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Job Title: Quality Engineer II Location: Cambridge, UK Duration: 12 Months Work Type : Hybrid Overview: TekWissen is a global workforce management provider throughout the UK, Europe and many other countries in the world. The below client is an American multinational pharmaceutical and biotechnology corporation. Job Description: • This position is in the Biotherapeutics Pharmaceutical Research and Development Devices Centre of Excellence located in client location., • The incumbent will provide design control and risk management subject matter expertise to medical device and combination product development programmes throughout the product lifecycle., • This will involve generation and review of design history file and risk management file components whilst interacting with cross functional development teams at all levels of the organisation. POSITION RESPONSIBILITIES • Lead design control and risk management activities for combination product development programs, ensuring deliverables are appropriately authored, approved, and maintained to support clinical trials and commercial licensures., • Support and facilitation of effective risk management activities at external design companies and manufacturing facilities related to assigned projects., • Ensure combination product development activities are compliant with quality and regulatory standards, both internal and external., • Provide input and support to design validation including, but not limited to, human factors engineering assessments., • Support the assessment of external design companies and suppliers for capability of quality systems, facilities, and procedures to support device development and supply., • Support device design and manufacturing investigations from devices used in clinical trials and commercial manufacture., • Support the generation of all regulatory submission data and content for assigned device projects., • Support internal and external audits of the DCoE Quality Management System. EDUCATION, SKILLS AND EXPERIENCE • BSc in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 2 years of relevant experience in the pharmaceutical combination product and/or device industries, • OR MSc in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 2 years of relevant experience in the pharmaceutical combination product and/or device industries OR PhD in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline)., • History of working in accordance with the requirements of ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation., • Experience in design controls and risk management for combination products., • Familiar with Human Factors Engineering - Usability Engineering., • Familiar with device assembling manufacturing processes. TECHNICAL SKILLS REQUIREMENTS. • Working knowledge of ISO 9001, ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation., • Familiarity with EN 62366, EN 60601, and EN 62304., • Able to learn and apply established procedures in a reliable and consistent manner., • Capable of working independently with minimal supervision., • High level of attention to technical details and accuracy., • Able to prioritize multiple responsibilities and to work on multiple tasks simultaneously., • Able to work collaboratively in cross functional teams., • Excellent communication (e.g., oral, written, presentation) and interpersonal relationship skills., • Proficiency in general computer software such as word processing, spreadsheets, presentations., • Understand Good Manufacturing Practices (GMP). PHYSICAL POSITION REQUIREMENTS • Sitting, ability to travel TekWissen® Group is an equal opportunity employer supporting workforce diversity.

Job Title: Drug Discovery Oncology Project Leader (Biology) Location: United Kingdom (Hybrid/Flexible) Employment Type: Full-time About the Role We are looking for an experienced Drug Discovery Oncology Project Leader with a strong biology background to lead innovative oncology programmes from early target identification through to candidate selection. This role will play a critical part in shaping biological strategy, ensuring deep understanding of disease biology, mechanism of action and translational relevance across programmes. You will provide scientific leadership to multidisciplinary teams, acting as the biological authority within projects and driving robust, hypothesis-led decision-making. Key Responsibilities • Lead oncology drug discovery programmes with a primary focus on tumour biology, disease mechanisms and target validation, • Define and drive biological strategy, including mechanism of action, pathway biology and disease relevance, • Oversee design and interpretation of in vitro and in vivo biology studies, ensuring translational relevance, • Guide biomarker identification and translational biology strategies to support clinical progression, • Work closely with Medicinal Chemistry, DMPK, Safety and Translational teams to ensure biology-led optimisation, • Develop and manage integrated project plans, milestones and scientific risk mitigation, • Act as the scientific lead for biology in project governance and senior leadership discussions, • Ensure high scientific quality, data integrity and clear decision criteria across programmes, • PhD (or equivalent experience) in Cancer Biology, Molecular Biology, Cell Biology or a related discipline, • Extensive experience in oncology drug discovery biology within pharma or biotech, • Strong expertise in target identification, validation and disease modelling, • Experience with translational biology and biomarker strategy is highly desirable, • Proven ability to lead cross-functional teams and influence without direct authority, • Lead biology-driven oncology programmes with meaningful patient impact, • Influence scientific direction and portfolio strategy, • Collaborative, research-led culture with access to cutting-edge oncology platforms If you are passionate about cancer biology and driven to translate biological insight into transformative medicines, we would love to hear from you. Apply via LinkedIn or contact us for a confidential discussion.

Pharmacy Manager – Brand New State-of-the-Art Hospital £60,000 DOE + Competitive Company Benefits Cambridge - Cambridgeshire Full-Time/ Permanent - 40 Hours Want to be a key part in the opening and success of a BRAND NEW and state of the art hospital? Would you like to be able to build your own team from the ground up? Interested in developing your own department policies and procedures? Compass Associates are proud to have exclusively partnered with Welbeck Health Partners for the opening of their brand-new hospital, boasting 12 specialties equipped with the latest technology and world-renowned consultants dedicated to delivering the best patient experience. Capitalising on the success of their London flagship hospital, their new site will offer a wide range of medical diagnostic and same-day minimally invasive services, including heart health, lung health, digestive health, ENT, endoscopy, and neurology. This is a very exciting opportunity for an individual who wants to help to shape a growing, but established healthcare organisation. Welbeck Health Partners was founded by leading healthcare specialists from the UK and USA who shared a clear vision: to deliver better care and redefine what a healthcare organisation can be. Welbeck’s unique partnership model empowers clinicians to share in the success of the group while fostering a collaborative environment. It provides a framework for consistent patient pathways, quality assurance across partners, and smooth cross-referrals between specialties. Joining Welbeck means becoming part of a growing network of high-quality clinics and world-leading healthcare professionals. Welbeck are committed to creating a supportive, values-driven environment where their people can thrive. The company invests in its people, providing ongoing professional development, clear career progression, and the resources needed to excel. If you’re looking to be part of a purpose-led organisation that is shaping the future of healthcare while fostering a culture of respect, teamwork, and shared success, we’d love to hear from you. What is in it for you? • Paid for park and rid, • Great work-life balance, • Professional registration paid for annually, • Personal Development Plan, • 27 Days Annual Leave + Bank Holidays, • Private Medical Insurance, • Eye Care, • Annual Flu Vaccines, • Private Pension, • Season Ticket Loan / Cycle to Work Scheme, • Employee Assistance Programme, • AND a range of policies supporting health and wellbeing We are seeking an experienced Pharmacist or Pharmacy Technician to provide their pharmaceutical knowledge and managerial experience in ensuring the care of the patients at the hospital. The successful candidate will be responsible for supervising the procurement, preparation, dispensation & distribution of medicines to patients while providing an excellent standard of care through the medical management service. This role will be a senior managerial position, with the need for an individual who is able to showcase excellent attention to detail and an upholder of the highest standards. You will be ensuring the pharmacy department operates in a timely and consistent manner whilst overseeing the general running of the service, providing clinical input where necessary. Responsibilities: • Ensure full compliance with relevant legislation (e.g. GPhC, MHRA, CQC) and national guidance relating to medicines management., • Lead the quality assurance agenda to ensure compliance with all regulatory, legal and professional standards required for achieving and maintaining Home Office Licence and CQC compliance with conjunction with Superintendent Pharmacist., • Promote evidence-based, cost-effective prescribing and medicine management through collaboration with prescribers., • Ensure all possible measures are taken to safeguard the health, safety and wellbeing of patients by maintaining a high-quality and safe clinical environment., • Monitor and report medication incidents, lead root cause analysis (RCA) where necessary, and drive continuous improvement initiatives., • Localise the development, implementation, and review of policies and SOPs for safe handling, prescribing, dispensing, and storage of medicines., • Manage pharmacy staff, including pharmacists, technicians, and dispensers, ensuring effective rota coverage and workforce planning., • Ensure adequate training provision and compliance with identified clinical training requirements., • Provide guidance and support to staff, whilst fostering a culture of openness, psychological safety, and professional integrity where staff feel confident to speak up., • Provide mentorship and development opportunities for team members, including support with professional registration and revalidation, • Lead on recruitment, training, supervision, and performance management of the pharmacy team, • Ensure compliance with GPhC Code of Professional Conducts, Ethics Performance and their implications for practice., • Support medicines optimisation and initiatives including the implementation of electronic prescribing systems, • Manage the pharmacy budget, ensuring appropriate procurement, stock management and cost control of medicines and consumables, • Provide advice and support to consultants, healthcare professionals, centre colleagues and patients ensuring the safe, appropriate and cost-effective use of medicines What can you bring? • Registered pharmacist or pharmacy technician with a current GPhC registration and postgraduate qualification (Certificate), • Demonstrable management experience in a pharmacy and leadership within a clinical setting, • Knowledge of medicines legislation, governance frameworks, and clinical standards, • Knowledge of GPhC Code of Professional Conducts, Ethics Performance and their implications for practice, • Strong clinical knowledge in a healthcare setting, ideally with surgical experience, • Must have experience and the desire to develop new high-quality services, • Dispensary working experience and skills, • Working with IT systems and data analysis, • Experience of CQC inspections and/or readiness, • Be able to utilise your leadership skills to demonstrate and implement clinical best practice, • Ability to lead audits, investigations and quality improvement projects, • The successful candidate will be able to demonstrate excellence in:, • Leadership & people management skills within a multi-disciplinary team, • Adaptability and agility, • Communications skills - presenting, influencing, persuading and negotiating, • Collaboration – building partnerships and strategic working relationships, • Integrity and resilience, • Problem solving skills, • Planning, organisation and delegation skills. Recommendations We’re currently recruiting for a variety of management, clinical, and non-clinical roles across Oxford and Cambridge - if this role isn’t for you, but you would be interested in exploring roles feel free to share your details. If you know someone who may be interested in this or other roles in a new private hospital, we offer a £200 voucher referral reward for every successful recommendation.

Supplies Manager – Brand New State-of-the-Art Hospital £46,000 DOE + Competitive Company Benefits Cambridge Full-Time/ Permanent | Hybrid Want to be a key part in the opening and success of a BRAND NEW and state of the art hospital? Compass Associates are proud to have exclusively partnered with Welbeck Health Partners for the opening of their brand-new hospital, boasting 12 specialties equipped with the latest technology and world-renowned consultants dedicated to delivering the best patient experience. Capitalising on the success of their London flagship hospital, their new site will offer a wide range of medical diagnostic and same-day minimally invasive services, including heart health, lung health, digestive health, ENT, endoscopy, and neurology. This is a very exciting opportunity for an individual who wants to help to shape a growing, but established healthcare organisation. Welbeck Health Partners was founded by leading healthcare specialists from the UK and USA who shared a clear vision: to deliver better care and redefine what a healthcare organisation can be. Welbeck’s unique partnership model empowers clinicians to share in the success of the group while fostering a collaborative environment. It provides a framework for consistent patient pathways, quality assurance across partners, and smooth cross-referrals between specialties. Joining Welbeck means becoming part of a growing network of high-quality clinics and world-leading healthcare professionals. Welbeck are committed to creating a supportive, values-driven environment where their people can thrive. The company invests in its people, providing ongoing professional development, clear career progression, and the resources needed to excel. If you’re looking to be part of a purpose-led organisation that is shaping the future of healthcare while fostering a culture of respect, teamwork, and shared success, we’d love to hear from you. What is in it for you? • Paid for park and ride, • Great work-life balance, • Professional registration paid for annually, • Personal Development Plan, • 27 Days Annual Leave + Bank Holidays, • Private Medical Insurance, • Eye Care, • Annual Flu Vaccines, • Private Pension, • Season Ticket Loan / Cycle to Work Scheme, • Employee Assistance Programme, • AND a range of policies supporting health and wellbeing This managerial role offers an exciting opportunity for an accomplished and motivated Supplies Manager to lead the delivery of an efficient and effective supplies service within the Welbeck Regional Centre. You will play a central role in managing all aspects of stock management, supplier relationships, and inventory control to support clinical and non-clinical services across the Centre. The role encompasses leadership of the supplies team, operational performance management, procurement coordination, cost control, and ensuring compliance with regulatory, contractual, and organisational standards. We are seeking an individual who can embed best practice into everyday operations at the Welbeck site through close collaboration with clinical teams, senior leadership, and key stakeholders. You will be supported by the Operations Director and will work in partnership with the Procurement Team, Accounts Teams, and clinical and administrative leaders to continually enhance and develop supplies services. Responsibilities: • Leading the supplies team to ensure all departments have the right products in the right quantity, quality, place, and time to support clinical and non-clinical services., • Managing stock levels, stock location details, demand capture, distribution, and loan kit coordination in collaboration with CSSD and clinical teams., • Setting up and maintaining supplier relationships, including onboarding new suppliers, negotiating pricing, and monitoring compliance with service contracts., • Approving and managing invoices, coordinating with Accounts Payable and Accounts Receivable, and resolving discrepancies., • Costing new procedures in collaboration with clinical teams and monitoring net profit for existing procedures., • Developing, implementing, and maintaining standard operating procedures, training manuals, and systems for supplies management., • Ensuring effective operational performance, including monitoring, auditing, and reporting on supplies activity., • Contributing to continuous improvement initiatives, sustainability projects, and innovative procurement solutions., • Supporting recruitment, induction, performance management, and development of the supplies team to build a high-performing, collaborative culture., • Engaging with stakeholders across the Centre to optimise expenditure, streamline replenishment processes, and maintain uninterrupted service delivery., • Ensuring compliance with Health & Safety, infection prevention, safeguarding, confidentiality, and equality & diversity requirements. What can you bring? • Substantial experience in supplies, procurement, or inventory management, within a healthcare or multi-specialty environment., • Proven leadership and team management experience, with the ability to motivate and develop staff., • Strong organisational, planning, and analytical skills, including budget and cost control experience., • Experience in supplier management, contract negotiation, and service-level monitoring., • Knowledge of compliance and governance requirements within a healthcare setting., • Excellent interpersonal and communication skills to build strong relationships with internal teams, suppliers, and stakeholders., • Demonstrable commitment to quality, patient-centred service, and continuous improvement., • Proficiency with supplies management systems, ordering platforms, and data analysis tools. Recommendations We’re currently recruiting for a variety of management, clinical, and non-clinical roles across Oxford and Cambridge. If this role isn’t for you but you are interested in exploring other opportunities, feel free to share your details. If you know someone who may be interested in this or other roles in a new private hospital, we offer a £200 voucher referral reward for every successful recommendation.

Job Title - Quality Engineer Location – Cambridge Contract - 12 months Working pattern - Hybrid - Cambridge (2.5 days per week / 5 days per fortnight onsite) Salary - PAYE - £16.77 p/h up to £25.98 p/h, Umbrella - £18.79 p/h up to £29.12 p/h SRG are working with a global pharmaceutical company that are seeking a Quality Engineer to join their busy team. Key responsibilities: • Lead design control and risk management activities for combination product development programs, ensuring deliverables are appropriately authored, approved, and maintained to support clinical trials and commercial licensures., • Support and facilitation of effective risk management activities at external design companies and manufacturing facilities related to assigned projects., • Ensure combination product development activities are compliant with quality and regulatory standards, both internal and external., • Provide input and support to design validation including, but not limited to, human factors engineering assessments., • Support the assessment of external design companies and suppliers for capability of quality systems, facilities, and procedures to support device development and supply., • Support device design and manufacturing investigations from devices used in clinical trials and commercial manufacture., • Support the generation of all regulatory submission data and content for assigned device projects., • Support internal and external audits of the DCoE Quality Management System., • Identify, communicate, and develop strategies to improve combination product systems. Basic Qualifications: • BSc, MSc or PhD in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 2 years of relevant experience in the pharmaceutical combination product and/or device industries, • History of working in accordance with the requirements of ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation., • Experience in design controls for combination products., • Device risk management expertise., • Familiar with Human Factors Engineering - Usability Engineering., • Understand project management methodologies and capable to provide technical leadership for projects., • Familiar with device assembling manufacturing processes., • Thorough working knowledge of ISO 9001, ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation., • Working knowledge of EN 62366, EN 60601, and EN 62304., • Able to learn and apply established procedures in a reliable and consistent manner., • Capable of working independently with minimal supervision.

Experience in using AI tools for medical writing. Job Title: Director, Clinical Regulatory Writing. Are you ready to lead the charge in transforming breakthrough science into life-altering solutions? As the Director of Clinical Regulatory Writing, you'll be at the forefront of driving strategic comm

AJM Healthcare is a leading provider of wheelchair & community equipment services to the NHS and the Private Sector. Plan training sessions for internal staff and external healthcare professionals whilst co-ordinating a multi-disciplined team and manage projects when required. To be considered for t

A prestigious educational institution in Cambridge is seeking an Assistant/Associate Professor in Cardiology (Honorary Consultant) for a 5-year fixed-term role.You will lead and deliver a programme of cardiovascular research, while engaging in clinical duties and education.The ideal candidate is a q

Benefits include 25 days annual leave and a pension scheme, with a closing date for applications on 31st December 2025.

A leading pharmaceutical company in Cambridge is seeking a Director of Clinical Regulatory Writing to oversee the communication strategy for drug submissions.

A biopharmaceutical company in Cambridge is seeking a Medical Director to oversee clinical development activities from IND through Proof-of-Concept. The ideal candidate will lead clinical efforts for innovative treatments, provide medical direction, and ensure regulatory compliance.

Are you ready to lead the charge in transforming breakthrough science into life‑altering solutions? As the Director of Clinical Regulatory Writing, you’ll drive strategic communication excellence to achieve successful submissions and approvals. Continually develop best practices for the Clinical

Business Administration Manager – Nuffield Health Cambridge Hospital. As a Business Administration Manager at Cambridge Hospital, you will bring strong administrative experience, excellent organisational skills, commercial savvy and a passion for customer service. Manage and lead non‑clinical bu

You will work on a vibrant hospital campus with a friendly community feel; we have excellent facilities to practise your skills and abilities to support your career pathway and development. You will provide expert clinical skills to a very busy nurse practitioner role supporting the Benign Gynaecolo

A leading NHS hospital in Cambridge is searching for a Dementia Clinical Nurse Specialist to provide expert care for patients living with dementia.The successful candidate will lead initiatives and ensure compliance with care standards, acting as a resource for clinical teams.Strong communication an

A leading educational organization in the UK is seeking a Health Centre Manager to lead healthcare provision across multiple school sites. This senior, hands-on role involves overseeing clinical care, managing staff, and ensuring compliance with best practices. This is an opportunity to influence he

Hold lead responsibility for overseeing Divisional education provision for NMAHPs and Clinical Support Workers (CSWs). Experience of supporting education quality improvement activities in response to learner feedback. Sound awareness of cultural and learning diversity.

Our surgeries have a wide range of high quality equipment and materials ensuring that you have the clinical freedom to offer high quality standards of patient care. Lead clinician on hand to help discuss cases and patient issues and actively encourage this. We have a successful and robust internal m

Associate Director, Clinical Operations Lead. Associate Director, Clinical Operations Lead. Maintain up-to-date knowledge of the therapeutic area, product candidates, clinical practice, competitors, and regulatory requirements.

SRG is delighted to be working with a seed-stage biotech to help them find a Pre-Clinical Research Lead. Project leadership to build and maintain the integrated project plan (timeline, budget, risk log) for GLP tox, CMC, regulatory and clinical work-streams. The organisation is developing a non-vira

Job Title: Lead Clinical Research Associate. Join a highly experienced team dedicated to excellence in clinical research. Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent proper storage and accountability of clinical supplies and following-up of drug

Clinical Lead Case Manager - Brain/Spinal Injuries - Midlands. Compass Associates is excited to be working with a well-established and expanding business, to recruit a Clinical Manager for the Midlands region. Your working week will be split between holding a small clinical caseload and providing tr

Provide clinical leadership, mentoring, and guidance to colleagues across designated clinics. Strong leadership, mentoring, and communication skills. Audiological Science Ltd is a leading provider of audiology services, committed to improving the quality of life for our patients.

As part of a multi-disciplinary team, and in alignment with Optegra values, ensure a comprehensive level of care provision to all ophthalmic patients, their relatives, or carers, across clinical and non-clinical care pathways, with an emphasis on quality patient care across all hospitals within the

Were proud of our happy home and are dedicated to creating a place where everyone enjoys coming to work each day.As well being part of a lively and supportive team, we are surrounded by fascinating residents who also bring so much to our lives every day too.Full time - 40 hours per week (Supernumera

With career progression opportunities into senior clinical and commercial leadership, this is a fantastic opportunity to grow your career. This hybrid role combines clinical expertise with business development, perfect for those with tracheostomy and ventilation skills and a knack for package develo

As a Complex Care Clinical Lead, you will: Lead and manage complex care packages for adults, paediatrics, and those with learning disabilities or mental health needs Develop and secure new care packages from ICBs, commissioners, case managers, and private clients Represent the company clinically du

Director Clinical Operations Lead.

Why join us?Were proud of our happy home and are dedicated to creating a place where everyone enjoys coming to work each day.As well being part of a lively and supportive team, we are surrounded by fascinating residents who also bring so much to our lives every day too.Benefits of

Provide clinical leadership and mentorship to Oncology Early Clinical Development Medical Directors and Clinical Scientists. This leadership role bridges preclinical research and clinical development to ensure innovative therapies transition from lab to clinic. Executive Director, Oncology Early Cli

A global biopharmaceutical company is seeking a Director, Clinical Trial Start-Up to lead the strategic direction and operational oversight of the Study Start-Up process. This role requires excellent leadership capabilities to enhance team performance and ensure regulatory compliance across clinical

Care Team Clinical Lead - Temporary Full-time page is loaded## Care Team Clinical Lead - Temporary Full-timelocations: Durham Region, ONtime type: Full timeposted on: Posted 3 Days Agojob requisition id: JR202501462VHA Home HealthCare (VHA) is one of the largest not-for-profit home care prov

The Clinical Lead is consideredthe expert and will take ownership for the operational delivery of the clinicalservice in the Centre of Excellence and Innovation; with an ability to take apopulation health view rather than a pure individual focus. The Clinical Lead for the Lymphoedema Team will manag

Have held a clinical leadership role and can demonstrate managing others. Are you a passionate and caring Registered Nurse looking for a rewarding career with excellent training and opportunities for development? Join Care UK as Clinical Lead and we will give you all the support and training you nee

A leading hospice care provider in the UK is seeking a compassionate Clinical Lead to oversee the clinical aspects of their hospice care program.

Under the strategic leadership of the MIDD Head, the MIDD team drives strategy and innovation in clinical pharmacology and quantitative medicine. Collaboration is central to this role, requiring close partnership with AI/ML lead & experts within the MIDD team, Clinical Pharmacology Modelling & Simul

The MIDD Lead is a scientific and strategic leader who applies modelling and simulation to inform drug development decisions. The MIDD Lead is responsible for leading the development and implementation of MIDD evidence strategies, serving as an advanced technical and subject‑matter expert for a th

A leading drug development company in the United Kingdom is seeking an experienced Associate Principal Regulatory Writer. The role involves leading regulatory document strategies, managing project budgets, and collaborating with teams to ensure high-quality submissions.

The ideal candidate will have over 4 years of experience navigating EU regulatory requirements, especially Clinical Trial Applications.

Ensure clinical leadership, advice, and support are readily available to the County Commissioner and colleagues. Oversee clinical operations and community delivery. Conduct regular audits to monitor and assure the quality of clinical activities.

Deputise for the Service Manager when required, ensuring continuous leadership and clinical oversight. Our new 12‑14 bed CQC‑registered service will provide specialist, clinically‑led community rehabilitation for people with complex mental health needs, delivering 24/7 clinical support in a sa

A healthcare organization in London is seeking a Clinical Lead for Lymphoedema to oversee clinical service delivery and lead a dedicated team. The successful candidate will collaborate closely with the Director of Clinical Services to ensure high-quality patient care and effective resource managemen

A global business and technology transformation leader is seeking a Senior Consultant in Life Sciences to support growth in early R&D and clinical projects. You will lead initiatives that deliver data-driven insights and strategic recommendations tailored for pharmaceutical clients.

A leading clinical research organization in the UK is seeking a Regulatory Manager / Senior Regulatory Manager. The role focuses on providing regulatory strategy and guidance for clinical trials, ensuring compliance with applicable regulations, and preparing high-quality regulatory submissions.

A leading biopharma company in Greater London seeks a Clinical Development Medical Director to provide insights and leadership in clinical studies focused on vascular pathology. Candidates must hold a medical degree and have experience in clinical research, with preferred qualifications in board cer

A leading company is seeking a Clinical Lead GP near York to provide clinical leadership in a medium-sized teaching practice. The role involves managing a team of GPs and clinical support staff in a modern health center while ensuring a manageable workload with rare home visits.

A leading biopharmaceutical company based in the United Kingdom is seeking a Head of Medical Science to shape their scientific vision and medical strategy. The ideal candidate will possess over 10 years of experience in drug development, particularly in CNS/Neuroscience, and will excel in leading mu

A leading healthcare solutions provider is looking for a Category Manager (Clinical) in London to oversee a category with an annual spend of £10-£20 million. In this role, you will lead strategic sourcing initiatives, develop robust supplier relationships, and negotiate high-value contracts to ach