Regulatory Documentation Specialist Leader

Regulatory Document CoordinationBristol-Myers Squibb is a global biopharmaceutical company that is dedicated to transforming patients' lives through science. We are seeking an experienced Regulatory Document Coordinator to join our team.About the RoleThe successful candidate will be responsible for coordinating and authoring complex regulatory documents...

Job Title: Regulatory Documentation ExpertLocation: United Kingdom - Uxbridge, United Kingdom - CambridgeAbout the Role:We are seeking a highly experienced Regulatory Documentation Expert to join our dynamic team at Gilead Sciences, Inc. As a key member of our Medical Writing department, you will play a crucial role in authoring and reviewing regulatory...

Senior Manager, Medical Writing OncologyAbout Gilead Sciences, Inc.Gilead Sciences, Inc. is a biopharmaceutical company that aims to serve patients by leveraging its unique strengths and expertise.Job Summary:We are seeking an experienced Senior Manager, Medical Writing, Oncology to join our dynamic team. The successful candidate will have extensive...

Scientific Writing OpportunitiesBristol-Myers Squibb is a leading biopharmaceutical company that is committed to transforming patients' lives through science. We are seeking an experienced Scientific Documentation Specialist to join our team.About the RoleThe successful candidate will be responsible for authoring complex scientific documents, including...

About the Role:Gilead Sciences, Inc. is a leader in the development of innovative therapies that address some of the world's most pressing health challenges. We are seeking an experienced Associate Director to join our dynamic Medical Writing team.Key Responsibilities:Develop and author high-quality regulatory documents, including clinical study reports,...

Gilead Sciences, Inc. is a leader in the biopharmaceutical industry, seeking an experienced Associate Director to join its Medical Writing team. The successful candidate will have significant experience in medical writing and regulatory documentation, with a strong understanding of global and regional trends in the industry.The estimated salary for this...

Parexel is seeking a talented Regulatory Affairs Specialist to join our dynamic team. This role can be office or home based in various European locations.Job DescriptionDevelop strategies and plans for post-approval CMC activities such as variations, renewals, market expansions, and annual reports.Assess change controls and provide regulatory assessments of...

At Biotech 365, we are seeking a skilled Regulatory Affairs Specialist to join our team in Uxbridge. This contract role will last for 12 months and offers an hourly rate of up to £35.00 per hour (PAYE) inside IR35.Job Summary:The successful candidate will lead and manage the procedural and operational aspects of European regulatory filings within the...

About the RoleAs a Regulatory Affairs Manager, you will play a key role in planning and managing regulatory submissions (e.g., clinical trial and marketing applications) for products within our portfolio in compliance with global filing plans and local regulatory requirements.You will also be responsible for acting as a contact with relevant regulatory...

Job SummaryWe are seeking a highly experienced Regulatory Affairs specialist to join our team in support of a global acceleration client initiative. This exciting opportunity will see you play a crucial role in accelerating time to filing and approval in various markets.About the RoleThis is an excellent chance to work with a dynamic team on a mission to...

We are seeking an experienced regulatory professional to join our dynamic team as a Compliance Manager. This is a client dedicated project, and the role can be office or home based in various European locations.The successful candidate will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry,...

Lifelancer is seeking a highly qualified Principal Regulatory Affairs Consultant to join our team. As an Associate Director level professional, you will be responsible for providing expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule development.This role offers a unique opportunity to showcase your technical skills, specialist...

Proclinical are recruiting for a Senior Regulatory Consultant - Oncology to join a pharmaceutical organisation. This role is on a contract basis with the ability to work remotely from anywhere in the UK. **Responsibilities**: - Guide the development of regional regulatory documents and meetings rendering to GRT methods. - Cooperation share regulatory...

Parexel, a leading Clinical Research Organization (CRO), seeks an expert in Chemistry, Manufacturing, and Controls (CMC) for small molecule regulatory affairs. As a Principal Regulatory Affairs Consultant, you will lead post-approval CMC activities, providing strong project management skills and regulatory knowledge.This role offers flexibility with home or...

We are seeking an experienced Contract Regulatory Affairs Specialist to join our client's European Regulatory Procedural Strategist team. In this role, you will contribute to the development of European strategies, provide logistical support for meetings, and communicate regulatory information to stakeholders.About the Role:This is a contract opportunity...

About the RoleWe are seeking a talented Regulatory Management Specialist to join our team at Regeneron. This role will involve supporting the engagement of key stakeholders across Global Development functions to proactively identify process improvements, standardizations, and regulatory compliance that impacts the Regeneron Global Development quality system....

Role OverviewPark Street People is currently looking for a Senior Regulatory Affairs Manager to join their team in Uxbridge. The ideal candidate will be a confident Regulatory Lead with experience in developing and defining regulatory plans across multiple products.The role involves working closely with the regulatory team and stakeholders to provide...

Transformative Work AwaitsBristol Myers Squibb is a global pharmaceutical leader that pushes the boundaries of medical innovation. Our work has the power to transform lives, and we're looking for talented professionals like you to join our team.The European Regulatory Procedural Strategist (ERPS) role is a critical part of our organization, responsible for...

We are seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team. This role can be office or home based in various European locations.As the CMC Regulatory Manager, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls...

Job DescriptionA global pharmaceutical company in Uxbridge is seeking a Senior Regulatory Affairs Manager to join their team. The estimated salary for this role is around £70,000 - £100,000 per annum.The ideal candidate will be a confident Regulatory Lead with experience in developing and defining regulatory plans across multiple products. They will work...