Clinical Project Manager

I am working with a fantastic fast-growing CRO who are actively seeking to hire a Clinical Project Manager to join their Clinical Operations team on a permanent basis. This is a great opportunity to work with a variety of big pharma & biotech businesses on a range of therapeutic areas. This could be an excellent role for a Lead CRA or an experienced Clinical Project Manager who has come from a clinical background with a strong emphasis on on-site management.

Key Responsibilities include:

• Working with the Clinical Operations study team, responsible for clinical operational oversight and execution of all assigned studies.
• Contribute to operational aspects of the design, content, and preparation of clinical protocols, amendments, consent forms, study guides, monitoring plans, CRFs, and subject information sheets
• Monitoring of study deliverables
• Performing protocol-related site management activities
• Participating in study planning and set-up activities including vendor management, project management, and coordination of the study and implementation plans
• Supporting vendor relationships
• Using relevant reports, identify the progress of CRF data collection and query resolution

Ideal Background:

• Bachelor of Science Degree in Life sciences or Nursing background or equivalent
• 3+ years’ experience in the pharmaceutical or biotech industry, ideally with experience gained at a CRO, working in the management of clinical trials
• Proven experience working in a range of therapy areas
• A team player with the flexibility to work over multiple projects if required
• Excellent communication skills (written and oral)
• Able to proficiently represent the Clinical Operations Dept and the overall business across all functions as well as external parties and KOLs