MEDICAL AFFAIRS PARTNER jobs in SOUTH EAST ENGLAND SOUTH, United Kingdom

voice matters. The Position Medical Affairs Partner - Neuroscience - Multiple Sclerosis Imagine working.... Imagine you are at Roche. You will be working within the Medical Affairs Chapter in the Roche UK affiliate. Medical Affairs...

medical affairs at relevant UK, IRL and EU/Global Meetings and communicate outputs, engage with internal and external... always looking for new ways to continue making a difference, and new people to make a difference with. We are recruiting a Medical Director...

for the role of Director, Medical Affairs for UK&IE to be responsible for Neuropsychiatry products launch activities, cross... and troubleshoot process deviations and suggest effective corrective and preventative actions. You will represent medical affairs...

Zest Scientific is actively recruiting for a Senior Regulatory Specialist in the field of medical devices for a leading... global drug development organization. We are seeking a motivated individual with substantial experience in Medical Device...

CK Group are recruiting for a Regulatory Partner (Medical Devices) to join a company in the Pharmaceutical industry... working from home/remotely. Regulatory Partner Medical Devices Role: Support the team in ensuring that regulatory...

CK Group are recruiting for a Regulatory Partner Medical Devices to join a company in the Pharmaceutical industry... is based at our clients site in Welwyn Garden City. Regulatory Partner Medical Devices Role: Support the team in ensuring...

we are looking for Do you have...? Pharmacy/Chemistry or Life Sciences degree Regulatory Affairs experience ideally with medicines, medical devices, OTCs... for the role of Regulatory Affairs Associate at our Harlow office to support European Generic new submissions via...

within the Global Regulatory Affairs, CMC Biologics, Devices department as a Director, Regulatory Affairs CMC Combination...). We have a hybrid approach to home-working! A day in the life of a Director, Regulatory Affairs CMC Combination Products... Provide...

. As an Industrial Affairs Specialist, some of your responsibilities will include: a) Manage existing and new projects development... (including Quality & Financial) in a timely and accurate manner Ensure primary documentation at the external partner companies...

implementation of medical information systems, policies and procedures. You will be a key member of the Scientific Affairs team...Posted: 4 hours ago Reference: Pharmanovia_1719525485 Title: Senior Medical Information Manager Type: Contract Full...

as a trusted and credible scientific discussion partner by engaging in scientific / medical exchange with HCPs / stakeholders... has significant expertise in key therapeutic areas, particularly within Medical Affairs or the pharmaceutical industry. Your career...

CK Group are looking for an experienced medical affairs professional to join a team of 6 working in Oncology.... This is a broad medical affairs role working with across the life-cycle with 4 products in market and a very rich pipeline over the...

CK Group are looking for an experienced medical affairs professional to join a team of 3 and work in rare diseases.... This is a broad and diverse medical affairs role working with a product launched around 18 months ago with pipeline extensions...

CK Group are looking for an experienced medical affairs professional with final signatory status to join a fantastic... team in an al encompassing medical affairs role involving both internal and external medical affairs responsibilities...

Description Kenvue is currently recruiting for: Regulatory Affairs Specialist The Regulatory Affairs Specialist... is accountable for all regulatory activities associated with their assigned medicines, medical devices, cosmetics and/or food...

, and collaborative team members to join the VEO, International medical affairs function and Team Lilly. The ­­­VEO, International... medical affairs scientist will provide strategic insight/leadership into Real World Evidence (RWE) for Lilly’s neuroscience...

would be a plus if you also possess previous experience in: Supplier Auditing and/or Quality Assurance. IVD medical device regulatory affairs... with moderate resource requirements, risk, and/or complexity. Work closely with Regulatory Affairs on deliverables for global...