As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.
At PRA Health Sciences, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.
At PRA, borders do not create boundaries. PRA’s success is dependent upon our ability to attract and retain a talented team of diverse professionals. Our growing workforce is comprised of over 10,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages – yet operate in unison as one worldwide PRA community.
We are currently recruiting for a Clinical Team Manager to be office-based in Stockholm area working closely together with one of our global pharmaceutical client.
Our rapid global expansion means that the pace of work here at PRA is often fast and our people are challenged daily to maintain the highest standards of best practice.
Nowhere is this more so that our Clinical Operations department and as a Clinical Team Manager you will collaborate with Project Teams to ensure that your team of CRAs is able to deliver demanding clinical trials on time and on budget.
Your role will also focus on managing the resources within the team innovatively and effectively, providing training and development opportunities to the team, performing accompanied visits, handling quality issues and supporting the delivery of the overall KPI’s.
Developing your team is also key along with pro-actively promoting communication and the sharing of ideas across departments and offices on a global basis.
You will have undergraduate degree (or international equivalent) in life sciences or health-related field from an accredited institution in addition to experience within a similar functional management role.
Substantial experience using computerised information systems including experience with PC-Windows, word processing, and electronic spreadsheets is required. Clinical trials development experience is required as is a thorough knowledge of ICH and local regulatory authority regulations regarding drug research and development.
This is a unique opportunity to give your ideas a global platform, expand your knowledge base with our cross-continent operations and, ultimately, grow your career within an expanding organisation.