At a Glance
- Tasks: Lead and manage full-cycle clinical trial operations across various therapeutic areas.
- Company: MastarRec, a specialist recruitment agency in high-growth industries.
- Benefits: Competitive salary, private medical insurance, pension scheme, and flexible hybrid working.
- Other info: Opportunity to manage global, multi-centre trials with career development pathways.
- Why this job: Advance your leadership career while making a real impact in clinical research.
- Qualifications: Extensive knowledge of clinical trial regulations and proven management experience.
The predicted salary is between 55000 - 75000 £ per year.
- London, United Kingdom | Posted on 27/11/2025
- Salary £55,000 - £75,000 / year (depending on experience)
- City London
- Province City of London
- Country United Kingdom
- Postal Code EC2A
About Us
Mastar Rec 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 trialoperations.
In this role, you will oversee the planning, initiation, execution, and closeout of Phase I-IV trials across therapeutic areas, ensuring compliancewith
ICH-GCP ,
MHRA , and sponsor guidelines.
You’ll serve as a strategic point of contact for internalteams, CROs, clinical sites, and vendors — delivering high-quality clinicaltrials on time and within budget.
This is an excellent opportunity for aprofessional looking to advance their leadership career in clinical researchmanagement .
- Overseeclinical trial planning and implementation from protocol developmentthrough final study report
- Leadcross-functional teams (CRA, Data Management, Regulatory, Biostatistics)and manage CRO oversight
- Developand manage study budgets, timelines, and site selection
- Monitortrial metrics, risk mitigation plans, and vendor performance
- Ensurequality and regulatory compliance with
- ICH-GCP ,
- EMA ,
- MHRA , and FDA standards
- Serveas main point of contact for clinical sites, investigators, andstakeholders
- Coordinateand lead internal/external team meetings and status reports.
- Managedocumentation and trial master files (TMF) to inspection-ready standards
Requirements
- Required Skills
- Extensiveunderstanding of clinical trial regulations,
- GCP ,
- ICH , and
- MHRA requirements
- Provenexperience managing global or multi-site clinical studies
- Excellentleadership, team coordination, and stakeholder management skills
- Strongcommand of trial budget and vendor oversight
- Proficientwith EDC systems, CTMS, and MS Office tools
- Desired Skills
- Lifesciences or health sciences degree (BSc, MSc, or equivalent)
- ACRP, SOCRA, or equivalent clinical research certification
- Experiencewith oncology, rare disease, or CNS trials
- Familiaritywith EU CTR and decentralised trial models
- Competitivesalary with performance-based bonus
- Privatemedical insurance & pension scheme
- Careerdevelopment pathway with leadership training
- Flexiblehybrid working (2-3 days office-based)
- Opportunityto manage global, multi-centre trials
- #J-18808-Ljbffr
Clinical Trial Manager employer: MastarRec
Join a leading biotechnology firm that prioritises innovation and compliance in the healthcare sector. With a competitive salary, hybrid working options, and a commitment to professional development, this company fosters an inclusive culture that encourages employee growth and collaboration. As a Regulatory Analyst, you'll play a vital role in shaping product development while enjoying a supportive environment that values your expertise and contributions.
