Regulatory Affairs Associate

Job Description Our client, a pharmaceutical development company has a requirement for a Regulatory Affairs Director to join their UK team. This role is perfect for a senior manager/ experienced regulatory professional who is looking to head up Strategy implantation with focus of the UK and EU market in medicinal products. As Regulatory Affairs Director,...

IQVIA have a fantastic opportunity for a Regulatory Affairs Lead to work for a growing pharmaceutical company. You will be joining a small team responsible for a range of products and therapy areas. It is a fantastic time to join the company as they are lots of growth potential and exciting plans for the near future. The role is a permanent, headcount...

Job Title: Regulatory Affairs Coordinator CTA, CTR (Consultant)Job Type: 12 Month Contract Location: Berkshire, UK – Hybrid Rate: £22-25 per hour PAYE (inside IR35)We are partnered with a leading Pharmaceutical organisation who are looking for a junior Regulatory Consultant to join on a 12-month contract basis. This role will be sat in the core regulatory...

The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe. We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products. You will grow and maintain major portfolio in...

The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe. We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products. You will grow and maintain major portfolio in...

The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territories and to register several of development projects into the international region. This role is key to driving both the Regulatory strategy and execution.• Provide...

The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe. We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products. You will grow and maintain major portfolio in...

The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe. We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products. You will grow and maintain major portfolio in...

Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA page is loaded Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA Apply locations Reading, Berkshire, United Kingdom Solna, Sweden Amsterdam, Netherlands Barcelona, Spain Sofia, Bulgaria time type Full time posted on Posted 7 Days Ago job requisition id...

The Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director – Regulatory Submissions has experience working with QRDs, CTDs, SmPC, PIL and any...

Job DescriptionAssociate Marketing Director - Multiple SclerosisThe purpose of this position is to manage the marketing and product materials as an innovative CNS pharmaceutical company prepares to introduce its first Multiple Sclerosis product to the UK market. Activities will include strategic planning and launch campaign preparation. The ideal candidate...

Associate Marketing Director - Multiple SclerosisThe purpose of this position is to manage the marketing and product materials as an innovative CNS pharmaceutical company prepares to introduce its first Multiple Sclerosis product to the UK market. Activities will include strategic planning and launch campaign preparation. The ideal candidate will have a...

The Associate Director – Regulatory Submissions The Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director – Regulatory Submissions has...

Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA page is loaded Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA Apply locations Reading, Berkshire, United Kingdom Solna, Sweden Amsterdam, Netherlands Barcelona, Spain Sofia, Bulgaria time type Full time posted on Posted 7 Days Ago job requisition id...

Associate Epidemiology Director page is loaded Associate Epidemiology Director Apply locations Reading, Berkshire, United Kingdom Rome, Italy Antwerp, Antwerp, Belgium Stevenage, United Kingdom Leeds, West Yorkshire, United Kingdom time type Full time posted on Posted Yesterday job requisition id R1419332 Associate Epidemiology Director IQVIA Real...

Job Description Associate Marketing Director - Multiple Sclerosis The purpose of this position is to manage the marketing and product materials as an innovative CNS pharmaceutical company prepares to introduce its first Multiple Sclerosis product to the UK market. Activities will include strategic planning and launch campaign preparation. The ideal...

Job Description Associate Marketing Director - Multiple Sclerosis The purpose of this position is to manage the marketing and product materials as an innovative CNS pharmaceutical company prepares to introduce its first Multiple Sclerosis product to the UK market. Activities will include strategic planning and launch campaign preparation. The ideal...

The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe. We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products. You will grow and maintain major portfolio in...

We have a fantastic opportunity for a talented Senior Associate Solicitor who is looking to take their next step towards Partnership within the Court of Protection team. We are seeking an individual who has their own client relationships and continue tonurture those relationships with a high level of service bespoke to their needs. Are you already leading a...

Associate Epidemiology Director IQVIA Real World Solutions Home-Based/Hybrid/Office-Based This innovative epidemiologist role sits in the Center for Advanced Evidence Generation (CAEG) at IQVIA and reports directly to the Chief Scientific Officer. CAEG works alongside scientific teams across IQVIA and is responsible for driving innovation in...