Medical affairs jobs in Huddersfield

Collaborate with the Senior Manager of Medical Engagement and the Head of Medical Affairs to develop and implement the Medical Affairs strategic and operational plan, aligning with business goals and stakeholder needs. The successful candidate will develop, communicate, and implement the Medical ...

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 Regulation, particularly in the areas of combination pr...

Associate Director, Medical Affairs. If you're a strategic innovator within Medical Affairs, this is an opportunity for you. ...

Great mix of global and EU med affairs and commercial work, across an established and growing osteoporosis account. ...

If you would like an exploratory chat about this role or the other opportunities available, please get in touch via elaine@medicaltalent. ...

Senior Regulatory Affairs Specialist to work at Corin, you will be responsible for product registration and all regulatory aspects of post-market surveillance. The Senior Regulatory Affairs Specialist will require extensive knowledge of all applicable standards, regulations, and guidance to suppo...

Senior Regulatory Affairs Specialist who will be responsible for planning, creating, and implementing solutions for regulatory registration and release of products for distribution into specific geographies. Senior Regulatory Affairs Specialist – Medical Devices & IVD’s. Minimum of 4 to 5 years p...

Associate Director Regulatory Affairs. Works with the Lead, Regulatory Affairs, and the Development Team, and with moderate/minimal supervision, with select project teams within subsidiary organizations to develop and oversee program-specific regulatory, clinical, and development strategies. Resp...

The role will encompass a large percentage of medical affairs work, as well as some promotional (and no publications!) The ideal candidate will have a blend of creative, visual experience, as well as the knowledge and confidence to work across high science accounts/projects. ...

Principal Medical Writer Opportunity. Join a dynamic and ambitious truly independent agency as a Principal Medical Writer and immerse yourself in diverse, exciting med affairs, meded and omnichannel projects. ...

You're an established Senior Medical Writer, with either Medical Affairs or Publications experience, looking for the next challenge, or an experienced Medical Writer aiming to move up. Senior Medical Writers define new directions with CMC Affinity. IPG Health Medical Communications is home to the...

Join a dynamic and ambitious truly independent agency as a Senior Medical Writer and immerse yourself in diverse, exciting meded, med affairs and omnichannel projects. ...

VP, Medical Director, CMC Affinity - UK. We are CMC Affinity, and we are hiring for an VP, Medical Director to join our global team, based in the UK. IPG Health Medical Communications is home to the world’s most celebrated and awarded med comms agencies, united by a healthy obsession with creatin...

Regulatory Affairs Advisor (Arabic Speaking). At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised ...

Regulatory Affairs Associate Manager - Cosmetics. Planet Pharma are partnered with a niche mid-sized CRO assisting them with the search for an Associate Manager, Regulatory Affairs to work on an initial 6+ month project with a focus on Cosmetic products. The Associate Manager will ensure products...

Acts as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for a stand-alone regulatory project, with guidance from senior staff as appropriate. May write new regulatory SOPs and regulatory intelligence databanks, and/or propose r...

Implements product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements. Partner with regional management and peers to ensure consistency in procedures and agency interactions Regulatory Research Main...

You will be an experienced medical writer who has worked for medical communications/market access consulting firms for several years, ideally with some people leadership/mentoring experience. New: Senior Medical Writer - Market Access / Value Communications / HEOR. A secure and steady flow of lon...

Expertise in authoring and reviewing of regulatory documents; development regulatory documents; Regulatory Strategy Plans, Clinical and Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advice and Meeting Briefing Documents, Orphan Drug and Paediatric plans/applicati...

Publications, medical communications, medical education, congress activities. If you’re an experienced writer, seeking to join a team of strong writers and have mentoring responsibilities, this could be a great fit! We’re looking for someone who has:. At least 3 years of experience working as a w...

Senior Director of Medical Strategy (Cardiovascular). A global CRO is seeking a Senior Director to join their Cardiovascular unit. This organisation is looking to welcome the new Senior Director onboard as soon as possible. ...

An opportunity for a Chemical Regulatory Affairs Specialist to join a global chemical trade association as manager of global regulatory intelligence. This is a key new hire within the Scientific and Regulatory Affairs team – you will provide regulatory support to the chemicals management and Gove...

Haybury is thrilled to announce a new partnership on a fantastic opportunity for a Senior Medical Writer. Proven experience in a Medical Writer role. Participate and develop medical education programs. ...

Medical Director/VP of Early Clinical Development (Freelance/Interim/Independent/Consulting position). Apsida Life Science are currently partnered with a growing 300 headcount SME Biotechnology that are looking to appoint a freelance Medical Director/VP to facilitate an IND submittal by EOY. Chie...