Blended Learning Policy and Regulatory Specialist

OverviewMRA Search has been appointed by a rapidly expanding, Hong Kong-based asset management company to find a highly skilled Regulatory Compliance Specialist for their Cambridge office. This will be the firm's first UK Compliance hire and will suit candidates with a strong interest in crypto/web3.SalaryThe salary for this position is estimated to be...

VCLS is seeking a highly skilled Regulatory Affairs Specialist to drive forward regulatory processes, ensure compliance, and contribute to innovative clinical trials. The ideal candidate will have 4+ years of experience in Regulatory Affairs, with a focus on Clinical Trial Submissions (CTS). They will possess a deep understanding of regional and local...

We're looking for an exceptional Regulatory Specialist to join our Regulatory Affairs Team, based in Cambridge. Reporting to the respective Regulatory Manager. This role will play an essential part in ensuring the efficient co-ordination of CMR Surgical' s regulatory requirements for the UK, EU and International markets. This is a fantastic opportunity to be...

Job SummaryWe are seeking a skilled Regulatory Affairs Specialist to join our team at Vectura Group. As a key member of our regulatory affairs department, you will play a crucial role in ensuring compliance with global regulations and guidelines for medical devices and drug-device combination products.Key Responsibilities:Lead regulatory activities across...

Biochrom is part of Harvard Bioscience (HBIO), a global business providing life science, laboratory apparatus worldwide. Reporting to Biochrom QRA Manager, the **Quality and Regulatory Affairs Specialist** (QRA Specialist) supports our _in-vitro_ diagnostic product registrations, timely undertaking of post market surveillance as well as monitoring...

Proclinical are recruiting for a Regulatory Affairs Associate - II to join a pharmaceutical organisation. This role is on a contract basis and is located in either Cambridge or Uxbridge with hybrid working available. **Responsibilities**: - Conduct workflows and processes concerning document tracking, indexing, retrieving, and disseminating information to...

The Commercial and Regulatory Affairs Lead will serve as a key figure in navigating the landscape of regulatory compliance for medical technologies, thereby enabling successful research, development, and commercialisation of innovative healthcare solutions from inception to implementation for academic, clinical and SME stakeholders. This role requires an...

Welcome to Vivify Talent LimitedWe're a small consultancy with big ambitions, seeking an experienced Regulatory Document Specialist to spearhead key documents and projects. As a fully remote role, you'll enjoy autonomy and flexibility while collaborating with our passionate team.Your Key ResponsibilitiesDevelop top-tier regulatory documents, ensuring...

Role OverviewWe are seeking an experienced IT Policy Specialist to join our team at Aveva. As a key member of our organization, you will play a critical role in drafting, controlling, publishing, and training IT policies.Key ResponsibilitiesDraft and maintain IT policies, ensuring they align with business objectives.Set and track Key Performance Indicators...

The majority of the work delivered by the regulatory risk assessment team is problem-solving, working with clients to address challenging issues that they are facing with their wildlife risk assessments where standard approaches are inappropriate or insufficient. We also undertake bespoke projects for clients, such as the preparation of manuscripts and...

About the JobIn a continuous effort to grow and expand our services, ProductLife Group is looking for a Regulatory Affairs Specialist to join our team in the United Kingdom.This position plays a vital role in developing our local UK Regulatory Affairs presence, overseeing new regulatory activities related to the UK for multiple clients. You will work closely...

Job Description:As an Environmental Policy Specialist at Polytechnicpositions, you will contribute to the development and teaching of the MSt in Climate, Environment and Urban Policy programme. You will conduct original research in energy, climate systems, and sustainability transitions, identify funding sources, and build contacts in these areas. You will...

Job SummaryWe are seeking a highly experienced Regulatory Documentation Specialist to join our team at Lifelancer. As a Senior/Principal Medical Writer, you will play a crucial role in producing high-quality regulatory documentation for the international pharmaceutical industry.Key ResponsibilitiesPrepare clinical regulatory documents, including Clinical...

Proclinical are recruiting for a Regulatory Affairs Associate II to join a pharmaceutical organisation. This role is on a contract basis and is located in Cambridge/Uxbridge with hybrid working available. **Key Skills and Requirements**: - Administration familiarity within a corporate or similar business setting, preferably within a healthcare sector. -...

Do you enjoy conducting in-depth research and developing policy positions? Do you thrive on delving deep into complex policy issues and driving meaningful change? Are you passionate about shaping the future of online safety for children within the UK and internationally? If so, the Internet Watch Foundation (IWF) has an exciting opportunity for you....

Company OverviewAt Arm Limited, we are seeking a highly skilled Revenue Policy Specialist to join our team.Job DescriptionThe successful candidate will be responsible for developing and maintaining revenue policies and procedures, ensuring they are applied appropriately. They will lead the writing of technical position papers, prepare and review commercial...

Regulatory LeadershipVectura Group, a global leader in inhaled therapies and drug-device combination products, seeks a seasoned Regulatory Affairs Manager to drive the success of our medical device and DDCP regulatory activities.Regulatory Expertise: Lead regulatory activities across Vectura Group, specializing in medical devices and DDCPs, to support...

Policy Manager Location: Cambridge Salary: £50,977 to £65,005 per annum (Depending on experience) Job Type: Full-time, 2-year fixed term contract The organisations mission is to make the internet a safer space for children across the globe. They tackle this mission head-on, working tirelessly to find and remove child sexual abuse material from...

We are seeking an experienced Regulatory Affairs Specialist to join our team at Vertex Ventures HC. In this role, you will play a critical part in ensuring the regulatory compliance of our cancer therapies.As a key member of our Regulatory Affairs team, you will be responsible for developing and executing global regulatory strategies for assigned programs or...

Senior/Principal Medical WriterWe are currently looking for a Senior/Principal Medical Writer to join our team in the UK. As a key member of our clinical development team, you will be responsible for producing high-quality regulatory documents for the international pharmaceutical industry.About the Role:You will prepare a variety of clinical regulatory...