Country Study Operations Manager (Unblinded) - UK/Europe - FSP, Uxbridge
Client:
Parexel
Location:
Uxbridge, United Kingdom
Job Category:
Other
EU work permit required:
Yes
Job Reference:
78ec31ddea24
Job Views:
6
Posted:
02.04.2025
Expiry Date:
17.05.2025
Job Description:
When our values align, there's no limit to what we can achieve.
Parexel is currently recruiting for an experienced Local/Country focused Study Operations Manager (Unblinded) based in either the UK or Europe. (Previous unblinded trial experience is not necessary).
In this role, the Country Study Operations Manager (Unblinded) will be responsible for study and country level activities from start-up through conduct and study close. The Country Study Operations Manager has responsibility for study management aspects of assigned studies, including vendor and budget management.
This will be a fully remote home-based position.
Responsibilities:
1. Regional/Country/Study level implementation of Start-up and Site Activation Plans
2. Responsible for country/study level Recruitment Strategy
3. Support the development of study level plans
4. Communicate with the local team and internal stakeholders and CRO partner to ensure efficient and timely study delivery of the agreed plans
5. Manage and oversee study and/or country vendor management including follow-up and coordination of vendor deliverables
6. Work independently and exercise own judgement
About 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:
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:
1. Minimum of 5 years of relevant clinical trial management experience.
2. Excellent leadership, communication, and organizational skills. Able to multi-task under limited direction and on own initiative.
3. M.S/M.A/Ph.D or B.A/B.S/nursing degree is essential.
4. Prior and demonstrable experience working at a senior level within Study start-up preferred.
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