Clinical Trial Manager

3 days ago

London, United Kingdom MastarRec Full time

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 reportLead cross-functional teams (CRA Data Management Regulatory Biostatistics) and manage CRO oversightDevelop and manage study budgets timelines and site selectionMonitor trial metrics risk mitigation plans and vendor performanceEnsure quality and regulatory compliance with ICH-GCP EMA MHRA and FDA standardsServe as main point of contact for clinical sites investigators and stakeholdersCoordinate and lead internal/external team meetings and status reports.Manage documentation and trial master files (TMF) to inspection-ready standardsRequirementsRequired SkillsExtensive understanding of clinical trial regulations GCP ICH and MHRA requirementsProven experience managing global or multi-site clinical studiesExcellent leadership team coordination and stakeholder management skillsStrong command of trial budget and vendor oversightProficient with EDC systems CTMS and MS Office toolsDesired SkillsLife sciences or health sciences degree (BSc MSc or equivalent)ACRP SOCRA or equivalent clinical research certificationExperience with oncology rare disease or CNS trialsFamiliarity with EU CTR and decentralised trial modelsBenefitsJob BenefitsCompetitive salary with performance-based bonusPrivate medical insurance & pension schemeCareer development pathway with leadership trainingFlexible hybrid working (23 days office-based)Opportunity to manage global multi-centre trialsRequired 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 Key Skills CSS,Cloud Computing,Health Education,Actuary,Building Electrician Employment Type : Full Time Experience: years Vacancy: 1 Yearly Salary Salary: 55000 - 75000

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