Senior Regulatory Affairs Associate

We are currently looking for Regulatory Affairs Professionals experienced in Clinical Trail Applications (CTAs) under EU-CTR directive. You can join us or our client dedicated projects and act as a Regulatory Affairs Consultant or Regulatory Affairs Senior Associate. This role can be based in either UK or UE (home/office based). In this role you will provide...

An opportunity for a Regulatory Efficacy Specialist to join an expanding consultancy providing global compliance and technical support to the agchem, biocide and chemical sectors. This role will focus on supporting new and renewal submission of conventional and biological compounds for PPPs. Working on a wide range of substances and products, you will...

G&L Healthcare Advisors is a fast-growing independent scientific consultancy providing Pharmaceutical and Biotechnology clients throughout the world with expert Regulatory Affairs consultancy and Quality Assurance solutions. As demand for our services and solutions continues to increase, we are looking for a CMC contractor to join our team of Regulatory...

Job Description SummaryThe UK Senior Licensing Engineer, Regulatory Affairs, based in the UK, will complete various regulatory work scopes in the UK including New Power Plant Licensing (NPPL), and work with GE-Hitachi Nuclear Energy Americas LLC (GEH) and Global Nuclear Fuels LLC (GNF) Engineering and Regulatory Affairs teams on major projects.Job...

We are looking for a Senior Consultant Regulatory Affairs for Labelling. This is a client dedicated role. The role can be based in multiple locations in UK and EU (home or office based). In this role you will partner with Label Strategist to:Conduct international labeling operations activities to support global new product and supplemental applications to...

Job Description SummaryThe UK Senior Licensing Engineer, Regulatory Affairs, based in the UK, will complete various regulatory work scopes in the UK including New Power Plant Licensing (NPPL), and work with GE-Hitachi Nuclear Energy Americas LLC (GEH) and Global Nuclear Fuels LLC (GNF) Engineering and Regulatory Affairs teams on major projects.Job...

Parexel is seeking highly motivated and experienced individuals for the position a Senior Regulatory Affairs Associate. This role can be home, or office based in various locations in Europe. As part of our team, you will have the opportunity to work within a collaborative environment and deliver services within your technical expertise. Join us and make a...

**Regulatory Affairs Consultant (Permanent) - Leading Medical Devices Consultancy - 100% remote (UK only) - £negotiable + pension, 25 days holiday + BH**: A leading medical devices consultancy is now recruiting for a Regulatory Affairs Consultant to join them on a permanent basis. **The Company**: A leading medical devices consultancy who has been...

Parexel is seeking a Regulatory Affairs Strategist (Regulatory Affairs Consultant) with extensive experience in EU, US, and ROW markets. As a Regulatory Strategist, you will play a crucial role in providing regulatory representation in cross-functional teams, developing regulatory strategies, and advising on regulatory expectations, requirements, and...

As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter - and keeping them there -your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical...

The purpose of the Global Labelling group is to drive the core labelling strategy and ensure that labelling documents are of high quality and compliant for the safe and effective use of our products for patients and healthcare providers globally. As the Global Labelling Lead, you would be responsible for developing the strategy and leading the development...

**Associate Director, Biostatistics** **Contract role with FSP** **Remote in EU** **About ClinChoice** ClinChoice is a global CRO dedicated to offering high-quality full development service to biopharmaceutical, medical device, and consumer products clients. Our services include clinical operations, project management, biostatistics, data management,...

UK CW Regulatory Affairs Manager (Inside IR35)Ensure you read the information regarding this opportunity thoroughly before making an application.This role will support one or more products from a regional regulatory perspective. * Responsible for the generation of country specific regulatory strategies and providing feedback to internal teams regarding...

Overview: Regulatory Writers provide support on the development of high quality documentation for regulatory submissions in order to help streamline the regulatory documentation process for our clients. The Regulatory Writer I (RW I) will support senior writers in the creation of a variety of documents across different service lines. The RW I will provide...

Why Patients Need You Technology impacts everything we do. Pfizer’s digital and ‘data first’ strategy focuses on implementing impactful and innovative technology solutions across all functions from research to manufacturing. Whether you are digitizing drug discovery and development, identifying solutions, or making our work easier and faster, you will...

UK CW Regulatory Affairs Manager (Inside IR35)The following information provides an overview of the skills, qualities, and qualifications needed for this role.This role will support one or more products from a regional regulatory perspective.* Responsible for the generation of country specific regulatory strategies and providing feedback to internal teams...

Overview: Regulatory Writers prepare high quality documentation for regulatory submissions in order to help streamline the regulatory documentation process for our clients. The Associate Principal Regulatory Writer (APRW) is a major contributor to document authorship for a variety of documents across different service lines. The APRW will be the project...

AL Solutions is currently seeking a highly skilled and experienced Clinical Research Associate II/Senior CRA to join our team in the Midlands region. In this role, you will play a pivotal role in overseeing and managing clinical trials for our pharmaceutical and biotechnology clients. As a CRA II/Senior CRA, you will be responsible for monitoring site...

Job DescriptionAt Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step...

**Description** **Senior Medical Writer** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our...