12 month contract
Fully remote working
Offering between £35-47 per hour DOE
Cpl Life Sciences are actively recruiting for a leading global pharmaceutical company to join their Study Start-up team. This position will perform multiple tasks to assist with the feasibility and improve operational activities, specialist in site fesability activities.
The main responsibilities for this position shall include:
- Support the process relating to global site feasibility activities
- Act as a primary contract for the study team
- Maintain documentation for the feasibility lead from early estimate, feasibility, assumptions and site selection
- Clear implementation plans and performance metrics agreeing timelines and quality
- Liaise with stakeholders both internally and externally
- Streamline appropriate processes for maximum productivity
Key experience and qualifications:
- Site feasibility experience is a must, ideally with global experience
- Previous experience working with CRO's
- Knowledge of the clinical research process and regulatory requirements
- Proficient in Microsoft Office Suite
- Ability to multitask and work to tight deadlines
- Strong presentation and interpersonal skills
- Ideally experience within Vaccines
If this role is of interest to you or you would like more information on the role then please apply or send your up to date CV to sarah.phillips@cpl.com.
