PRAHS 2017-40388 in United States

Be part of our exciting new strategic partnership!

PRA Health Sciences is a top 5 CRO and winner of CRO of the year for Europe, Asia and North America in 2015 and 2016.

Our strategic partner is is one of the world’s premier innovative biopharmaceutical companies.

Embedded within our newest strategic partner and reporting to the Director of Clinical Operations, you will be a highly motivated and dynamic project management professional with a strong commercial knowledge of the pharmaceutical industry, a positive attitude and ambition to make things happen. You will need to be a natural leader with excellent communication skills to succeed in the role of Clinical Study Manager. You must be able to set goals and achieve them by motivating your team and building strong relationships with a diverse range of both internal and external customers. Candidates applying for this position will have a life science degree or similar, in addition to having experience of managing global clinical studies.

This position can be office based or home based in any European country

What will you be doing?

As a Clinical Study Manager, you will manage the Operational Study Management for 1 or more studies of moderate complexity generally with responsibility for all study management aspects of assigned studies. You will be accountable for the development of realistic detailed study startup and monitoring plans, lead study risk planning, lead inspection readiness activities and be accountable for the delivery of the study against approved plans. You will have study management oversight, be the study team interface and be the subject matter expert for study management systems and processes.

Training and Education Preferred:

  • Extensive global clinical trial/study management experience

  • Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations

  • BS/Nurse – minimum of 5 years relevant experience

  • MS/PhD – minimum of 3 years relevant experience

Prior Experience Preferred:

  • Demonstrated study management / leadership experience

  • Demonstrated oversight of CROs


  • Understands how to work with vendors to accomplish tasks

  • Ability to interpret study level data & translate and identify risks

  • Ability to proactively identify & mitigate risks around site level in study execution

  • Understands feasibility of protocol implementation

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

ID: 2017-40388

External Company Name: Pharmaceutical Research Associates, Inc

External Company URL: