Global Regulatory Submissions Senior Associate

An opportunity to join the Regulatory Affairs team at an R&D focussed global PPP company. You will:Manage a portfolio of plant protection products in specific geographical territoriesDevelop regulatory strategy Become the subject matter expert on the regulations/guidelines in your territory. As a regulatory Specialist, you will develop regulatory strategy...

Position Overview:We are seeking an experienced and driven Manager or Senior Manager, Regulatory Affairs specializing in Cell and Gene Therapy to join our team. This role will play a pivotal part in leading regulatory strategies and ensuring the successful approval and post-approval management of cutting-edge cell and gene therapy products. The Senior...

We are seeking experienced Regulatory Affairs professionals to join our dynamic team in support of a global acceleration client initiative for late-stage phase III assets. This is an exciting opportunity to play a crucial role in accelerating time to filing and approval in Global Country Initiative (GCI), emerging markets, and non-EU markets.Our global...

This job is with Autolus Therapeutics, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Role Summary With a significantly expanding regulatory team, an exciting opportunity has arisen for an experienced Senior Manager, Regulatory...

Cure Talent are delighted to be working with a well-established Medical Device company that supply and distribute innovative Medical Devices. Due to their continued growth and success, we have an exciting opportunity for a Senior Regulatory Affairs Associate to join them in West Yorkshire.As the new Senior Regulatory Affairs Associate, you will be working...

Exciting opportunity to join the regulatory affairs team at an established and highly reputable chemical regulatory science consultancy. This is expansion to cover an increasing workload. The role is delivery focussed with no commercial or business development aspects. We are looking for a regulatory person for a purely regulatory delivery role. This role...

Our client, a global pharmaceutical company, is currently looking for a Senior Regulatory Affairs Associate to join their team in Cambridge or West London (Uxbridge). This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their...

Our client, a global pharmaceutical company which develops a portfolio of prescription generic and branded pharmaceuticals within the CNS, Neurology and respiratory areas. As Regulatory Affairs Manager, you will:Preparation, submission, and management of variation applications to agreed timelinesManage and submit Renewals and PSURs in line with specified...

Our client, a global pharmaceutical company is currently looking for a EU Regulatory Strategist to join their team based on the outskirts of London on a full time, 12-month temporary basis (35 hours per week).In this role, you’ll lead and manage the operational aspects of European regulatory filings, collaborating closely with European Regulatory groups...

A prominent organisation within the clinical trials sector, focusing on early-phase studies for pharmaceutical and biotechnology clients, is seeking a talented and experienced Head of Medical Writing and Regulatory Submissions. This role offers the opportunity to lead and manage teams within a dynamic, research-driven environment, dedicated to advancing...

The client: A unique opportunity has arisen with a leading global insurance and reinsurance firm for a regulatory lawyer with an insurance sector coverage or commercial lawyer with regulatory experience.This individual will become a crucial member of the legal team, advising senior stakeholders across the business globally.Key responsibilitiesWorking as part...

Are you ready to take the next step in your regulatory affairs career? We are partnering with a leading pharmaceutical organisation to find a skilled Regulatory Affairs Specialist who is passionate about ensuring compliance and safeguarding patient safety. This exciting role offers the opportunity to work across UK, EU, and global markets, supporting both...

Our client, a global pharmaceutical company is currently looking for a EU Regulatory Specialist to join their team based on the outskirts of London on a full time, 12-month temporary basis (35 hours per week).In this role, you’ll lead and manage the operational aspects of European regulatory filings, collaborating closely with European Regulatory groups...

Due to continued expansion we are currently seeking an additional Senior Regulatory Affairs Executive to join our team in a well-established Consultancy. You would have proven success in your current role and an ambition to continually develop together with commercial awareness, a drive to innovate and be a key part of a growing company in the pharmaceutical...

G&L is seeking a skilled, mid-level Regulatory Affairs CMC professional to support the authoring of various global post-approval CMC submissions for plasma protein therapeutic products. This role is solely focused on authoring the Chemistry, Manufacturing, and Controls (CMC) sections of the Common Technical Document (CTD). Our ideal candidate has experience...

This job is with Autolus Therapeutics, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Role Summary With a significantly expanding regulatory team, an exciting opportunity has arisen for an experienced Director, Regulatory Affairs to...

Senior CRA1, Senior CRA2, or Lead Level CRAMidlands, South West, or North West Regions (Remote/Field-Based)Full-Time / Part time considered. About the OpportunityWe’re exclusively partnered with a respected leader in clinical research full service provision, as they expand their team, we are actively recruiting for Senior CRA1, Senior CRA2, or Lead CRA...

About the CompanyWe’re exclusively partnered with a respected leader in clinical research full service provision, as they expand their team, we are actively recruiting a Clinical Research Associate level 2 or Senior CRA to join their team in the United Kingdom. Our Client is known for its dedication to advancing clinical research and delivering positive...

Regulatory CMC Project Manager - Contract Partnering with an international pharmaceutical company focused on both in house product development and CDMO services, we are now supporting the appointment of a new Regulatory CMC Project Manager to oversee regulatory activities for a small molecule oncology product globally. This position will be a contract until...

Our client is a global pharmaceutical brand who are expanding their programming and statistical teams. They are currently looking for senior level (and above) programmers who will be engaged on inital 12 month contracts on a fully remote basis.Programming is the department that oversees and delivers the programming aspects of clinical drug development,...