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Position: Health Economics Manager Location: Basingstoke, UK - Hybrid Client: Pharmaceutical Type: Full-time Contract Main Responsibilities • Lead the development and delivery of HTA submissions for NICE, SMC, AWMSG, NCPE and other UK/Ireland bodies to secure national market access for the company's medicines., • Develop UK health economic and HTA strategy for new medicines and line extensions., • Manage and guide external market access agencies to ensure high‑quality dossier development., • Partner with global and regional Value & Access teams to shape economic models, SLRs, NMAs and evidence packages for the UK HTA environment., • Represent the company in HTA appraisal meetings, responding to technical and strategic questions on the economic case., • Monitor competitor HTA activity and collaborate with Medical, Marketing and RWE teams to extract insights., • Support the UK Value & Access team in developing health economic tools to drive local payer adoption., • Contribute to early pipeline planning through horizon scanning and strategic deep dives. Main Requirements • 3–5 years’ experience in a consultancy or pharmaceutical company (ideally pharma)., • Proven experience leading NICE HTA submissions, including responsibility for full dossier development and delivery., • Demonstrated track record of achieving a NICE outcome (positive or negative) from a submission they led., • Bonus: experience representing a company at NICE committee meetings., • Global HTA experience is beneficial, but candidates must have led a NICE submission with a UK affiliate. 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. • www.planet-pharma.com

A growing clinical-stage biotech is looking to appoint a Senior Manager, Regulatory Affairs to support global Oncology development programs and European Regulatory activities. Regulatory Affairs within biotech or pharma. Senior Manager, Regulatory Affairs.

Regulatory Affairs Manager – Development Strategy (Class III Devices). Regulatory Affairs professional. Embed regulatory expertise into.

In this role, you will act as a coordinator between the Group Regulatory Affairs team and local teams in expansion markets, ensuring they are aligned with Revolut's global best practices for regulatory engagement. Our Regulatory Affairs team builds transparent, high-trust relationships with regulato

Regulatory Affairs, ideally within medical devices and combination products. Regulatory Affairs Manager – Combination Product. Cpl Life Sciences is collaborating with one of the world's leading medical device manufacturers, who are looking for an experienced Regulatory Affairs Manager to support t

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

Blackfield Associates are exclusively supporting the opportunity for a Regulatory Affairs Director to lead and expand EU regulatory capability within a global CDMO environment, with a strong focus on large molecule drug substances and Biologic products. Regulatory Affairs experience, with a strong f

Freyr is a global Regulatory Solutions and Services organization supporting Life Sciences companies across Regulatory Affairs, Clinical, Safety, and Compliance. Research and apply regulatory intelligence and knowledge of strategic options to enable innovative regulatory pathways and solutions for co

Experience in Regulatory Affairs within biotech/pharma. Senior Manager, Regulatory Affairs. You’ll be supporting global regulatory activities across early to mid-stage development programs, working cross-functionally with CMC, clinical, and non-clinical teams.

This means responding clearly and on time to regulatory enquiries, as well as keeping on top of regulatory developments and monitoring regulatory change. A solid understanding of the UK regulatory environment and key regulatory compliance regimes. The Regulatory Affairs Team is responsible for maint

Regulatory Affairs Lead – Clinical Trials. We’re partnered with a cutting-edge, oncology-focused organisation delivering early- and late-phase clinical trials on a global scale, now looking to appoint a Regulatory Affairs Leader to join their growing team. As Regulatory Lead, you will play a key

Represent clients in regulatory agency interactions and provide regulatory solutions to agency objections. Direct experience preferred in providing strategic regulatory planning from early-stage development up to marketing authorisation, and a proven ability to define and deliver creative scientific

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. Experience 2 to 5 years in Regulatory Affairs.

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

The successful candidate will be responsible for leading regulatory activities for international projects, providing regulatory guidance and liaising with external partners including regulatory authorities. Minimum of 5 years experience in European Medicinal Regulatory Affairs. If you are a regulato

WEP Clinical Ltd in Greater London seeks a Regulatory Affairs Manager to oversee regulatory submissions and strategy for clinical trials. This role requires 5 years of regulatory experience and expertise in EU and FDA regulations.

The Regional Regulatory Affairs Lead will provide sound regulatory advice, support the launch & re-launch of products in an efficient manner, ensuring all formulations and product claims meet legal requirements and align with company policies. Job Title: Regional Regulatory Affairs Lead. Manage a Re

In particular, with regard to policy, legislative, regulatory and market design in the South and East region, your role will be to: Lead, develop and nurture a team of regulatory experts focusing on South and Eastern EU gases and power markets Lead on monitoring national authorities on policy, reg

The role reports to the ST&S RPT Regulatory Affairs Senior Manager Europe, with a dotted line to the Global Maritime Regulatory Affairs Advisor. Regulatory Affairs Specialist – Maritime, Biogas & Crude (Europe). Work with the EU Refining Regulatory Affairs Manager to strengthen support for ST&S RP

American Express is looking for a Regulatory Affairs and Testing professional to join their Global Risk & Compliance team in the UK. You will support regulatory interactions, manage compliance advisory needs, and liaise with various teams to uphold the compliance program effectively. A strong backgr

Quality Assurance & Regulatory Affairs SpecialistAs the Quality Assurance & Regulatory Affairs Manager, you will be responsible for building and leading the company’s regulatory and quality foundation from the ground up. The Role**As the Quality Assurance & Regulatory Affairs Specialist you will b

Gi Group is proud to be partnering with a global leader in the life sciences sector, currently seeking a Senior Regulatory Affairs Specialist to join their EMEA Regulatory Affairs team on a 12-month contract. Minimum 3 years’ experience in Regulatory Affairs or Clinical Regulatory within IVD, medi

Strong analytical capability: Demonstrated ability to develop clear, practical, and business relevant regulatory advice in complex and sometimes ambiguous legal, regulatory, and political environments. Ensure regulatory compliance capability: Enable Vodafone business functions to understand, impleme

Advance Regulatory Consulting is an innovative regulatory affairs consultancy based in the UK that provides end-to-end regulatory affairs services to the pharmaceutical industry from product development, through to licensing and post-approval maintenance. You will work under the supervision of an ex

Revolut is seeking a mid-level Regulatory Affairs Manager in the United Kingdom to enhance regulatory engagement across expansion markets. Ideal candidates will have 3+ years in regulatory affairs or compliance and demonstrate exceptional stakeholder management skills. A solid grasp of relevant regu

Lead multi-country projects and represent clients in regulatory interactions. Minimum 5 years of regulatory experience (FDA, EMA, MHRA or national authority). Proven ability to provide strategic regulatory planning from early development to marketing authorization.

Advanced Clinical is seeking a Senior Manager, Regulatory Affairs to support their clinical-stage pipeline in the United Kingdom. This hands-on role involves contributing to global regulatory strategy, preparing regulatory submissions, and interacting with health authorities across multiple regions.

The Regulatory Affairs Manager will be responsible for managing regulatory submissions, ensuring compliance, and providing expert regulatory guidance to enable timely access to medicines for patients with urgent unmet medical needs across various global markets. The Regulatory Affairs Manager will b

Regulatory Affairs ManagerLondon, United Kingdom## Join UsAt Vodafone, we’re not just shaping the future of connectivity for our customers – we’re shaping the future for everyone who joins our team. Who you are* Strong analytical capability: Demonstrated ability to develop clear, practic

Key Internal & External StakeholdersInternal* Regional Regulatory Affairs teams* R&D & Central GTNI Teams* Global Commercial teams* Marketing & NPI* Quality & Food Safety* LegalExternal** Regulatory Authorities Trade Associations Regulatory Consultants Industry Working Groupspladis is an

Lead and inspire our Regulatory Affairs team, helping everyone thrive while managing registrations, certifications, and compliance. 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 br

The Department for Environment, Food and Rural Affairs is seeking a Specialist Pay Lead to guide the development of future pay structures for the new water regulator. This role involves overseeing technical pay policy work and supporting the transition in a fast-evolving regulatory landscape.

Reporting to the Regulatory Affairs Manager, this Regulatory Affairs Associate is a key member of the Regs team within the wider Technical function. TEAMBULK ARE HIRING A REGULATORY AFFAIRS ASSOCIATE. Initiate and manage regulatory updates to packaging and digital content.

A biopharmaceutical company in Greater London is seeking an experienced Senior Manager for Regulatory Affairs, focusing on EU and ROW markets. The successful candidate must have at least 5 years in regulatory affairs and a strong academic background in scientific disciplines. This role includes mana

Multiverse is seeking a Regulatory Affairs professional to translate regulatory requirements into actionable strategies.

Expertise in scientific and technical aspects of regulatory affairs. Lead the development of regional regulatory documents and meetings in line with global strategies. Coordinate company responses to regulatory authority requests and communicate strategies effectively.

Corin Group in the UK is seeking an experienced Regulatory Affairs Specialist to support global medical device registrations and regulatory operations. Candidates should have a degree related to Life Sciences, Medical or Engineering, and possess at least 4 years of experience in medical device regul

Regulatory Affairs Advisor – Hybrid. You will be part of a team responsible for all regulatory and specification matters across product, packaging, label and documentation compliance for current UK, EU and AMEAP region legislation. If you are an experienced specification technologist looking to st

As a member of the Europe North Cluster Regulatory Affairs Team, the Senior Regulatory Affairs Associate will focus on post‑marketing regulatory activities for medicinal products within the UK and Ireland. Work on Regulatory Affairs projects & product changes to meet business needs. Carry out othe

This goal is achieved as part of an overall global regulatory approach while ensuring compliance with internal GSK process and policy and with regional regulatory requirements, delivering the best possible labeling in close collaboration with Global Regulatory Lead (GRL), Local Operating Company Reg

At least 5 years of hands-on experience in regulatory affairs, product stewardship, compliance, chemical consulting, or risk assessment. Act as a key regulatory expert across business units and cross-functional teams. Provide regulatory guidance to internal and external stakeholders, including proac

SciPro is looking for a Senior Regulatory Affairs Manager to lead regulatory strategy and compliance for AI-enabled medical software in the UK. The ideal candidate will have experience in regulatory affairs for SaMD, strong knowledge of global regulations, and excellent communication skills. Join us

Precision For Medicine in Greater London is seeking a Regulatory Manager/Senior Regulatory Manager, depending on experience. The role involves providing regulatory guidance, coordinating applications, and maintaining compliance with regulatory standards. Candidates should have a Bachelor's degree an

Assist the Head of Regulatory Affairs with regulatory meeting preparation and data packs. Set up and maintain our Regulatory Affairs AI Tooling, update the knowledge base and verify answer samples to ensure accuracy as rules change. The Regulatory Affairs team acts as the strategic guardian of Multi

Ferring+You**You will take responsibility for a range of tasks across Regulatory Affairs, Compliance, and Good Distribution Practice (GDP) as well as Good Pharmacovigilance Practices (GVP), working closely with your regulatory, quality, and safety colleagues. Contribute to monthly Regulatory Affairs

Abbexa Ltd is seeking a full-time Regulatory Affairs Officer in Bar Hill, Cambridge.