Study Operations Manager

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 Local/Country focused Study Operations Manager I.

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

This will be a fully remote home-based position.

Some specifics about this advertised roleRegional/Country/Study level implementation of Start up and Site Activation Plans Responsible for country/study level Recruitment Strategy Responsible to support the development of study level plans Communication with the local team and 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 and/or country vendor management and oversight including follow up and coordination of vendor deliverables The Country Study Operational Manager I 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. Not quite the role for you? Join Our Talent Community and we'll reach out with job alerts when positions that match your career interests become available. We'll also share periodic updates about the latest company news and events. Sign up today
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