Clinical Trial Specialist

Advanced Clinical is hiring a Clinical Trial Specialist to join a growing oncology-focused European pharmaceutical company through our Functional Service Provider (FSP) model. This is a fully remote, home-based role open to candidates based in the UK.

As part of the Clinical Operations team, you'll support the Clinical Trial Manager across Phase I-IV studies, helping deliver trials in line with GCP and SOPs from start-up through to close-out.

• Supporting study and site feasibility, start-up, maintenance and close-out activities
• Managing essential documents and overseeing the Trial Master File (TMF)
• Helping prepare and maintain study documents, including ICFs, study manuals and site materials
• Tracking study progress, enrolment, deviations and site performance
• Reviewing monitoring visit reports and supporting site oversight, with the opportunity to carry out co-monitoring or oversight visits
• Supporting CRO and vendor oversight, including deliverables and invoice review
• Organising study meetings, taking minutes and maintaining risk, issue and decision logs
• Contributing to data review, query resolution and safety reviews

• At least 2 years clinical research experience (3+ preferred), ideally within pharma
• Background as a CRA, site monitor, or study coordinator is a strong advantage
• Solid working knowledge of GCP and an understanding of the clinical development phases
• Experience with eTMF and CTMS systems (e.g., Veeva Vault, Smartsheet, SharePoint)
• Strong MS Office skills and excellent written and verbal communication
• Able to work independently and as part of a team
• BA/BS, nursing degree, or equivalent, ideally in a science subject

• Location:
  
  Remote, UK only
• Travel: 10-20%
• Engagement: FSP, dedicated to a single sponsor