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Executive Director Clinical Research - Permanent Position.

CK Group are recruiting for a Senior Outcomes Research Scientist to join a company in the pharmaceutical industry on a contract basis for 9 months, working hybrid in Welwyn Garden city. Salary: Per Hour: 55.96- 67.16 PAYE or 75- 90 Ltd/ Umbrella this role is outside IR35 Senior Outcomes Research Scientist Role: • Development, strategic & implementation of patient-centered fit-for purpose measurement strategies throughout the drug development lifecycle., • Collaborating with data science experts on study start-up, monitoring & close out., • Assess the need to develop, evaluate, & deploy new measurement tools to best capture the patient experience, • Provide subject matter expertise areas of clinical trial delivery such as measurement/digital strategy, linguistic validation, eCOA, site & patient engagement related to COAs. Your Background: • An MSc in Public Health, Psychology, or a related area (PhD preferred), or equivalent experience., • Previous hands-on experience in developing & implementing patient-centered measurement strategies, & in the planning, & dissemination of patient-centered evidence., • Previous experience within a pharmaceutical experience., • Direct experience in neuromuscular diseases or a strong interest in working in this area/ Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Location: This role is hybrid, working 2 days a week on site in Welwyn Garden City. Apply: For more information, or to apply for this Senior Outcomes Research Scientist please contact the Key Accounts Team onor email Please quote reference 147 056. It is essential that applicants hold entitlement to work in the UK Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. INDKA Employment Type : 4 Experience: years Vacancy: 1 Hourly Salary Salary: £ 55 - 90

Work closely with study teams and global partners to integrate meaningful patient feedback into research plans. Step into a senior-level contract position where you'll help shape how patient experiences are captured and understood in clinical research.

Location: Hatfield, Hertfordshire, UK Position Type: Full-time Seniority: Senior Scientist / Principal Scientist (based on experience) Salary: Competitive, dependent on experience ⸻ About Pharmidex: Pharmidex is a respected, science-led preclinical CRO, supporting global biotech and pharmaceutical clients in drug discovery and development. Pharmidex team have contributed to more than 15 drugs at different stages of clinical development. With an expanding portfolio across Respiratory, Oncology, and Infectious diseases, we are growing our preclinical team to meet increasing demand for high-quality, translational studies. This is an exciting opportunity for a motivated Senior or Principal Scientist to lead the establishment and execution of innovative translational preclinical models, contribute to client success, and shape the future of preclinical research at Pharmidex. ⸻ Key Responsibilities: • Take a lead role in establishing, developing, and validating preclinical models in-house – with a focus on respiratory disease, oncology, and infection., • Serve as Study Director, managing studies from planning and execution through to data reporting and scientific interpretation., • Coordinate and maintain a safe, compliant, and well-organised laboratory environment., • Support and supervise technical staff across all preclinical projects., • Engage with clients and collaborators to ensure successful delivery of studies and ongoing relationships., • Contribute to internal project reviews, innovation initiatives, and cross-functional discussions. ⸻ Your Background: • Degree (BSc/MSc/PhD) in Biological Sciences, Pharmacology, or a related life sciences discipline., • Minimum 3 - 5 years of hands-on preclinical experience in a pharma, biotech, or academic translational research setting., • Demonstrable experience in developing and running preclinical Respiratory or Oncology models., • Hold or have previously held a Home Office Personal Licence (PIL Modules 1–3 or equivalent)., • Proven ability to work in multi-disciplinary teams and independently manage projects., • Familiarity with preclinical techniques including multiple administration routes., • Competent in data analysis using GraphPad Prism, SPSS, or similar software., • Experience of managing large and complex studies with good documentation and planning skills., • Flexible and willing to conduct occasional out-of-hours work to meet study needs. ⸻ Desirable (not essential): • Experience with preclinical imaging techniques (e.g. IVIS, microCT)., • Practical expertise in cell culture or ex-vivo sample analysis., • Background in GLP or regulatory-aligned studies., • Previous exposure to client-facing roles or project oversight in a CRO setting. ⸻ Why Join Pharmidex? • Opportunity to work on diverse and impactful preclinical studies., • Be part of a growing team where your expertise will help shape model development and client delivery., • Flexible and collaborative culture with exposure to cross-disciplinary science., • Career development aligned with company growth. ⸻ What We Offer: • Competitive salary based on experience, • Defined career development path with mentorship and training support, • Company pension scheme with employer contribution, • Life insurance (4x annual salary), • Employee perks and discounts platform, • Free onsite parking and subsidised staff canteen, • Opportunities to volunteer and contribute to social impact projects Salary: Depending on experience Application Deadline: 04 August 2025 How to Apply: If you are passionate about translational science and ready to make an impact in improving patients lives please send your CV and a short cover note to

Proven CRA Expertise: Minimum of 2-4 years of experience as a Clinical Research Associate, demonstrating a strong understanding of clinical trial processes and a track record of successful site monitoring. Top-5 Pharma Hybrid CLINICAL RESEARCH ASSOCIATE - Accelerate Innovation & Shape the Future of

Join a highly experienced team dedicated to excellence in clinical research. As one of the few rapidly growing Contract Research Organizations (CROs) for UK studies, our client is expanding their site management team with multiple hires this year. They are involved in a diverse range of studies, inc

Join a highly experienced team dedicated to excellence in clinical research. As one of the few rapidly growing Contract Research Organizations (CROs) for UK studies, our client is expanding their site management team with multiple hires this year. They are involved in a diverse range of studies, inc

Job Title: Lead Clinical Research Associate. Join a highly experienced team dedicated to excellence in clinical research. Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;.

Senior Clinical Research Associate (SCRA). Contract Research Organization (CRO).

Senior Clinical Research Associate (SCRA). Contract Research Organization (CRO).

Join a highly experienced team dedicated to excellence in clinical research. Job Title: Lead Clinical Research Associate. They are involved in a diverse range of studies, including cutting-edge research in advanced therapies such as CAR-T.

We are seeking a motivated and detail-oriented Freelance Clinical Research Associate (Associate Level) with a passion for oncology clinical trials. Freelance Clinical Research Associate – Associate Level (Oncology). Minimum of 1–2 years of clinical research experience (internships or study coord

As a Clinical Research Physician, you will play a crucial role in the development and execution of clinical research studies. Experience in clinical research and drug development. Become part of our mission to advance clinical research and transform healthcare worldwide.

Proven CRA Expertise: Minimum of 2-4 years of experience as a Clinical Research Associate, demonstrating a strong understanding of clinical trial processes and a track record of successful site monitoring. Top-5 Pharma Hybrid CLINICAL RESEARCH ASSOCIATE - Accelerate Innovation & Shape the Future of

Clinical Research Associate (CRA) – Part-Time Consultant / Contractor. We are seeking an experienced Clinical Research Associate (CRA) level consultant to provide supplemental on-site and remote oversight in addition to CRO monitoring activities. Strong working knowledge of ICH GCP, clinical trial

Senior Clinical Research Associate – England. We are seeking an experienced Senior Clinical Research Associate (Senior CRA) to join a dedicated single-sponsor team in England. As a Senior CRA, you will be a key contributor to the successful delivery of clinical trials across England.

CRA #ClinicalResearch #ClinicalResearchAssociate #SeniorCRA #CRAJobs #PharmaJobs #FSP #LifeSciences #Hiring #ClinicalTrials #UKJobs#CCS-Global. We have an exciting, exclusive opportunity for an experienced Clinical Research Associate to join our clients newly established FSP team, working exclusivel

Clinical Research Associate II / UK Based / France / Belgium. Proven ability to manage 10–15 clinical study sites from start-up to close-out. Proficient in Microsoft Office and clinical trial systems (e.