Match score not available

Clinical Program Support Specialist

extra holidays - extra parental leave - fully flexible
Remote: 
Full Remote
Contract: 
Work from: 

Offer summary

Qualifications:

Previous experience supporting global clinical trials is essential., Understanding of project management principles with a focus on teamwork is required., Experience in early phase oncology studies is preferred., A Master's Degree is ideal but not mandatory..

Key responsabilities:

  • Provide support to and act on behalf of assigned program leads.
  • Ensure cooperation with external functions to conduct clinical trials.
  • Independently manage correspondence, complex reports, and budget overviews.
  • Address and answer complex questions from global and local trial teams.

Parexel logo
Parexel XLarge http://www.parexel.com
10001 Employees
See all jobs

Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel are currently recruiting for an experienced clinical project coordinator to join one of our key sponsors in Europe.

In this newly created position, you will be an invaluable and key member of the clinical team, you will be supporting multiple program leaders, help to drive complex global programs forward. Our sponsor building this new and exciting function with the overall goal of enhancing the effectiveness and efficiency of their global trials.

Some specifics about this advertised role

  • Provide support to and act on behalf of assigned program leads
  • Ensures cooperation with external functions (i.e. Clinical Research
  • Organizations, advisors, investigators) to conduct clinical trials
  • Independently manage correspondence, complex reports, tracking tools and budget overviews
  • Address and answer complex questions from global and local trial teams

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.

  • Previous experience supporting global clinical trials
  • Understanding of project management ethos with an emphasis on team work.
  • Experience within early phase oncology studies.
  • Masters Degree ideal but not essential.

Required profile

Experience

Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Teamwork
  • Communication

Technical Program Manager Related jobs