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Vacancy details
Vacancy description:
Job Code:
14027
Job Title:
Associate Director, Pharmacovigilance
Job Category:
Regulatory And Drug Safety
Contract:
Permanent
Discipline:
Clinical Project Manager, Drug Safety, Pharmacovigilance, Director
Country:
United Kingdom
Location:
Cambridgeshire
Min experience:
N/A
Annual salary:
Negotiable
Apply by:
04 Sep 2008
This is a key leadership opportunity for a candidate with substantial clinical drug safety / pharmacovigilance experience. Our client, a premier global contract research organisation, is an international leader in the world of clinical research and currently experiencing rapid expansion throughout Europe. They require an Associate Director of Pharmacovigilance at their Cambridgeshire office.
JOB ROLE: The Associate Director of Pharmacovigilance is responsible for assisting in the management and development of European safety management services. He/she must ensure the delivery of safety management services consistent with company SOPs/WPDs, ICH guidelines and regulatory requirements by working with Safety Managers, and liaising with other departmental personnel as required. There will also be supervisory responsibilities of Safety Managers.
PRINCIPAL REQUIREMENTS:
•Bachelor's or higher degree in Science related field, or other relevant professional background
•Relevant pharmaceutical/clinical research industry experience.
•Experience must include a proven understanding of the clinical drug development safety processes.
•Team management experience.
BENEFITS OF THE ROLE: This is an outstanding opportunity to take a leadership position with a company that is known for its supportive working environment and will give you all the encouragement and support you need to develop your career path and achieve your goals. You will be joining a truly global enterprise that offers unrivalled variety, exceptional career scope and a caring, supportive culture that nurtures the ability of every individual. Salaries are competitive and offered commensurate to the role and candidate's experience together with a comprehensive range of benefits that will ensure you achieve a quality work/life balance.
Fforde is a uniquely specialised recruitment agency/business for the pharmaceutical, clinical research and biotechnology sectors.
KEY WORDS: Associate Director, Pharmacovigilance, PVG, Drug Safety, Clinical Safety, Drug Development, Clinical Trials, Safety Management Services, Regulatory, ICH, GCP, SOPs, WPDs, Supervisory, Team Management, Degree, Science, Pharmaceutical, CRO
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