Regulatory affairs associate jobs in Nottingham

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 ...

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. ...

Owning Projects: Responsible for project’s success, ensuring projects are delivered on-time and within budget. They are offering an exciting opportunity for a new Project Manager to join their team during a period of significant growth. Leading Project Meetings: Host project kick-offs & workshops...

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...

CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Cambridge on a contract basis for 12 months. Extensive experience in Regulatory Affairs across the UK market and an understanding of the local regulatory procedures for CTAs, MAAs and all...

Delivery Project Manager required for an International Developer and Consultancy for Renewable Energy Generation. Candidates must have 3+ years of project management experience within BESS (Battery Energy Storage Systems), Solar experience is beneficial but not essential. Suitable candidates will...

Our mission is to drive excellence in medical affairs including medical education and medical communications. We are now recruiting for a Medical Writer to join Sciterion. Sciterion – Medical communications that enable positive change in clinical practice to benefit the lives of people living wit...

Cost, Time & Resource model and oversee the preparation of the project control budget and baseline project schedule. Experienced project manager that has been involved with operation readiness, long term planning and asset management. To manage company operations and services of the assigned proj...

Lutine Bell are supporting a leading Financial Services firm in the Midlands to appoint a Prudential Compliance Officer. The ideal candidate will possess a comprehensive understanding of regulatory frameworks and compliance requirements, coupled with the ability to interpret complex regulations e...

Are you interested in working for one of the UK’s well known residential/ hospitality developer and management companies? Pillar Partnership are currently partnered with this client to help them find a Project Manager to join their team and help deliver over £800 million worth of project pipeline...

An exciting opportunity has arisen to join a boutique trading house that are looking for someone to join their compliance team in a generalist compliance officer role, there will however be a focus on the Compliance monitoring and assurance program however there will be the opportunity to get inv...

Mechanical Associate Director - £85 - 95k + Bonus + Package. I am currently working in partnership with an 100% employee owned, International MEP Consultancy who are looking to appoint a Mechanical Associate Director into their expanding London City office. As a Mechanical Associate Director, you...

Ck Group are looking for am ABPI Compliance professional to join a pharmaceutical companies Ethics and Compliance team. Support the wider compliance team to improve processes, identify risks and help drive a culture of compliance. You will support in-house medical affairs and commercial teams, he...

We're looking for a UK based Project Manager/Senior Project Engineer to join our client providing services for the Offshore/Subsea sector. Develop, review and approve project schedules and project documentation based on client requirements. Monitor and report on project process. Ensure sufficient...

Senior Medical Writer – Medical Communications – Office based 2 x week working 9-5:30pm in central London, and WFH 3 days a week working US hours of 11-7:30pm. Several years Medical Communications agency experience with a Biomedical Science degree. Independent, full service medical communications...

You will collaborate with clients to understand their objectives, develop detailed project plans, manage budgets, and oversee logistics to ensure successful event delivery. ...

Our mission is to drive excellence in medical affairs including medical education and medical communications. We are now recruiting for a Principal Medical Writer. As a Principal Medical Writer, you will develop scientific expertise across therapeutic areas, working in partnership with our Client...

BioTalent are working with a Global Consultancy business in their search for an Associate Director Regulatory Labelling for a 12 month contract. ...

The ideal candidate will have proven track record of managing multiple initiatives concurrently, delivering quality work under tight timelines; independently driving complex projects; experience guiding product/software development strategy with engineering and product teams; experience leading t...

Regulatory Affairs Manager (Parallel Import). Regulatory Affairs Manager opportunity working for a family-run pharmaceutical company that specialise in generic, OTC, medical devices, and prescription medicines. Seeking a detail-oriented Regulatory Affairs Manager with experience in Parallel Impor...

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. ...

They are seeking a Compliance Officer (VP - SVP level) in London to work within a flat structure and take the lead on their rapidly growing energy trading businesses. Advise on compliance requirements for new initiatives. Strong experience in advising businesses on energy markets compliance. ...

Role: Regional Coordinator Type: Permanent Location: Midlands We currently working with a global pharma who is looking for its next regional Coordinator to come on board within the pharma immunology department. The team is looking for highly organized, detail-oriented candidates who are strong co...

Our Client is a leading biopharmaceutical company dedicated to discovering, developing, and delivering innovative therapies that improve the lives of patients. Their commitment to excellence is reflected in our pioneering research, groundbreaking treatments, and unwavering dedication to quality a...