, MHRA, and sponsor guidelines.
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.
- 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
