Offer summary

Qualifications:

Minimum of 5 years of relevant global/regional clinical trial management experience., M.S./M.A./Ph.D. or B.A./B.S./nursing degree is essential., Excellent leadership, communication, and organizational skills are required., Prior experience working at a senior level within Study Start-Up is preferred..

Key responsabilities:

Manage study, regional, or specific country level activities from study start-up through conduct and study close.

Develop and implement regional/country/study level Recruitment Strategies and Startup Plans.

Communicate with local teams, internal stakeholders, and CRO partners to ensure timely study delivery.

Oversee vendor management and coordination of vendor deliverables for assigned studies.

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.

***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

EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Required profile