Medical affairs jobs in Reading

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...

Regulatory Affairs Specialist - Medical Device. As a Senior Regulatory Affairs Associate, you will play a crucial role in ensuring regulatory compliance for our medical devices. If you are passionate about regulatory affairs and want to contribute to the success of innovative medical technologies...

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 ...

Pharm Consulting are supporting a global Pharmaceutical group in their search for an experienced Medical Affairs professional for their Opthalmology therapy area. We are seeking applications from experienced medical affairs professionals with final signatory status for this role. The role will be...

Conducts regulatory impact assessment and provide appropriate regulatory strategy for these changes that requires regulatory actions. Working with internal concerned departments, prepares appendices attached to regulatory CMC documents to be submitted to regulatory authority and submits them. CMC...

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...

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...

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...

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 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...

You will require a strong business development background, ideally with a strong understanding of medical education or medical communications type products. I am currently looking for a Business Development Director with a strong background in business development within the IME & CME space acros...

As a Senior Regulatory Affairs Officer, you will be responsible for managing regulatory submissions in the UK and European markets including supporting over 150 product licenses. Senior Regulatory Affairs Officer. Senior Regulatory Affairs Officer opportunity working for a growing pharmaceutical ...

Due to recent success within one our Innovative Biotech Clients I am recruiting for a Regulatory Affairs manager at ICON - Working in a client-dedicated yet fully embedded role ICON’s Regulatory Strategy group, you will lead or contribute to the development and execution of the drug development s...

We are seeking a highly motivated and experienced OTC Pharmaceuticals Specialist to join our team. The successful candidate will play a key role in product development, regulatory compliance, marketing strategies, and customer support within the OTC pharmaceutical sector. Ensure compliance with r...

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. ...

Managing medical writer and junior medical writer within the team. Senior Medical Writer - Hybrid or Remote. An independent agency based in Haywards Heath is looking for a Senior Medical Writer to join their team. You will be working on a range of medical education materials and on-site events in...

Completed education in Pharmacy OR experience as a Clinical Pharmacist. ...

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 ...

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...

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 ...

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. ...

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...

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

The successful Regulatory Affairs Specialist / RA Specialist will have hands-on knowledge of FDA regulations, ISO standards & SaMD - as well as proven experience working with medical devices that use ...