Job Title: Project Manager EU HTA Regulations
Location: Hybrid In Brussels
Sector: Global Biopharmaceutical Company
Type: Freelance Full time contract (40 hours/week)
Contract Length: Initially until end of the year with a high chance of extension
Role Summary
A leading global biopharmaceutical organization is seeking a Project Manager to support a newly formed team focused on driving readiness for the EU Joint Clinical Assessment (JCA) process a major change in how clinical evidence will be evaluated across Europe starting in 2025.
As part of the team preparing for the evolving European Health Technology Assessment landscape, youll contribute to one of the most critical transformations in market access and evidence planning. Your work will help enable faster and more consistent patient access to medicines across the EU.
You''ll collaborate with global colleagues in evidence synthesis, health economics, regulatory, clinical development, and medical affairs. This is a highly cross-functional role with broad visibility and strategic impact.
Responsibilities:
Requirements:
Bonus if you have:
If you would like to discuss this vacancy further or to discuss your career options in confidence, please contact Femi Olubodun via telephone on +44 (0) 2039288387 or email on: folubodun@planet-pharma.co.uk
If this role isnt suitable for you, please let us know if you can refer anyone any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help!
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 recognized 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.