Associate Clinical Trial Manager (FSP)

Parexel are currently recruiting for an experienced Oncology Associate Clinical Trial Manager.

In this position you will be the individual responsible for the coordination of clinical operations required to initiate, execute and complete clinical trials to drive on-time delivery of clinical trial milestones. May act in support or lead role

Some specifics about this advertised role

• May act as study lead and participate on the cross-functional study team.
• May act as mentor for less senior RCTO staff on the study.
• Create and maintain clinical trial documents.
• Participate in the identification, evaluation, and selection of clinical trial sites.
• Conduct data review.
• Responsible for tracking of ancillary and investigational supplies, specimens and/or imaging.
• Support CTMS and Trial Master File completeness.
• Support audit and/or inspection activities
• May manage CRO activities.

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 the 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.

• Minimum of 5 years of relevant clinical trial management experience.
• Excellent leadership, communication, and organizational skills. Able to multi-task under limited direction and on own initiative.
• Global Clinical Trial Management experience.
• Oncology clinical research experience.

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