Senior Trial Manager, Post Marketing Study

3 weeks ago


United Kingdom Planet Pharma Full time

Planet Pharma are partnered with a global Biotechnology company who have seen an immense 91% growth this year with a trajectory to grow even more in coming years and their seeking a clinical trial manager who has experience with post marketing studies to join their team in an brand new remote position with their established team.

Requirements:

  • Experience with post marketing studies (in pharma/biotech)
  • Experience with Adverse events (AEs) and Serious AEs (SAEs)
  • Understanding of post-marketing pharmacovigilance requirements

We are looking for an experienced individual who has operational experience within post marketing studies to take on the responsibility of all operational aspects of the studies as well as the Adverse events (AEs) and Serious AEs (SAEs), Lead CRO and vendor selection and negotiation, project planning and budgeting, and have an overall impact on the companies studies.

Youll be accountable for the operational activities including the planning, conducting, and completing post-authorisation studies globally in compliance with regulatory requirements, plan, coordinate, and manage the selection and operations of CROs and other study vendors.

If interested Please click ‘ apply ’ or contact Ollie Loveland at Planet Pharma for more information:

oloveland@planet-pharma.co.uk

About Planet Pharma:

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.



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