Medical affairs jobs in Camberley

Implement product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements and manage the development of the regional product label by collaborating with the Labeling Working Group. CK Group are recruitin...

Lead and develop medical affairs strategy plans for all areas of medical affairs. 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 a...

Lead and develop medical affairs strategy plans for all areas of medical affairs. 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 v...

Our clients are now seeking an experienced Medical Affairs Learning & Development professional to join their team and to be responsible to identify and address learning needs for Medical Affairs globally for processes and operating models, and to collaborate and partner with MA Functions to lead ...

This Senior Medical Director role is the Global Medical Affairs Asset Lead for a recently acquired compound. Alongside the cross functional Asset Leads and as part of the Asset team, you will be accountable for developing and delivering the Global Medical Affairs strategy in order to achieve the ...

Reporting into the Head of Technical and as the manager of the Compliance team, the key purpose of this role is to ensure the compliance of Synergy products to both legal and customer expectations, and the provision of timely and accurate data to customers/3rd party organisations to support this....

The purpose of the Regulatory Affairs Associate/Senior Associate role is to manage the operational and technical aspects of regulatory affairs for the UK and Ireland marketing affiliate and the Maltese marketing affiliate, including:. At least one year industry related experience in regulatory af...

Based in the UK, the Regulatory Affairs Associate is expected to;. Keeping up to date with regulatory and legal changes in EU. Preparing pre- and post-authorisation regulatory documentation and applications. Providing general regulatory advice to company's staff. ...

Are you an ambitious healthcare advertising Account Director? My client requires an AD capable of building and shaping creative marketing strategy for global healthcare brands. ...

Senior Medical Writer – Medical Communications. Senior Medical Writer – Medical Communications. Position: Senior Medical Writer. Serve as the medical writing representative on assigned project teams, providing proactive support to project leadership for planning efficient work plans and timelines...

As a Principal Medical Writer at Real Chemistry you will be working across several therapy areas to create a range of material, ensuring the language and content is appropriate for the target audience. Medical Writing role within an agency environment. ...

Senior Medical Writer - Global Med Comms Agency - Remote, UK. Phenomenally excited to be partnering with my Global Med Comms Agency client to support them in their search for a Senior Medical Writer to join thriving their UK team. We are looking for a Senior Medical Writer, ideally from a Med Com...

Role: Senior Director, Regulatory Medical Writing. Manage a team of internal medical writers (direct reports). At least 10 years of relevant medical writing experience is required. ...

BioTalent is delighted to be partnered with a innovative Health Technology company based in the UK and we are on the hunt for Medical Director to join the team on a full time basis. Demonstrated experience in medical leadership or medical affairs roles within Health Tech. Provide medical leadersh...

Regulatory Affairs Specialist - Lifecycle Maintenance. We are seeking an experienced Regulatory Affairs Specialist to oversee lifecycle maintenance for our mature product portfolio. The successful candidate will manage compliance activities, coordinate with EU member states under the MRP, handle ...

This internship programme will help you build a fantastic online medical portfolio. This internship provides you with all the opportunities to grow - both within your role as a writer/editor and, more generally, as someone navigating the vast plain of career development. I have joined Klarity Hea...

The candidate needs to have relevant experience as Medical Science Liaison or Medical Advisor. Join us as Medical Science Liaison and be the catalyst for a healthier tomorrow!. Planning, organization and participation in Medical Education activities: Build medical education programs with scientif...

Are you a seasoned Senior Medical Writer with a passion for scientific publications, client interaction, and communicating complex scientific messages? Want to take the next step in your career and be part of a dynamic and supportive environment where your contributions make a difference?. This S...

The successful Medical Science Liaison will be working with the medical team to communicate evidence based scientific, technical and development matters with customers and stakeholders. Acting as the field scientific / medical expert, delivering medical education, updates and gathering insights a...

We are recruiting for a Regulatory Affairs Manager - EU. The role reports to Director of Regulatory Affairs and is based in our offices near High Wycombe managing a small team. This role is responsible for regulatory efforts for EU and UK products, particularly post-Brexit, where the Marketing Au...

Do you have a passion for publications? How about a Senior Medical Writer role with one of the most rewarding and supportive, independent MedComms agencies?. You will need to have at least 3 years' experience writing for a Medical Communications agency, including publications, and be based in the...

Title: Global Learning & Development Lead - Medical Affairs Company: Global Pharmaceutical Company Location: Hybrid Role (50% WFH - Addlestone Office) Type: Permanent - Full-time Summary: Planet ...

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

... medical products. * Contributing regulatory guidance in order to enhance product development ... Previous experience in Regulatory Affairs and Compliance particularly within pharmaceutical ...