Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Study Operations Manager I/II - FSP
Job ID R0000032441***Note: this role will be heavily focused on Study Start-Up activities & while it is not required, unblinded experience is highly preferred***
Parexel is currently recruiting for an experienced Study Operations Manager.In this role, the Study Operations Manager will be responsible for study, regional or specific country level activities from study start-up through conduct and study close. The Study Operations Manager has responsibility for study management aspects of assigned studies, including vendor and budget management.
Some specifics about this advertised role
Regional/Country/Study level implementation of Startup and Site Activation Plans
Responsible for regional/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 Study Operational Manager will be able to work independently and exercise their own judgement.
Who is 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 global/regional 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
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