Global Study Operations Manager - France or UK (Home-based) - FSP

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 experienced Global Study Operations Manager in France and the UK.

In this role, the Global Study Operations Manager will be responsible for global study activities from start up through conduct and study close. The Global Study Operations Manager has responsibility for study management aspects of assigned studies, including vendor and budget management.

These will be fully remote home-based positions.

Some specifics about this advertised role

• Global Study level implementation of Start-up and Site Activation Plans

• Responsible for global/regional study level Recruitment Strategy

• Responsible to support the development of global study level plans

• Communication with both global and local teams, internal stakeholders and CRO partner as applicable and as listed above to ensure efficient and timely study delivery of the agreed plans

• Responsible for study vendor management and oversight including follow up and coordination of vendor deliverables

• The Global Study Operational Manager will be able to work independently and exercise their own judgement.

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.

• 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.

• M.S/M.A/Ph.D or B.A/B.S/nursing degree is essential.

• Prior and demonstrable experience working at a senior level within Study start up preferred.

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