Pharmacovigilance manager - mid-size cro - uk - united kingdom, united kingdom

alessio at al solutions is currently partnered with one of europe's most well-respected mid-size cro's, who due to their continued success in early phase oncology trials are continuing their exciting expansion across europe in search of a pharmacovigilance manager to be a pivotal member of their pv team. they have seen an impressive 30% growth in 2021 and are predicted a huge 35% growth in 2022. with plans to completely double in size by 2024 - this is an opportunity to join a rapidly growing company at an exciting time!

this is an opportunity to join an innovative organisation that prides itself in its family-like culture. you will be working with some of the finest industry experts within the oncology therapeutic area, whom you will be supporting, as well as supported for your own personal career growth. if you re an experienced member of the pharmacovigilance team, looking to progress within your career, and wants to work in a fun, friendly, yet challenging environment - then this is certainly the place to be. with their huge growth plans forecasted for the next 5 years, now is the perfect time to join this thriving organization.

responsibilities:

responsible for monitoring and management of departmental documents, quality, workload and resource allocation. ensure timely escalation of issues and concerns to the head of pharmacovigilance. provide support to the head of pharmacovigilance and assist with review of proposals, costings for pv business and bid defense meetings. work collaboratively with internal and external stakeholders to ensure the pv aspects of projects are managed in line with budget, scope of work and within agreed timelines to meet clients expectations. perform departmental revenue comparison against pv team members timesheet to ensure logged time is consistent with the total professional fees for the department and the revenue is in line with pv activities performed. represent the pv department during internal meetings and external client or regulatory authority audit/inspections. generate and review departmental sops and wi and perform gap analysis. identifies new training and development opportunities for the pv department.

essential:

bsc life sciences degree or equivalent previous experience in a clinical research organisation (cro) demonstrable experience in all aspects of pv activities i.e. case processing, aggregate reporting, regulatory reporting etc. knowledge of pv regulatory guidelines previous experience in pv project management

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AL2S3 LTD
United Kingdom, United Kingdom
2022-07-06
2022-08-05
FULL-TIME
1690511
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