PE Global is currently recruiting for a Clinical Trial Manager for an initial 12-month contract role with a leading multinational Biopharma client based in London.
This role will be supporting a Rare Disease programme and will be responsible for the day-to-day management of studies.
Job Responsibilities
- Overall study execution oversight
- Study protocol and Informed Consent Form (ICF) development
- Study resource planning
- Study timelines
- Vendor oversight
- Study start-up – site selection and activation
- Drug / Investigational Product (IP)
- Study quality
- Study budget oversight
- Recruitment, enrolment, and monitoring
- Study outcome and data deliverables
- Study closeout
- Insurance
- Lead or participate in study -specific projects that have a wider program impact; Collaborate with study managers/cross-functional team members to implement
Requirements
- Minimum of 2yrs+ global study management experience in complex therapeutic areas which includes vendor management
- Gene therapy & rare disease experience preferred but not essential
- Medidata RAVE, IxRS, eTMF (Veeva Vault).
Interested candidates should submit an updated CV.
Please click the link below to apply, call Veronica on +44 203 868 9000 or alternatively send an up to date CV to veronica.perez@peglobal.net
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***
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