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Clinical Trial Leader - Phase I Oncology - FSP - Remote, Uxbridge
Client:
Location: Uxbridge, United Kingdom
Job Category: Job training programs Other
EU work permit required: Yes
Job Reference: Job training programs 2e97aebe9d52
Job Views: 7
Posted: 13.02.2025
Expiry Date: 30.03.2025
Job Description:
Job Title: Clinical Trial Leader - Phase I Oncology - FSP - Remote
Job Location: Uxbridge, UK
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level: Mid-Senior level
Parexel is currently recruiting for an experienced global trial manager/project manager, who has experience within Phase I Oncology trials.
In this position, you will be an invaluable and key member of the clinical delivery team, accountable for the set-up, execution, and delivery of your assigned trials, contributing to the delivery of the sponsors' pipeline through accurate planning and efficient execution of trials that bring speed and value to participating subjects and sites.
Some Specifics About This Advertised Role:
* Accountable for the accurate planning and operational feasibility of trial timelines; and oversight of trial preparation to ensure trial team members are aligned and on track. Supports development of trial level documents owned by other functions.
* Verifies and provides input into the country allocation and oversees trial feasibility.
* Accountable for development and implementation of trial level engagement plans, recruitment planning, and risk mitigation. Leads development of core trial and patient-facing documents. Integrates patient site level feedback during document development and ensures trials are designed with a focus on patient value.
* Maintains oversight during clinical trial conduct including adherence to GCP and all global and local regulatory requirements; compliance with SOPs and continuous risk monitoring/mitigation. In collaboration with other functions, ensures budget oversight, including support of regular clinical quality monitoring, SMC/DMC management, and safety reporting.
* Prepare and implement amendments of core documents, including training material updates/retraining as needed.
* In collaboration with other functions, ensures timely cleaning and delivery of clinical trial data. Coordinates and supports trial medical writer in providing the CTR.
* Responsible for timely, complete, and compliant archiving of all relevant global documents in the TMF, including all required documents from vendors.
* Support results/documents disclosure of global registries.
Who Are Parexel:
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the trials of most of today’s top 50 best-selling drugs, but equally, we enable more niche drug developments that are critical to the well-being of many patients. You’ll be an influential member of the wider team.
What We Are Looking For In This Role:
For every role, we look for professionals who have the determination and courage always to put patient well-being first. That to us is working with heart.
Here are a few requirements specific to this advertised role:
* Strong clinical trial project management experience.
* In-depth understanding of project management with an emphasis on teamwork, to promote high-performance teams.
* Experience within early phase oncology studies.
* Extensive experience in clinical trial project management across international trials.
* Master's Degree ideal but not essential.
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Created on 13/02/2025 by TN United Kingdom
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