Site Intelligence Lead
- Company
- Cpl Life Sciences
- Location
- Guildford
- Posted
- 04 Jan 2021
- Closes
- 02 Feb 2021
- Ref
- JO-2011-458293
- Contact
- Sarah Phillips
- Discipline
- Clinical Research, Clinical Research Associate
- Hours
- Full Time
- Contract Type
- Contract
- Experience Level
- Experienced (non-manager)
Study Site feasibility lead
12 month contract
Remote
Offering between 35-47 per hour DOE
Cpl Life Sciences are actively recruiting for a large 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.
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 then please apply or send your up to date CV to sarah.phillips@cpl.com.