Project Coordinator
at WEP Clinical
London W4, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 22 Jul, 2024 | Not Specified | 28 Apr, 2024 | N/A | Good communication skills | No | No |
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Description:
Job Title: Project Coordinator
Department: Project Management
Company: WEP Clinical
Location: Hybrid - Chiswick Tower, London, England
Do you dream of being part of a team that brings hope to those who need it most? Are you searching for a career that challenges you and allows you to grow as a professional? At WEP Clinical, we are expanding, and the opportunities for personal and professional development are endless. Our team is committed to providing patients with early access to life-changing medicine every day. We encourage our team to bring their most creative and innovative ideas. Join us today and discover the incredible impact you can make!
The Project Coordinator for WEP Clinical provides administrative support for Expanded Access Programs (EAP) or Post-Approval Named Patient Programs (PA-NPP).
MORE ABOUT US:
WEP Clinical is a specialist services company that partners with sponsors to help patients and physicians gain early access to medicines when no other treatment options are available. WEP Clinical has over a decade of experience distributing products worldwide to treat unmet patient needs. Our services include Expanded Access Programs (EAPs), Named Patient Programs (NPPs), Clinical Trial Supplies (Comparator & Ancillaries), Wren Nursing (Clinical Trial Home Nursing & Clinical Education) and Hospital Supply of Unlicensed Medicines
Responsibilities:
- Assist Project Management team with administrative tasks associated with EAP or PA-NPP.
- Create and distribute Meeting Agendas and Meeting Minutes for internal and external teleconferences.
- Works with the project management team to ensure projects are completed in accordance with client expectations.
- Assist with project documentation collection and review from investigational sites, ensuring they meet FDA/GCP/ICH requirements.
- Support preparation of study files based on project scope including maintenance of internal or external document storage systems including Electronic Trial Master File (eTMF).
- Enter and maintain program, site, and patient-level data into the Clinical Trial Management System (CTMS).
- Work with the supply chain team to coordinate and dispatch shipments of investigational product according to the WEP Clinical SOP’s.
- Provide support to the Project Management Leadership on various projects.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
A health or science field preferred
Proficient
1
London W4, United Kingdom