Company: PRA Health Sciences
Closing Date: 24 May 17
Type: Full Time
Salary (£): Competitive
Benefits: Excellent Salary and Benefits
An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA Health Sciences as a Clinical Project Manager and help realize your career potential.
CLINICAL PROJECT MANAGER
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.
For more information please see our website: www.prahs.com
Fully outsourced to a Global Pharmaceutical company, and working onsite with their team in Espoo, Finland. The Project Manager is responsible for the operational organization and management of the global cross-functional study team for complex single and multi-center, regional or global phaseII-III Oncology studies. You will ensure the timely conduct of the allocated studies according to sponsor-specific requirements (SOPs), GCP and applicable regulatory and legal requirements. Development of the study protocol and related documents together with the cross-functional study team. You will also overse selection and supervision of external suppliers in cooperation with the cross-functional team and sponsor line management, selection of clinical sites including feasibility assessment of the study together with the cross-functional team. Communication of study status and escalation of relevant deviations and issues concerning e.g. timelines, budget, recruitment, patient safety, protocol compliance is also fundamental to this role.
Desired skills and qualifications:
Scientific, medical or business degree or comparable qualification through long term work experience. At least 2 years experience of project managing global multi-center trials including oncology trials. Profound knowledge of processes and demands in clinical studies and the overall clinical development, preferably experiences in early clinical development studies. Business fluent in spoken and written English. In depth IT knowledge (MS Office). Team oriented work relations with international and cross functional contact partners as well as handling of complex work processes, competent and confident appearance; efficient way of thinking and working, organizational skills; sense of responsibility and ownership.
Together with a competitive salary, we offer a comprehensive range of benefits and an excellent working environment. As we continue to expand, there will be career opportunities on a truly global scale.
If you have any questions please email email@example.com or call our recruitment department at +44 (0) 1189 5185 63.
PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.
500 South Oak Way
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