Enable job alerts via email!

Clinical Trial Leader - Phase I Oncology - FSP - Remote

Parexel

Uxbridge

Remote

GBP 80,000 - 100,000

30 days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

An established industry player is seeking an experienced global trial manager to lead Phase I Oncology trials. In this pivotal role, you will be responsible for the planning, execution, and delivery of clinical trials, ensuring compliance with regulatory standards and focusing on patient value. Your expertise in project management and teamwork will drive high performance within the clinical delivery team. This position offers the opportunity to make a significant impact on the clinical landscape and contribute to the advancement of innovative therapies. Join a dynamic team committed to prioritizing patient well-being and delivering excellence in clinical research.

Qualifications

  • Strong project management experience in clinical trials.
  • In-depth understanding of teamwork and high-performance teams.

Responsibilities

  • Accountable for planning and operational feasibility of trial timelines.
  • Maintains oversight during clinical trial conduct ensuring compliance.

Skills

Clinical Trial Project Management

Teamwork

Risk Mitigation

Patient Engagement

Education

Masters Degree

Job description

Parexel are 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, you are accountable for the set-up, execution and delivery of your assigned trials and contribute to 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.
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 team work, to promote high performance teams.
  • Experience within early phase oncology studies.
  • Extensive experience in clinical trial project management across international trials.
  • Masters Degree ideal but not essential.
Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.