Medical affairs jobs in Hertford

Background Neon Healthcare (“Neon”) is an ambitious and fast-growing pharmaceutical company that develops, produces, markets, and sells prescription only medicines to hospitals, wholesalers, and retail pharmacies. Founded by entrepreneurs with a successful track in building pharmaceutical busin...

Zest Scientific is actively recruiting for a Senior Regulatory Specialist in the field of medical devices for a leading global drug development organization. An ability to understand scientific and technical information relating to an assigned portfolio of company products. You will hold a scient...

Planet Pharma are currently partnered with a leading global pharmaceutical company who are currently seeking a Senior PV Operations Scientist to join their UK team. You’ll be a part of a great team of cross functional professionals working with various departments in the business in a proactive a...

... new role in their Regulatory Affairs team. This is a cutting edge business within the ... experience within a medical/pharmaceutical/scientific business - ideally a commercial ...

A concentration in science, engineering, medical/scientific writing, public health administration is preferred. * Minimum 2 years of working experience within Regulatory Affairs or equivalent

With a good understanding of the medical devices industry (coupled with some work in the pharmaceutical sector), you will leverage your regulatory knowledge and experience to deliver on required ...

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

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

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

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

... Medical Affairs, Commercial, Market Access, Legal, etc) and with Gilead Sciences Global RA to ensure the success of local and international business results from the regulatory point of view Local ...

A strong Regulatory Affairs background, with a good understanding of the Medical Devices industry. * The ability solve complex regulatory issues that impact the chapter and/or wider business

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

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...

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

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

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 ...

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...

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. ...

Reporting to the Senior Regulatory Affairs Officer, this role supports the Regulatory team with post-approval activities for the product portfolio. Able to demonstrate a genuine interest and knowledge of the regulatory environment and a desire to succeed in a regulatory affairs role in the pharma...

Senior Regulatory Affairs Specialist. Senior Regulatory Affairs Specialist opportunity working for a growing pharmaceutical company that specializing in medicinal, non-medicinal, medical devices, and OTC products. Due to the size of the business, a well versed Regulatory Affairs professional is r...

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...

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...