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Medical Device/Wearables Study Manager - FSP - Remote - REGISTER YOUR INTEREST

Primary Location: United Kingdom, Remote ID de la oferta R0000036236 Categoría Clinical Trials
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REGISTER YOUR INTEREST IN AN UPCOMING ROLE.

Parexel is beginning to search for an experienced Clinical Trial Manager who has experience covering Medical Device and Wearable studies.

In this role you are accountable for the deployment of digital health technologies to objectively, remotely, and continuously assess a patient over time using novel digital endpoints.

Some specifics about this advertised role

  • Ensure the digital medicine data collected across multiple studies is of the highest quality.
  • Facilitate this will require reviewing and monitoring multiple dashboards to discern if data is being collected as expected, and if there are any necessary actions or issues for follow-up.
  • Perform reviews of participant and site guides, attending meetings with vendors and study staff to ensure sites have appropriate materials for start-up and conduct, to surface or discuss any troubleshooting or site-based issues related to the digital medicine portion of the study, and to conduct any pertinent participant follow-ups.

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.

  • Bachelor’s degree and minimum 5 years of relevant global trial management experience within Medical Device, wearables studies.
  • Demonstrated interpersonal & leadership skills.
  • Ability to understand and implement the strategic direction and guidance for respective clinical studies.
  • Effective communication skills via verbal, written and presentation abilities.


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