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Urgent Nursing Opportunity The Client The company have had 18% over the past 2 years and are using this to further fuel their mission of connecting patients to clinical trials through their recruitment and retention activities. Founded by industry experts, they are using digital technologies to improve the reach and accessibility of clinical trials. The Role The role we have is for a Research Nurse to support their ongoing clinical trial work dedicated to one of their site in Preston. Requirements • Registered Adult Nurse, (NMC registered with no limitations to practise), • Preferably with a background of research,, • Has completed GCP, or can complete this, • Driving license is essential due to location of the site. About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

The Regulatory Affairs Specialist role provides. Regulatory Affairs Department,. Notified Bodies and Regulatory Agencies.

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Regulatory Affairs Manager (EU) | Leading Pharma. MAA, contributing to EU regional clinical regulatory st

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. MAA, contributing to EU regional clinical regulatory strategy and supporting EU Regulatory Leads across g

Experience in Regulatory Affairs within the pharmaceutical industry. This role suits experienced regulatory professionals. Support regulatory capability and process development.

Research and apply regulatory intelligence and knowledge of strategic options to enable innovative regulatory pathways and solutions for complex global requirements and regulatory challenges. Provide critical support in developing global regulatory strategy, planning, and execution of global investi

As a Principal or Senior Regulatory Affairs CMC Consultant, you will play a key leadership role, providing high-level regulatory and technical guidance for complex therapeutics. Principal / Senior Regulatory Affairs CMC Consultant. This role is with a rapidly growing international regulatory consult

You will oversee regulatory project management and act as a key partner to global Regulatory Affairs teams, R&D, Clinical Affairs, and wider cross‑functional groups. As Regulatory Affairs Manager, you will define and deliver UK/EU regulatory strategy across a diverse portfolio of products, includi

Senior Regulatory Affairs Contractor / Consultant. Broad exposure to end to end LCM across Europe, ranging from artwork implementation through to regulatory strategy. Strong focus on process development, documentation, and regulatory compliance standards.

We're looking for an experienced Regulatory Affairs Manager to focus on financial crime related regulatory engagements, ensuring communication with external regulators is transparent, compliant, and efficient. The Regulatory Affairs team builds transparent relationships with regulators to keep Revol

You’ve built experience in a regulatory or quality-focused admin role, and you take pride in keeping things accurate, organised, and audit-ready. You’ll support the quality and regulatory teams with keeping their processes and procedure in good shape. Ensuring processes related to quality/regula

You will sit within the wider Regulatory Affairs team and will work very closely with the Regulatory Affairs Director for Colonis. While the role is not primarily client-facing, you will engage directly with regulatory authorities, including participation in agency meetings The role requires someone

The Regulatory Affairs Specialist reports into RA leadership and is responsible for regulatory compliance, regulatory submissions, and supporting regulatory planning and execution across the organisation. We are seeking a Regulatory Affairs Specialist with hands-on experience in software medical dev

Are you an experienced regulatory professional looking to shape global strategy and influence product development at an international level? This is an exciting opportunity to a global Pharmaceutical Manufacturing organisation as an Associate Director, Global Regulatory Strategy. Review regulatory d

Associate Director – Regulatory Affairs CMC. CMC regulatory strategy across development and lifecycle programs. CMC regulatory documentation and CTD Module 3.

Freyr is a global Regulatory Solutions and Services organization supporting Life Sciences companies across Regulatory Affairs, Clinical, Safety, and Compliance. Title : Regulatory Affairs Associate - Regulatory Operations - Publishing. We partner with leading pharmaceutical, biotechnology, and medic

Halianis currently recruitingfor an experienced Reg affairs Risk Management specialist for a manufacturing client in theCotsworlds. Location: UK (multi-site flexibility)Industry: Medical DevicesEmployment Type: Full-time, PermanentA leading UK-based medical device manufacturer is seeking an experien

It serves as the primary point of contact for regulatory and product safety matters, supports business decisions through impact assessments, and drives harmonization of stewardship processes, SDS, labeling, and regulatory proje. This role provides product stewardship and regulatory support for the C

Where appropriate, to act as the CMC Regulatory Lead on CMC Teams, representing the CMC Regulatory viewpoint and expertise on the CMC Team;* To identify potential CMC regulatory risks to the strategic / operational plans and propose options to mitigate risks;* To plan, prepare, review CMC component

Regulatory Affairs & Quality Control Executive. Quality Control and Regulatory Affairs experience preferred but not essential. Compiling Regulatory dossiers for worldwide submission and liaising with Export customers.

As Director, Litigation, Competition & Regulatory Affairs, EMEA, you will be the primary litigation, competition and regulatory counsel for the Sony Interactive Entertainment (SIE) business in the EMEA region, including Europe and the UK. You will handle a wide range of litigation matters, working c

We are looking to hire a Legal Counsel to join our Public Affairs & Regulatory team. An interest in politics and current affairs, keeping informed about the regulatory environment. Your primary focus will be to help maintain Trustpilots reputation as a trusted and compliant platform by navigating a

Maintain and organize regulatory documentation including job descriptions and resumes regulatory submissions correspondence with regulatory agencies and regulatory tracking databases. Collaborate with regulatory affairs teams to ensure alignment of training programs with current regulatory expectati

Tether is seeking an experienced and visionary Head of Regulatory Affairs to design and execute global regulatory affairs strategies for our Tether Data business vertical. Expertise in preparing complex regulatory documents and other major regulatory submissions, including the preparation and execut

A prominent pharmaceutical company in the United Kingdom seeks a Regulatory Affairs Specialist to provide full regulatory support for products. The ideal candidate will have significant experience across the product lifecycle, particularly with CMC regulatory submissions.

The role will lead the regulatory team, interfacing with regulatory agencies like the MHRA, EMA, FDA, preparing and submitting regulatory documents, and managing risk. Lead training and mentorship initiatives within the regulatory affairs team, fostering regulatory expertise and growth within the or

Graduation in pharmacy background or any relevant degree.Supervision and motivation of national approval team members.Contact person for all team members.Proactively ensuring smooth team operations and effective collaboration.Creating an inspiring team environment with an open communication culture.

The Regulatory Affairs Lead provides expert telecoms and digital regulatory guidance across these lines of business, and acts as a key subject‑matter expert (SME) in implementing the Group Telecom Regulatory Compliance Policy. Accountable for Group Regulatory Compliance Policy Framework. Responsib

Provide ongoing regulatory support to the regulatory affairs team lead and project teams to ensure regulatory concerns are addressed and relevant data is generated to meet project objectives. Review tasks, support, and mentor Regulatory Affairs associates. Contribute to regulatory documents and repo

Maintain and organize regulatory documentation including job descriptions and resumes regulatory submissions correspondence with regulatory agencies and regulatory tracking databases. Collaborate with regulatory affairs teams to ensure alignment of training programs with current regulatory expectati

A leading fintech company is seeking a Head of Legal to provide practical legal guidance and support across corporate governance, commercial contracting, and regulatory compliance. This role requires a qualified solicitor with significant experience in financial services and expertise in technology

Author and/or review compliant digital device documentation for Health Authority submissions, applying agreed digital device global regulatory strategies, current regulatory standards and guidelines. Regulatory Affairs and other functional areas. Demonstrated practical experience in digital device r

Who you are*** Strong analytical capability: Demonstrated ability to develop clear, practical, and business relevant regulatory advice in complex and sometimes ambiguous legal, regulatory, and political environments. Manager Regulatory Affairs #J-18808-Ljbffr. Regulatory Affairs ManagerLondon, Unite

A global entertainment leader is seeking a Director for Litigation, Competition & Regulatory Affairs in the EMEA region. Candidates should possess a Juris Doctorate, excellent collaboration and communication skills, and substantial experience in regulatory environments. The role involves advising on

A leading pharmaceutical organization is seeking a Regulatory Affairs Manager to support product development and lifecycle activities. The role involves leading EU regulatory submissions, contributing to clinical regulatory strategies, and ensuring compliance.

Keep the heartbeat of innovation running and join our client in this Regulatory Affairs Labelling position and ensure cutting-edge pharma operations never miss a beat!. Proclinical is seeking a Regulatory Labelling Manager to support the development, optimization, and implementation of regulatory la

As Director, Litigation, Competition & Regulatory Affairs, EMEA, you will be the primary litigation, competition and regulatory counsel for the Sony Interactive Entertainment (SIE) business in the EMEA region, including Europe and the UK. You will handle a wide range of litigation matters, working c

A leading telecommunications company is seeking a Regulatory Affairs Lead in Greater London.

A clinical-stage biopharmaceutical firm in the United Kingdom is seeking a Director, Regulatory Affairs CMC. The successful candidate will leverage a minimum of 10 years of experience in Regulatory Affairs, involving detailed knowledge of large molecule biologics and FDA/EU regulations. This leaders

The ideal candidate should have a degree in a scientific field and substantial experience in regulatory affairs. A recruitment agency in pharmaceuticals is seeking a professional for a mid-senior level role focusing on regulatory input for product submissions. You will manage complex regulatory subm

Experience in medical device regulatory affairs (MDD, MDR, IVDD, IVDR, UK MDR, ISO 13485). Are you passionate about regulatory affairs and want to play a key role in bringing innovative medical devices to market? Join our growing, dynamic team where your work directly impacts patient safety and heal

A leading financial services group is looking for a Head of Regulatory Affairs in Greater London. The role involves maintaining relationships with UK regulators, providing strategic advice, and ensuring compliance with regulatory requirements.

A leading pharmaceutical company in the United Kingdom is seeking a Mid-Senior level Regulatory Affairs Specialist to provide regulatory input and support for new Marketing Authorisation Applications. The ideal candidate will have a strong background in regulatory submissions and CMC, with an emphas

A governmental energy regulator in the UK seeks a confident leader to play a central role in protecting energy consumers and supporting the transition to a sustainable energy system.The successful candidate will lead multidisciplinary teams to deliver high-quality work in compliance, enforcement, an

The individual will lead projects, collaborate with cross-functional teams, and ensure compliance with regulatory standards.