Clinical Study Coordinator - London, United Kingdom - Allen Recruitment Consulting

Allen Recruitment Consulting

Verified Company

London, United Kingdom

3 weeks ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Location:

London, Greater London, United Kingdom
Type:
Contract
-
Job #24625

Based in the heart of London, our client is a global pharmaceutical company focused on developing first class therapeutics.

They require a
Clinical Study Codinat with 3+ years of experience to join them on a 12-month contract to contribute to lead tasks related to the oversight of site moniting, vend management, and other activities as delegated by the Study Manager Program Lead.

This may include contributing to and/ suppting study related matters that impact study participant safety, data integrity, study timelines, quality, and budget.

Location:

London/Hybrid (3 days a week remote/2 day onsite)

Contract Type:
(Inside IR35)

BBBH: 24625

Responsibilities:

Develop study specific documentation, as delegated by the Study Manager
Contribute to the oversight of country and site feasibility assessment and site selection. Oversight of CRO f
IRB/EC related submission/approval activities Oversight of essential documents f

-study life-cycle management Develop/Oversee site and investigat
-training materials Present at investigat
-meetings as assigned

Ensure accurate and timely study entry and updates to Facilitate Screening Authization F

- ms sign off and oversee tracking, where applicable Process documents f
-signature in DocuSign

Oversight of Clinical Trial Insurance Attend Global Study Operations team, vend, and/
Cross-Function Study Execution Meeting(s) as GSO representative and take meeting minutes as requested.
Oversee and manage essential documents in the Trial Master File (TMF)
Contribute to Global Study Operations risks identification and mitigations. Provide supp

- t and administrative assistance with internal and external meetings

Requirements:

3+ years of relevant experience

A degree in nursing, life
- health sciences is preferred. Relevant industry experience in lieu of education may be considered. Demonstrated experience in overseeing external vends such as CROs, central labs, and imaging vend
- s.

Proficient knowledge of study management and execution, compliance and quality, drug development and study design, and product and therapeutic area knowledge.
Experience in developing studyspecific documentation and overseeing country and site feasibility assessment and site selection. Ability to oversee CRO f
IRB/EC related submission/approval activities.

Experience in facilitating Screening Authization F
- ms sign off and overseeing tracking where applicable

Still interested in this opptunity?
Submit your CV (in a Microsoft Wd fmat) today