Trabajos medical affairs en Jarrow

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

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...

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

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. ...

Remote Senior Regulatory Medical Writer working through an FSP model for a Global Oncology focused Pharmaceutical Company. The Principal Medical Writer I is responsible for developing clinical documents for submissions to regulatory authorities globally. Oversees the medical writing activities of...

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...

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...

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...

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...

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...

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. ...

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...

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. ...

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...

Working with the regulatory team (and core stakeholders across multiple areas), your role will be to operate as a Regulatory Lead, providing centralised regulatory strategy and guidance across the region and make sure that regulatory deadlines and approvals are achieved. A global pharmaceutical c...

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 ...

Medical Science Liaison – Nephrology / Rare Diseases. Providing medical information and responses to complex medical questions from clinicians. Working as part of a wider team, but with sole responsibility for specialist centres across UK, Netherlands and Ireland from a medical affairs standpoint...

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...

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

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...

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. ...

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...

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...