Medical Affairs Trainee

Looking to build your career in Regulatory Affairs?regenold Portugal is looking for a Junior Regulatory Affairs Consultant (m/f/d) to join our team in Lisbon.You will support activities across the medicinal product lifecycle, including regulatory submissions, variations, renewals and post-authorisation activities, while working alongside specialists in...

regenold Portugal is seeking a Senior Regulatory Affairs Consultant (m/f/d) to join our growing international Regulatory Affairs team in Lisbon. This senior role offers the chance to shape regulation strategies and manage complex projects independently for international pharmaceutical clients and health authorities. We require at least seven years of...

Location: Lisbon, PortugalStart date: January 2027Duration: 12 monthsWork mode: full time, hybrid (3 days onsite) About the job  As a Medical Affairs Trainee, you will support the Medical Affairs team in Portugal in bridging scientific evidence and clinical practice. You will gain hands-on experience in medical affairs, medical communication, evidence...

Location:Lisbon, Portugal Start date: January 2027 Duration: 12 months Work mode: full time, hybrid (3 days onsite)About the job As aMedical Affairs Trainee , you will support the Medical Affairs team in Portugal in bridging scientific evidence and clinical practice. You will gain hands-on experience in medical affairs, medical communication, evidence...

Sanofi is seeking a Medical Affairs Trainee in Portugal to support the Medical Affairs team with bridging scientific evidence and clinical practice. You will gain hands-on experience in medical communication, evidence generation, and cross-functional collaboration across therapeutic areas. As part of a hybrid arrangement, you will assist in planning medical...

Sanofi in Portugal is seeking a Medical Affairs Trainee to support scientific activities within the Medical Affairs team. The role offers exposure to medical communications, evidence generation, and cross-functional collaboration across therapeutic areas. You will gain hands-on experience in planning medical plans, advisory boards, and educational projects,...

Regulatory Affairs / Quality Affairs Consultant (Senior) Regulatory Affairs & Quality Affairs Remote (Worldwide) Full-time The Company The mission of Complear is to build the digital platform that becomes the operating system of Digital Health products compliance with Medical Device Regulations around the world. We want to make it easy for Digital Health...

Ctifacts is seeking a Clinical Scientist to oversee medical monitoring and support clinical trials. You will review protocols, inform feasibility activities, and train teams on the protocol to ensure high-quality execution. You will provide clinical guidance, analyze complex medical data, and participate in safety reviews to maintain trial integrity....

Regulatory Affairs Specialist - Biocide Registration Location: Portugal (remote) Competitive Salary + Benefits Scope: Our client, in the chemicals sector, is looking to strengthen its Regulatory Affairs Department due to rapid company growth and increasingly complex regulatory environments. As a Regulatory Affairs Specialist, you will be responsible for...