I have an exciting opportunity to join the expanding Late Phase Clinical Operations team as a Clinical Trial Manager Associate

Role:

• Must meet all requirements for Clinical Trial Management Associate position and have demonstrated proficiency in all relevant areas.
• Manage European Country components of Phase 2 or 3 trials as a member of the study team
• Coordinates CROs or vendors as required and demonstrates an ability to work independently
• Provides assistance in site selection, study implementation and ongoing coordination of study sites, either directly or via CROs.
• Assist global trial managers with set-up of central labs and study vendors as required, including liaising with study management CRO to ensure site training and timely initiation
• Review of trip reports generated by CRO CRAs
• Assist in the training of Clinical Trial Management Associates and Clinical Project Assistants

Knowledge, Experience and Skills

• BSc or BA in a relevant scientific discipline or RN qualification
• Relevant clinical trial experience in the pharmaceutical or health care industry or equivalent
• CRA experience preferred
• Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable.
  

Parkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.