Trabajos medical affairs en Wokingham

As a Final Medical Signatory with proven experience within Medical Affairs you will be a leader in compliance and an ABPI code expert. Major Tasks and Responsibilities * To provide expert medical ...

For this opportunity we are seeking Medics or Pharmacists with experience and a strong understanding of the medical affairs environment and applicants with ABPI final signatory status. Previous ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

This team in embedded within the wider Medical Affairs team, which includes a field-based Medical team and a Medical Advisor based in their offices in Berkshire. The Compliance Officer operates as an ...

🏆Do you have some experience working with software as a medical device ? 🌍My client is ... Qualification in regulatory affairs or quality assurance * Knowledge of MDSAP regulations If this ...

UK based medical products business that has delivered strong growth and exceptional margins through ... Work closely with sales, clinical teams, regulatory affairs, R&D, Digital and other relevant ...

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. ...

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...

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...

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. ...

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

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...

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. ...

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. ...

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...

Planet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months regulatory experience!. Manage the operational and technical as...

Job title: Regulatory Affairs Officer. A specialty pharmaceutical business in Reading are seeking a Regulatory Affairs Officer to join their team. To ensure the product licences in the registered markets are in compliance with Regulatory requirements and manufacturing sites practice. Update relev...

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...

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...

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...