Clinical Trial Manager
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Yearly Salary:
Experience Required:
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
We are hiring a highly experienced and proactive Clinical Trial Manager (CTM) to lead and manage full-cycle clinical trial this role you will oversee the planning initiation execution and closeout of Phase IIV trials across therapeutic areas ensuring compliance with ICH-GCP MHRA and sponsor guidelines.
Youll 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 (23 days office-based)
- Opportunity to manage global multi-centre trials
Required Skills:
Required Skills Strong proficiency in CRISPR/Cas9 genome editing Molecular cloning PCR gel electrophoresis and sequencing Experience working with mammalian and bacterial cell lines Familiarity with LIMS and laboratory data management tools Excellent documentation and scientific communication skills Desired Skills PhD or MSc in Genetics Molecular Biology or Biomedical Engineering Experience in bioinformatics tools (e.g. BLAST Geneious Benchling) Knowledge of synthetic biology or mRNA therapeutics Published peer-reviewed scientific research in the field
Company Industry
IT Services and IT Consulting
Key Skills
- CSS
- Cloud Computing
- Health Education
- Actuary
- Building Electrician
