Medical affairs jobs in IsleworthCreate job alerts

An amazing opportunity for a GU & Lung Medical Advisor to join a high performing Oncology team , my client are looking for a Medical Advisor for a 12 month contract who will be based at their offices in London 3 days per week. You must have experience working within Oncology and knowledge of the ABPI conduct , you will be involved in strategy , training , budget and have exposure of working with global teams This is a really great opportunity for an experienced medical Advisor or someone who is looking for an opportunity within this type of role STRATEGY: • Act as UK/Ireland Medical Affairs expert for the Oncology business, • Support the leadership team in the development of Oncology Brand strategies and implement the Medical Tactics OPERATIONS: • Develop Medical materials, review marketing materials and trainings, • Ensure scientific and clinical accuracy for a specific product or brand, • Develop KTL scientific interaction plans (national level), • Support and conduct internal training and ensure continuous education of team members and new employees, • Provide support in planning and tracking of the Oncology medical budget, • Comply to relevant training and SOPs, • Maintain up-to-date GxP knowledge DATA GENERATION AND SCIENTIFIC COMMUNICATION: • Lead or support medical studies, assist coordination of local clinical projects and aid site selection, • Lead Local publication process and dissemination aligned with local, regional and global publication plan, • Anticipate, interpret and share medical information with stakeholders STAKEHOLDER ENGAGEMENT: • Provide training to HCPs and support in Medical educational events, • Identify and interact with key members of the medical community and other healthcare stakeholders with pre-defined metrics, in accordance with local regulations EDUCATION: • University degree in Pharmacy or Medicine advantageous; Secondary / advanced scientific degree (e.g., MSc, PharmD, PhD, DO, MD) preferred, • Scientific and / or clinical training in area of relevance to position strongly preferred, • Other advanced degree (non-scientific) and/or business degree/training is advantageous, • UK ABPI signatory experience and knowledge and experience of UK ABPI Code of Conduct WORK EXPERIENCE: • Prior pharmaceutical industry experience & knowledge of regulatory environment, • Experience specific to Oncology preferred, • Substantial professional, clinical or research experience in a scientific or related field advantageous, • Knowledge and experience of methodology of clinical research and Good Clinical Practice preferred, • Knowledge and experience in project management

Design Quality Engineer CY Partners are partnering with a growing and innovative diagnostics organisation to appoint a Design Quality Engineer into their Regulatory Affairs team. This is a key role supporting the development of IVD products, with a strong focus on Design History File (DHF) ownership, design controls and audit-ready documentation. It is a great opportunity for someone who enjoys combining technical quality expertise with cross-functional collaboration in a fast-paced, project-driven environment. The Opportunity You will take ownership of DHFs from project initiation through to completion, ensuring all design and development activities are planned, documented and compliant with regulatory standards. Working closely with the programme management function as well as the wider technical teams, you’ll play a central role in ensuring projects are delivered with robust traceability, strong documentation and right-first-time quality. Key Responsibilities • Own and manage the end-to-end DHF lifecycle for IVD projects, • Author and coordinate key documentation including design plans, inputs/outputs, verification & validation and design reviews, • Ensure full traceability across requirements, risks and testing activities, • Support and facilitate design reviews, ensuring clear documentation and action tracking, • Collaborate cross-functionally to ensure DHF deliverables align with project timelines, • Ensure compliance with ISO 13485, design control requirements and internal QMS processes, • Support audit readiness, including preparation of DHF evidence packs and participation in inspections, • Contribute to continuous improvement of SOPs, templates and quality processes About You • Degree qualified in a Life Sciences or related discipline, • Experience in Quality Engineering or Design Quality within medical devices or IVD, • Proven experience owning or contributing to Design History Files (DHF), • Strong understanding of design controls and ISO 13485, • Confident working with controlled documentation systems (eQMS/SharePoint), • Able to work cross-functionally and manage competing priorities in a fast-paced environment Desirable experience includes: Exposure to FDA 21 CFR 820 and/or IVDR/UKCA requirements Risk management (ISO 14971) and audit support experience This is a chance to join a business at an exciting stage of growth, where quality and regulatory excellence are central to product development. You’ll have real ownership, visibility across projects and the opportunity to contribute to impactful diagnostic programmes. For more information or a confidential discussion, please get in touch. CY Partners is acting as an Employment Agency in relation to this vacancy. Applicants must have the full right to work in the UK.

Nordberg Medical AB is looking for a Key Account Manager for JULÄINE™ covering the South West region in the UK. You will own sales and business development within your territory, collaborating closely with the Sales, Marketing, and Medical Affairs teams.

You will report to our UK Sales Manager, and collaborate closely with Sales, Marketing and Medical Affairs to develop and implement sales strategies. As our Key Account Manager for JULÄINE™ covering the South West region,. Nordberg Medical is a Swedish biotech pioneer in biostimulation, bringing

Ferring Pharmaceuticals is seeking a Medical Advisor to report to the Medical Director, UK & Ireland.

As our Key Account Manager for JULÄINE™ covering the South West region,. You will report to our UK Sales Manager and collaborate closely with Sales, Marketing and Medical Affairs to develop and implement sales strategies. Account Management and Sales experience in the UK medical aesthetics market

Cure Talent are delighted to be partnered with an innovative medical technology company transforming access to ear and hearing healthcare. Operating at the intersection of medical devices and software, the business is scaling its global presence and is now looking to appoint a Head of QARA to take ownership of Quality & Regulatory strategy and delivery. This is a senior, hands-on leadership role, responsible for defining and executing the pathway to market for a Class IIa device across the US, UK and Europe. You will lead the QARA function, own regulatory approvals, and ensure quality and compliance are embedded across the organisation as it continues to grow. Key Responsibilities Own and lead the Quality & Regulatory Affairs function, with full accountability for delivery, performance and outcomes. Define and deliver the regulatory pathway to achieve FDA clearance and CE marking for a Class IIa medical device across the US, UK and EU. Act as the accountable owner for regulatory submissions and authority interactions, leading engagement with FDA, notified bodies and other regulatory agencies. Build, structure and scale the QARA function, while leading and developing the team. Maintain and improve the Quality Management System in line with ISO 13485, FDA 21 CFR Part 820, EU MDR and EN 62304. Drive CAPA, non-conformances, change control and audit activity, ensuring effective implementation and closure. Oversee Technical Documentation and Design History Files to support global submissions. Ensure compliance of SaMD, embedding software lifecycle requirements across product development and the QMS. Lead audits and inspections, managing interactions and responses. The Ideal Candidate Will Have Proven experience leading Quality & Regulatory functions within the medical device industry. Proven experience within a growing or scaling MedTech start-up environment. Proven experience delivering FDA 510(k) and EU MDR approvals for medical devices. Experience bringing medical devices to market, with ownership of regulatory pathways and outcomes. Strong knowledge of ISO 13485, IEC 60601 and IEC 62304, with experience across audits, technical documentation and design controls. TPBN1_UKTJ

Our Medical Science Liaisons (MSLs) are field-based medical affairs professionals covering various countries or regions across Europe. This is an exciting opportunity to be part of the passionate, high-profile, high-impact Medical Affairs (MA) team, and work in a dynamic and collaborative setting. M

With a deep interest in science and medical communications, we believe someone with the following qualities and experience could be a good match for this role:. Previous experience as an Account Director within a medical communications agency or similar.

Strategy & Medical Affairs team. Medical Affairs, and driving cross-functional transformation. Drive operating model, capability, and Medical Affairs strategy work.

Oversee the development of a wide range of medical affairs materials, including medical education content, publications, scientific platforms, training resources, and congress materials. Pharma-Partners are currently supporting a global, life science consultancy seeking to appoint a Senior Manager t

BioTalent is seeking a Manager for its Strategy & Medical Affairs team in Greater London. With a strong Medical Affairs background and over 6 years in strategy consulting, you will influence decision-making at senior levels. This role offers fast progression and opportunities to shape the practice o

Novo Nordisk in England is seeking a Senior Manager in Medical Affairs to lead the medical strategy for rare endocrine and blood disorders. Candidates should be a registered medical practitioner or pharmacist with significant knowledge of rare diseases, coupled with extensive experience in medical a

We are seeking an experienced, passionate, and people-focused Medical Affairs Clinician to join our Medical Affairs team, reporting to the Head of International Medical Affairs. Develop peer-level relationships with medical and scientific experts, interpret and effectively communicate relevant medic

The Medical Affairs Lead oversees managing all aspects of the planning, development, and execution of resources and strategies that support and drive the client’s Medical Affairs business. The Medical Affairs Lead will work across the Syneos Health organization in tandem with other functional area

Practice Area Lead, Medical Affairs Communications**Reporting to the Head of IQVIA Medical Communications, this role is accountable for the strategic growth and management of our flourishing Medical Affairs Communications practice, leading a team of 18 Account Handlers to achieve strong customer rel

Medical Grants, Medical Affairs Operations, or Medical Governance. Medical Grants, governance frameworks, and operational excellence within Medical Affairs. IMED & Medical Scientific Grants.

Autolus Limited is seeking an Executive Medical Director to lead the Medical Affairs strategy for oncology products in the UK. A degree in Bpharm is required, along with solid industry experience in medical affairs, particularly in hematology or oncology.

The ideal candidate will have a medical background, significant experience in Medical Affairs or Clinical Development, and a strategic mindset. A leading global pharmaceutical company is seeking an experienced Executive Director to lead medical affairs strategies across critical programs. The role i

Co-develop plans for evidence generation, medical launch plans, MSL / Field Medical Affairs strategy, medical education programs, scientific publication planning and Medical Expert network development with TAs. Represents a credible and cohesive medical voice, integrating US and International Medica

Dexcom in the United Kingdom seeks a Senior Medical Affairs Specialist based in the UK North territory. This role involves engaging with healthcare professionals, delivering medical education on CGM technology, and responding to inquiries with evidence-based information.

Theramex Germany GmbH is looking for a Senior Manager in Global Medical Affairs to lead the development of medical strategies that align with business objectives and ensure compliance. The ideal candidate will have a medical degree or equivalent and experience in Medical Affairs, with a strong focus

This role involves managing Medical Affairs programmes for global pharmaceutical industry clients, requiring expertise in project management and communication.

A leading life sciences services organization is seeking a Clinical Project Manager II to manage interdisciplinary clinical research projects.The ideal candidate will have a Bachelor's Degree in life sciences or equivalent experience and a strong understanding of Good Clinical Practices.Responsibili

Project Leadership and Delivery.Manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance with GCP, relevant SOP’s, and regulatory requirements.Acts as a primary liaison between the Company and the Customer to ensure timely study launch, c

General Description:**The Director, Global Medical Affairs – Hematology, within Global Medical Affairs (GMA) is responsible for executing the global medical plan across the hematology portfolio and pipeline. The Director manages medical activities throughout the product lifecycle in collaboration

A leading healthcare organization in the UK is seeking a Medical Advisor to provide strategic medical leadership and support to internal teams and stakeholders. As the local medical expert, you will lead the delivery of the local medical plan and engage external experts. Ideal candidates will be GMC

A leading global healthcare organization is seeking an Executive Medical Director for Global Medical Affairs in Neuroscience. This role focuses on leading medical strategies, overseeing evidence generation, and ensuring compliance with medical quality standards.

Medical Affairs to be a primary client contact. This role involves overseeing project management, ensuring high-quality deliverables on time and on budget, and leading teams to develop Medical Affairs strategies.

Biocomposites, located in Keele, UK, is hiring for a regulatory affairs development role aimed at providing strong grounding in regulatory matters. Enthusiastic individuals eager to learn and grow in the medical devices sector are encouraged to apply.

The Role**Our Medical Science Liaisons (MSLs) are field-based medical affairs professionals covering various countries or regions across Europe. This is an exciting opportunity to be part of the passionate, high-profile, high-impact Medical Affairs (MA) team, and work in a dynamic and collaborative

This position reports to the Senior Director, Medical & Scientific Affairs – Acute Care and is part of the Medical & Scientific Affairs organization, a team of medical specialists dedicated to all medical aspects of safe and effective diagnostics. MSL experience working in the medical technology,

The Senior Consultant, Medical Affairs Strategic Advisory is responsible for developing comprehensive intelligence, strategy, and impact measurement initiatives that support Medical Affairs objectives across the product lifecycle, with a strong emphasis on pre‑launch activities. Operating mainly i

You will oversee clinical trials, providing crucial medical input and training to project teams. Applicants should have 6–8 years of experience in the CRO or Pharma industry, demonstrating proficiency in medical monitoring and business development. Worldwide Clinical Trials in the United Kingdom i

Experience creating a range of medical affairs and medical education deliverables. Langland, a Publicis Health company, is the only health communications agency that thinks further across Clinical Trial Experience, Medical Strategy & Education, Public Relations & Policy, and Advertising, to create u

A leading medical device firm in the United Kingdom is seeking a skilled Regulatory Affairs Manager. This position requires a strong background in medical device regulatory affairs and the ability to ensure compliance and safety in healthcare innovation. In this role, you will lead the Regulatory Af

Lead the end-to-end delivery of a variety of medical affairs projects. Provide strategic input into service line growth, innovation, and operational effectiveness, identifying opportunities to evolve and strengthen our Medical Affairs offerings. Stay abreast of industry trends, best practices, and e

The role requires a medical degree and extensive medical affairs experience, focusing on strategic collaboration, scientific communication, and KOL engagement. A leading global biopharmaceutical company in London seeks a Global Medical Director for Migraine to drive product development and lifecycle

The role involves implementing medical affairs plans, managing a field medical team, and building relationships with key opinion leaders. Galderma is seeking a Medical Affairs Lead in Aesthetics based in London, UK. Candidates must have a medical degree or pharmacy qualification, alongside demonstra

Reporting to the Head of IQVIA Medical Communications, this role is accountable for the strategic growth and management of our flourishing Medical Affairs Communications practice, leading a team of 18 Account Handlers to achieve strong customer relationships, outstanding medical communications solut

This role involves ownership of Medical Grants, compliance, and operational excellence within Medical Affairs. Candidates should have over 10 years of experience in the pharma/biotech industry, with a focus on Medical Grants and Governance. A global biotech company in Greater London is seeking an ex

You will bring a high level of scientific/clinical knowledge as well as your strong business acumen to provide medical affairs strategy insights to our pharmaceutical and biotech customers.

A leading healthcare solutions provider in the United Kingdom is seeking a Medical Affairs Lead to oversee the planning and execution of Medical Affairs strategies.

The ideal candidate will have considerable experience in a medical communications agency, expertise in various therapy areas, and a proven track record of maintaining high editorial standards. A global health communications agency in London is seeking a Senior Medical Writer I to deliver scientific

A global biopharmaceutical solutions organization is seeking a Medical Affairs Lead specializing in Infectious Disease to manage healthcare projects.

Candidates should have substantial experience in medical communications and a strong understanding of various therapy areas. A leading health communications agency is seeking a Senior Medical Writer I to manage scientific content and mentor junior staff.