Company Detail

Job Openings

• 

  QA Scientist Analyst  

  Proclinical

  [fulltime] - Worthing

  Posted: 21/01/2026

  Apply Now

  Help bring science to life and join a leading pharmaceutical company t... Read More

  Help bring science to life and join a leading pharmaceutical company to play a key role in delivering impactful research that drives healthcare innovation!Proclinical is seeking a QA Scientist Analyst to join the QA Technical Support Team in Worthing. In this role, you will provide analytical technical support to QA and site operations, contributing to investigations, plant trials, validation activities, and non-routine testing. This position requires adherence to cGxP standards and ensures the site's analytical capabilities are maintained. Responsibilities:Provide analytical technical support to QA and site operations.Investigate issues related to analytical methods and instrumentation.Support plant trials and validation activities.Conduct non-routine analytical testing as needed.Prepare, interpret, and present technical reports.Perform additional duties as directed by the QA Technical Support Team Leader.Key Skills and Requirements:Experience working under cGxP standards.Background in a pharmaceutical GMP environment such as QA, Development, or R&D.Practical experience with chromatography, spectroscopy, electrochemical techniques, and physical testing techniques.Strong planning, organizational, and time management skills.Ability to make decisions, solve problems, negotiate, influence, and communicate effectively.Strong interpersonal skills for effective collaboration with teams and contractors.Proficiency in IT systems.Well-developed verbal, written, numerical, and presentation skills.
  Read Less

  Apply Now
• 

  Senior Principal Scientist In Vivo Pharmacology  

  Proclinical

  [permanent] - Nottingham

  Posted: 20/01/2026

  Apply Now

  Are you looking to drive groundbreaking medical research and make a re... Read More

  Are you looking to drive groundbreaking medical research and make a real impact? Join our client and lead the way in advancing In Vivo Pharmacology!Proclinical is seeking an experienced and dedicated Senior Principal Scientist with expertise in metabolic disorders to focus on scientific leadership, driving innovative research, and collaborating with internal teams and clients to advance drug discovery projects. The position is fully onsite and offers the opportunity to contribute significantly to the progression of science. Responsibilities:Lead and oversee in vivo pharmacology and drug discovery programs.Mentor and guide team members while fostering innovation in experimental and technological approaches.Act as a Project Lead, coordinating the delivery of high-quality scientific outcomes.Collaborate with internal teams and clients to design and execute complex drug discovery projects.Address scientific and technical challenges with innovative problem-solving skills.Ensure compliance with UK/European legislation governing in vivo research and oversee experimental designs.Key Skills and Requirements:Advanced degree or equivalent experience in a relevant field alongside a strong background in drug discovery.Expert knowledge in metabolic diseases such as obesity, diabetes, and cardiometabolic conditions, with hands-on experience in in vivo pharmacological research methods.Deep knowledge of the drug discovery process and current therapeutic landscape.Familiarity with UK/European regulations for in vivo research and experience in designing and overseeing studies.Expertise in designing and setting up of In Vivo model studies supporting drug discovery programs Proven ability to work effectively in a fast-paced, collaborative environment.Strong organizational and data management skills, with the ability to manage multiple projects simultaneously. Read Less

  Apply Now
• 

  Associate Director, Clinical QA (GCP)  

  Proclinical

  [permanent] - London

  Posted: 16/01/2026

  Apply Now

  Are you driven by improving oncology outcomes and looking for a role w... Read More

  Are you driven by improving oncology outcomes and looking for a role where quality truly matters? Looking for a flexible position where you can work from the comfort of your home?Proclinical is seeking an Associate Director of Clinical Quality Assurance to support clinical programs and trials with a focus on Good Clinical Practice (GCP) compliance. This role involves ensuring the highest quality standards in clinical trial documentation, addressing quality issues, and preparing for regulatory inspections.Responsibilities:Review key clinical trial documentation, including protocols, investigator brochures, informed consent forms, and trial master files.Lead assessments and investigations of quality issues, driving root cause analysis, remediation, and timely resolution.Facilitate reviews of potential serious breaches and urgent safety measures for assigned clinical programs.Coordinate GCP-GVP vendor audits, manage audit programs, and ensure proper execution and closure of audits.Oversee quality management with functional lines and vendors, including leading Quality Oversight Committee meetings.Collaborate on implementing risk-based quality management (RBQM) for studies, focusing on critical data identification and reporting.Lead pre-approval and routine regulatory inspection readiness activities, including strategy development and program management.Provide guidance and training on compliance issues, leveraging expertise in GCP and industry best practices.Support the development, implementation, and maintenance of GCP standard operating procedures (SOPs).Key Skills and Requirements:Strong background in clinical quality assurance and GCP compliance.Experience in reviewing and managing clinical trial documentation.Knowledge of regulatory requirements and inspection readiness processes.Ability to lead audits and manage CAPAs effectively.Familiarity with oncology clinical trials is preferred.Excellent problem-solving skills and adaptability.Strong collaboration and communication abilities.
  Read Less

  Apply Now
• 

  European Marketing Director  

  Proclinical

  [fulltime] - London

  Posted: 16/01/2026

  Apply Now

  Looking for a new challenge where you can lead bold strategies? Our cl... Read More

  Looking for a new challenge where you can lead bold strategies? Our client is looking for a marketing director to amplify innovation and cutting-edge biotech solutions at the forefront of global healthcare.Proclinical is seeking a Marketing Director for Europe to lead and develop marketing strategies within the oncology space. This role focuses on brand planning, market research, and executing global marketing strategies tailored to the European market. You will collaborate with cross-functional teams, manage product launches, and ensure compliance with industry regulations. This position requires a strategic thinker who can adapt global initiatives to local needs while driving impactful results. Responsibilities:Develop and execute European brand plans in alignment with global strategies.Conduct market research and competitive analysis to inform forecasting, positioning, and messaging.Adapt and implement global marketing strategies for the European market.Collaborate with cross-functional teams, including market access, sales, medical, and regulatory.Design and deploy disease state education campaigns.Manage product launches and promotional campaigns.Create and oversee marketing materials and digital content.Plan and execute congress presence and promotional activities in collaboration with global marketing.Ensure compliance with industry regulations and company policies.Implement sales infrastructure, including CRM systems and KPI tracking platforms.Monitor campaign performance and report on ROI.Manage marketing budgets and allocate resources effectively.Identify new market opportunities and customer segments.Support field teams with tools and training materials.Establish clear engagement plans and roadmaps.Key Skills and Requirements:Bachelor's degree in a relevant field.Experience in oncology and pharmaceutical marketing roles.Strong ability to build and maintain professional relationships.Excellent communication skills, with the ability to simplify complex scientific information.Hands-on experience with product communications and evolving marketing channels.Strategic thinker with strong prioritization and project management skills.Business acumen and understanding of regulatory requirements in marketing.Leadership skills to influence and collaborate effectively with senior leaders.Initiative-driven, adaptable, and comfortable with ambiguity.Strong negotiation and conflict resolution skills.Team player with excellent organizational, presentation, and written communication skills.Solution-oriented with ethical judgment and quick decision-making abilities.Open to driving and supporting change.Ability to gather diverse input to drive innovative solutions. Read Less

  Apply Now
• 

  Technical Project Manager  

  Proclinical

  [permanent] - Taunton

  Posted: 14/01/2026

  Apply Now

  Lead breakthrough medical device innovations from concept to commercia... Read More

  Lead breakthrough medical device innovations from concept to commercialization with precision, purpose, and cross‑functional excellence.Proclinical is seeking a Technical Project Manager to lead innovative medical device development projects from concept to commercialization. This role focuses on disciplined project execution, ensuring alignment with business objectives and compliance with quality and regulatory standards. You will work in a collaborative environment, driving project success through effective planning, communication, and stakeholder engagement. Responsibilities:Develop and maintain detailed project plans, ensuring timely achievement of milestones.Utilize project management tools like Gantt charts and software (e.g., Smartsheet, MS Project) to track progress and dependencies.Communicate effectively with project teams, stakeholders, and leadership, providing clear updates and facilitating decision-making.Identify, assess, and mitigate project risks while managing budgets and expenditures (OPEX/CAPEX).Ensure compliance with medical device quality and regulatory requirements (e.g., ISO 13485) and internal Quality Management System procedures.Support continuous improvement initiatives, including lessons learned workshops and process enhancements.Build and lead cross-functional project teams, fostering collaboration and alignment with business goals.Key Skills and Requirements:Strong understanding of project management principles, methodologies, and tools.Experience in budgeting, cost control, and resource allocation for technical projects.Technical foundation in engineering or science with analytical skills and the ability to grasp new concepts.Familiarity with product development lifecycles, particularly in regulated industries like medical devices.Knowledge of quality management systems, risk management, and good documentation practices.Proficiency in project management software (e.g., Smartsheet, MS Project) and office productivity tools (Excel, PowerPoint, Word, Teams, Outlook).Strong leadership, communication, and stakeholder engagement skills.Ability to manage competing priorities, mitigate risks, and resolve complex project issues.Formal project management qualification (e.g., PMP, PRINCE2) and experience with Agile or Scrum methodologies are advantageous. Read Less

  Apply Now
• 

  Associate Director, Clinical QA (GCP) (Hybrid)  

  Proclinical

  [permanent] - Hertfordshire

  Posted: 07/01/2026

  Apply Now

  Lead the charge in safeguarding clinical excellence-step into a pivota... Read More

  Lead the charge in safeguarding clinical excellence-step into a pivotal Senior Director QA role where your expertise ensures the highest standards in pharmaceutical innovation.Proclinical is seeking an Associate Director of Clinical Quality Assurance to oversee GCP activities, lead audits and inspection management, and ensure the high-quality execution of clinical trials. This role involves collaborating with internal and external stakeholders, providing GCP QA support, and contributing to the continuous improvement of clinical development processes. Responsibilities:Represent Clinical Quality Assurance (CQA) in cross-functional team meetings.Support the training and development of CQA colleagues.Provide proactive GCP QA support to ensure patient safety, data integrity, and operational excellence.Conduct various audits, including Clinical Investigator Site Audits, GCP Document Audits, Clinical Study Reports, Trial Master Files, internal Process Audits, and Vendor-System audits.Act as the CQA Lead for clinical studies, managing audit plans and reports.Facilitate quality improvement by communicating audit results, CAPAs, and providing GCP guidance to clinical teams.Manage health authority inspection preparation and provide leadership during inspections.Review and provide input on clinical documentation such as protocols, study reports, IBs, and ICFs.Compile and analyze audit metrics to identify trends and communicate findings to business groups.Conduct GCP training sessions for internal teams.Key Skills and Requirements:Bachelor's degree in a relevant discipline.Experience in Clinical Quality Assurance within the pharmaceutical industry.Knowledge of health authority inspection management.Ability to develop SOPs and training materials.Proficiency in conducting routine, complex, and for-cause GCP audits.Strong interpersonal and professional communication skills.Effective time management and ability to handle competing priorities.Familiarity with US, EU, and international regulatory standards for clinical trials.Attention to detail, analytical thinking, and strong report writing skills.Ability to navigate challenging situations diplomatically and collaboratively.Proficiency in English (spoken and written).Willingness to travel approximately 25%.
  Read Less

  Apply Now
• 

  Supply Chain Planner & Senior Supply Chain Planner (2 Roles)  

  Proclinical

  [permanent] - Surrey

  Posted: 13/12/2025

  Apply Now

  Keep life-saving medicines moving-join us as a Supply Chain Planner an... Read More

  Keep life-saving medicines moving-join us as a Supply Chain Planner and make seamless delivery your mission.Proclinical is seeking a Supply Chain Planner and a Senior Supply Chain Planner for permanent roles based in Surrey. These positions focus on ensuring the seamless availability of pharmaceutical products to patients, avoiding stock-outs, and maintaining strong collaboration across various stakeholders, including commercial, regulatory, and manufacturing teamsResponsibilities:Plan and coordinate the replenishment of finished goods to distribution centers and third-party partners.Monitor stock levels to minimize write-offs due to expiration and initiate redistribution activities when necessary.Manage relationships with Contract Manufacturing Organizations (CMOs) to ensure effective collaboration.Organize and oversee shipments, including customs documentation and quality release processes.Conduct multi-site, multi-market, and multi-level planning to align supply with market demand.Analyze market forecasts, address deviations, and collaborate with commercial teams to define annual quantities and rolling forecasts.Ensure accurate and timely execution of supply chain activities in SAP, maintaining compliance with Good Distribution Practices (GDP).Oversee logistics operations, adhering to GDP, Quality Management Systems (QMS), and compliance programs.Raise and manage change controls and deviations, ensuring procedural adherence.Support the development and implementation of Standard Operating Procedures (SOPs) and performance scorecards for CMOs.Act as a team lead in the absence of the line manager.Key Skills and Requirements:Experience in the pharmaceutical or FMCG industry, particularly in forecasting, planning, and inventory management.Strong analytical, numerical, and data-driven approach.Proven ability to manage supplier relationships and negotiate effectively.Proficiency in GDP and GMP standards.Effective communication and stakeholder management skills.Familiarity with SAP ByDesign and strong MS Office skills.Agile thinker with problem-solving capabilities and a growth mindset.Demonstrated integrity, ethical standards, and collaborative teamwork. Read Less

  Apply Now
• 

  UK_European Tax Manager  

  Proclinical

  [fulltime] - Chester

  Posted: 09/12/2025

  Apply Now

  Drive tax strategy and compliance across Europe-join as a UK & Europea... Read More

  Drive tax strategy and compliance across Europe-join as a UK & European Tax Manager and make an impact at the heart of a global tax center of excellence. Proclinical is seeking a UK_European Tax Manager to join our client's team in Chester. This role is integral to the European Tax Center of Excellence, focusing on managing direct tax reporting compliance for various markets within Europe. You will also provide expert tax advice, working closely with external advisers and the Global Corporate Tax Department. A key part of your role will be staying informed about local tax legislation to effectively consult with stakeholders.Responsibilities:Prepare and submit US Tax reports, including quarterly tax provisions and projections using TaxStream technology.Coordinate annual Transfer Pricing documentation, analyzing financial data and liaising with commercial teams and external advisers.Collaborate with external advisers to prepare annual Corporate Income Tax Returns and calculate tax payments.Communicate with tax authorities as needed.Prepare annual tax disclosures for Statutory Financial Statements and address external auditor queries.Continuously review tax legislation, analyze impacts, and communicate changes to business partners.Participate in internal projects to ensure tax compliance and provide advisory support.Support the strategy for third-party resource use, ensuring proper engagement and approval.Contribute to standardization, automation, continuous improvement, and risk management strategies, leveraging tax technology developments.Provide support to other markets as required.Complete additional reporting requirements as necessary.Key Skills and Requirements:Qualified Accountant and/or Chartered Tax Adviser.Experience in tax compliance within a practice or multinational corporate tax environment.Understanding of accounting provisions, principles, statutory audit, and disclosure requirements in at least one European jurisdiction.Experience with indirect taxes is desirable.Fluency in English. Read Less

  Apply Now
• 

  Director, Global Evidence Generation - Immunology  

  Proclinical

  [permanent] - London

  Posted: 09/12/2025

  Apply Now

  Help bring science to life and join a leading pharmaceutical company t... Read More

  Help bring science to life and join a leading pharmaceutical company to play a key role in delivering impactful research that drives healthcare innovation!Proclinical is recruiting for a Director of Global Evidence Generation to oversee the design and implementation of strategic evidence generation initiatives for key assets in Immunology and Respiratory. In this role, you will collaborate with cross-functional teams to align on priorities, coordinate tactics, and ensure impactful delivery of evidence generation activities. This is an exciting opportunity to contribute to innovative therapies in a dynamic and collaborative environment. Responsibilities:Oversee the creation and implementation of the Integrated Strategic Evidence Generation plan in alignment with asset strategies.Provide strategic oversight on evidence generation needs, priorities, and tactics.Lead cross-functional collaboration to deliver cohesive evidence generation activities.Ensure timely execution of studies that support strategic goals and maximize impact.Manage budgets and track performance using key metrics and KPIs.Identify and establish external partnerships to enhance evidence generation efforts.Contribute to life-cycle management strategies for assigned assets.Key Skills and Requirements:Advanced degree in a medical or scientific field.Expertise in Immunology or Respiratory therapeutic areas is preferred.Working history in developing and executing global evidence generation strategies.Strong skills in data interpretation, communication, and building strategic partnerships.Familiarity with Real-World Evidence (RWE) and/or Health Economics and Outcomes Research (HEOR) is highly desirable.
  Read Less

  Apply Now

Load more jobs