Pharmacovigilance Manager/ Drug Safety Manager– Full Service Midsized CRO – Amazing development opportunities – France – Remote

Contenu de l'offre Pharmacovigilance Manager/ Drug Safety Manager– Full Service Midsized CRO – Amazing development opportunities – France – Remote chez Meet

Pharmacovigilance Manager/ Drug Safety Manager– Full Service Midsized CRO – Amazing development opportunities – France – Remote

Pharmacovigilance Manager/ Drug Safety Manager– Full Service Midsized CRO – Amazing development opportunities – France – Remote

Pharmacovigilance Manager (PV Manager)
€47,000 to €52,000 (Experience dependent and negotiable)
Amazing development opportunities as the company aims to double in size in the coming years

Company Background:

Opportunity to join a full serviced CRO benefitting from an extensive clinical development portfolio. This CRO has the size, agility, and structure to keep up with the needs of the market, therefore offering stability. Specialising in rare diseases and oncology, this CRO understands the importance of a patient first culture as is demonstrated by their impressive work culture. Forecasted to expand into new markets, you will undoubtedly be given the chance to grow and develop with the company. Remove the stress and worry of career development, focus on the science and this CRO will focus on you

Your role as Pharmacovigilance manager will see you:

Monitoring and managing of departmental documents, quality, workload, and resource allocation
Ensuring timely escalation of issues and concerns to the Head of Pharmacovigilance
Supporting the Head of Pharmacovigilance and assisting with review of proposals, costings for PV business and bid defence meetings
Performing departmental revenue comparison against PV team members timesheet to ensure logged time is consistent with the total professional fees for the department

Further details available upon application.

Qualifications and Skills Required:

Life science degree or equivalent (BSc, MSc, PhD)
Experience working in a CRO
Demonstratable pharmacovigilance experience
Knowledge of pharmacovigilance regulatory guidelines

Please do not hesitate to apply as this opportunity has a fast-paced interview process. Full details are available upon application. Applications are handled in line with GDPR guidelines.

Apply below or contact Britania at Meet on 020 3019 5978. Alternatively, email directly to britania@peoplewithchemistry.com

Find out more about Meet at www.peoplewithchemistry.com

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