The field of clinical research offers diverse opportunities for professionals interested in advancing healthcare. Clinical research jobs involve conducting studies to evaluate the safety and effectiveness of new treatments, therapies, and diagnostic tools. These roles are crucial for bringing innovative medical solutions to patients.1,542 Clinical Research jobs in the United Kingdom
Clinical Trial Manager
London, London
TFS HealthScience
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Job Description
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. About this role We're looking for a Clinical Trial Manager with experience in opthalmology clinical trials to join our FSP team , supporting a biotechnology company. You'll lead complex studies and help advance treatments that make a real difference for patients. Responsibilities Oversee trial execution (start-up to closeout) Manage CROs, vendors, and site relationships Support protocol and consent development Ensure regulatory compliance (ICH-GCP, FDA, etc.) Track budgets, timelines, and quality metrics Help prepare for audits and submissions Requirements 1–3 years in clinical trial/project management (biotech, CRO, or pharma) Degree in life sciences or related field Strong communication, problem-solving, and organizational skills Familiarity with global trial regulations and study phases Bonus: Ophthalmology experience What We Offer We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients A Bit More About Us Our journey began over 25 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients’ safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East. Our core values of Trust, Quality, Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization. Together we make a difference41bf1e1f-b16b-4260-a40a-17c77a06fd15
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Clinical Research Scientist
L2 5QS Liverpool, North West
£45000 Annually
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Our client is seeking a highly motivated and experienced Clinical Research Scientist to join their innovative pharmaceutical team based in Liverpool, Merseyside, UK . This role is critical in advancing drug development pipelines through rigorous scientific investigation and analysis. You will be responsible for designing, executing, and interpreting complex preclinical and clinical research studies, contributing to the development of novel therapeutic agents. Your duties will include developing research protocols, managing laboratory operations, ensuring adherence to Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) guidelines, and meticulously documenting all research activities. You will work collaboratively with cross-functional teams, including R&D, regulatory affairs, and clinical operations, to ensure seamless project progression. A key responsibility will be the analysis of research data, including statistical interpretation, and the preparation of comprehensive reports for internal review and regulatory submissions. You will also be expected to stay abreast of the latest scientific literature and technological advancements in pharmaceutical research and development. Presenting findings at scientific conferences and contributing to the publication of research in peer-reviewed journals will be an integral part of your role. The ideal candidate will possess a PhD or a Master's degree in a relevant scientific discipline (e.g., pharmacology, biochemistry, molecular biology) with a proven track record in pharmaceutical research. Excellent analytical, problem-solving, and critical thinking skills are essential, along with strong written and verbal communication abilities. Experience with statistical analysis software and relevant laboratory techniques is required. This is an exciting opportunity to contribute to life-changing medicines in a fast-paced, research-driven environment. The position is based at our client's state-of-the-art facility and requires full-time commitment on-site to leverage the advanced laboratory infrastructure and foster close collaboration within the scientific community.
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Clinical Research Scientist
B1 1BB Birmingham, West Midlands
£55000 Annually
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Our client, a leading pharmaceutical innovator, is seeking an experienced Clinical Research Scientist to join their dynamic, fully remote team. This role is crucial in advancing groundbreaking research and development projects aimed at bringing novel therapies to market. The successful candidate will play an integral part in the design, execution, and analysis of clinical trials, from early-phase studies to late-stage investigations. You will be responsible for developing study protocols, selecting investigational sites, and overseeing the conduct of trials to ensure adherence to scientific and ethical standards, as well as regulatory requirements.
Your responsibilities will extend to data interpretation, report generation, and contributing to scientific publications and regulatory submissions. This position requires a rigorous scientific approach, excellent analytical skills, and the ability to work independently and collaboratively within a virtual setting. You will liaise with cross-functional teams, including medical affairs, regulatory affairs, and manufacturing, to ensure seamless project progression. A strong understanding of Good Clinical Practice (GCP) and relevant regulatory frameworks (e.g., FDA, EMA) is essential. This is an exceptional opportunity to contribute to life-changing medicines and advance your career in a supportive and forward-thinking virtual environment.
Responsibilities:
Your responsibilities will extend to data interpretation, report generation, and contributing to scientific publications and regulatory submissions. This position requires a rigorous scientific approach, excellent analytical skills, and the ability to work independently and collaboratively within a virtual setting. You will liaise with cross-functional teams, including medical affairs, regulatory affairs, and manufacturing, to ensure seamless project progression. A strong understanding of Good Clinical Practice (GCP) and relevant regulatory frameworks (e.g., FDA, EMA) is essential. This is an exceptional opportunity to contribute to life-changing medicines and advance your career in a supportive and forward-thinking virtual environment.
Responsibilities:
- Design, develop, and manage clinical trial protocols.
- Oversee the execution of clinical studies, ensuring compliance with GCP and regulatory guidelines.
- Analyze and interpret clinical trial data to assess drug safety and efficacy.
- Prepare comprehensive study reports, scientific publications, and regulatory submissions.
- Collaborate with internal teams (e.g., R&D, regulatory, medical affairs) and external stakeholders (e.g., investigators, CROs).
- Manage budgets and timelines for assigned clinical trials.
- Identify and evaluate potential clinical investigators and sites.
- Provide scientific and technical expertise throughout the drug development process.
- Stay abreast of scientific advancements and therapeutic area developments.
- Contribute to the strategic direction of clinical development programs.
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Senior Clinical Research Scientist
NR2 1AA Norwich, Eastern
£55000 Annually
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Our client is looking for a highly skilled and experienced Senior Clinical Research Scientist to join their pioneering team in Norwich, Norfolk, UK . This role is integral to the advancement of our client's research and development pipeline, focusing on innovative scientific discovery and rigorous clinical validation. The ideal candidate will possess a strong background in medical research, clinical trials, and scientific data analysis, with a proven ability to lead complex research projects. You will be responsible for designing and executing clinical studies, overseeing data collection and analysis, and interpreting results to inform product development and regulatory submissions. Key responsibilities include developing study protocols, managing relationships with clinical sites and investigators, ensuring compliance with Good Clinical Practice (GCP) and other relevant regulations, and contributing to the scientific strategy of the organisation. You will also be involved in preparing research publications, presenting findings at scientific conferences, and mentoring junior research staff. The successful applicant will have a Ph.D. or Master's degree in a relevant scientific discipline (e.g., Biomedical Science, Pharmacology, Life Sciences), coupled with a minimum of 7 years of experience in clinical research. Extensive knowledge of study design, statistical analysis, and regulatory affairs is essential. Excellent project management, communication, and interpersonal skills are required to effectively collaborate with internal teams, external partners, and regulatory bodies. A deep understanding of the scientific and clinical aspects of the relevant therapeutic areas is crucial. This role offers a fantastic opportunity to contribute significantly to cutting-edge scientific advancements within a supportive and forward-thinking research environment.
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2
Clinical Research Scientist - Oncology
SW1A 0AA London, London
£50000 Annually
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Our client, a leading pharmaceutical company, is seeking a highly motivated Clinical Research Scientist to join their innovative oncology team based in London, England, UK . This role is critical in advancing groundbreaking cancer therapies from preclinical development through to clinical trials and regulatory approval. The successful candidate will be instrumental in designing, implementing, and managing clinical studies, ensuring adherence to Good Clinical Practice (GCP) and relevant regulatory guidelines. Responsibilities include developing study protocols, managing investigator sites, overseeing data collection and analysis, and preparing regulatory submissions. You will collaborate closely with cross-functional teams, including medical affairs, R&D, regulatory affairs, and marketing, to ensure the successful execution of clinical programs. A key aspect of this role involves staying at the forefront of scientific advancements in oncology, identifying new research opportunities, and contributing to the strategic direction of the company's drug development pipeline. The ideal candidate will possess a PhD or equivalent in a relevant scientific discipline (e.g., oncology, pharmacology, molecular biology) and have a minimum of 3-5 years of experience in clinical research within the pharmaceutical industry, specifically with oncology trials. Strong understanding of drug development processes, clinical trial methodologies, and regulatory requirements (e.g., FDA, EMA) is essential. Excellent analytical, problem-solving, and project management skills are required, along with outstanding written and verbal communication abilities. This position offers a competitive salary, comprehensive benefits package, and the opportunity to make a significant impact on the lives of cancer patients worldwide within a supportive and collaborative work environment.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and develop clinical trial protocols for oncology studies.
- Oversee the execution of clinical trials, ensuring compliance with GCP and regulatory standards.
- Manage relationships with clinical trial sites, investigators, and study personnel.
- Monitor study progress, data quality, and patient safety.
- Analyze clinical trial data and prepare study reports and publications.
- Contribute to regulatory submissions (e.g., IND, NDA).
- Collaborate with cross-functional teams to achieve project goals.
Qualifications:
- PhD or equivalent in Oncology, Pharmacology, or a related life science field.
- 3-5 years of experience in clinical research in the pharmaceutical industry, with a focus on oncology.
- Thorough knowledge of clinical trial design, conduct, and data analysis.
- Familiarity with GCP and relevant regulatory guidelines.
- Excellent scientific and medical writing skills.
- Strong project management and organizational abilities.
- Ability to work effectively in a team environment.
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3
Clinical Research Scientist - Oncology
CV1 1AA Coventry, West Midlands
£50000 Annually
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A leading pharmaceutical company with a significant presence in **Coventry, West Midlands, UK**, is seeking a highly skilled Clinical Research Scientist specializing in Oncology. This pivotal role involves contributing to the development of innovative cancer therapies, from early-stage research through to clinical trials. The successful candidate will be instrumental in designing, implementing, and analyzing complex research studies, ensuring compliance with regulatory standards and ethical guidelines.
Key responsibilities include developing research protocols, identifying and assessing suitable clinical trial sites, and managing relationships with investigators and study personnel. You will be involved in data collection, analysis, and interpretation, preparing comprehensive study reports, and presenting findings to internal and external stakeholders. This role requires a deep understanding of cancer biology, therapeutic targets, and the drug development process. You will collaborate closely with cross-functional teams, including regulatory affairs, biostatistics, and medical affairs, to ensure the successful execution of clinical programs.
The ideal candidate will hold a PhD or Master's degree in a relevant life science discipline (e.g., Pharmacology, Molecular Biology, Biochemistry, or a related field) and possess a minimum of 3-5 years of experience in clinical research, preferably within the oncology therapeutic area. Proven experience in clinical trial management, data analysis software (e.g., SAS, R), and strong knowledge of ICH-GCP guidelines are essential. Excellent written and verbal communication skills are required, along with the ability to work independently and as part of a team in a fast-paced environment. This position offers the opportunity to make a significant impact on the lives of cancer patients by advancing cutting-edge treatments. Join a company committed to scientific excellence and patient well-being.
Key responsibilities include developing research protocols, identifying and assessing suitable clinical trial sites, and managing relationships with investigators and study personnel. You will be involved in data collection, analysis, and interpretation, preparing comprehensive study reports, and presenting findings to internal and external stakeholders. This role requires a deep understanding of cancer biology, therapeutic targets, and the drug development process. You will collaborate closely with cross-functional teams, including regulatory affairs, biostatistics, and medical affairs, to ensure the successful execution of clinical programs.
The ideal candidate will hold a PhD or Master's degree in a relevant life science discipline (e.g., Pharmacology, Molecular Biology, Biochemistry, or a related field) and possess a minimum of 3-5 years of experience in clinical research, preferably within the oncology therapeutic area. Proven experience in clinical trial management, data analysis software (e.g., SAS, R), and strong knowledge of ICH-GCP guidelines are essential. Excellent written and verbal communication skills are required, along with the ability to work independently and as part of a team in a fast-paced environment. This position offers the opportunity to make a significant impact on the lives of cancer patients by advancing cutting-edge treatments. Join a company committed to scientific excellence and patient well-being.
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4
Senior Clinical Research Scientist
BS1 4RB Bristol, South West
£55000 Annually
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Posted 1 day ago
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Our client, a leading pharmaceutical innovator, is seeking a highly motivated and experienced Senior Clinical Research Scientist to join their dynamic, fully remote team. This pivotal role will involve contributing to the design, execution, and analysis of clinical trials for novel therapeutic agents. The successful candidate will be responsible for developing clinical protocols, overseeing study conduct, and ensuring compliance with regulatory guidelines and Good Clinical Practice (GCP). You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and data management, to ensure seamless trial progression. Key responsibilities include data review, interpretation of results, and contributing to scientific publications and presentations. This role requires a deep understanding of the pharmaceutical drug development process, strong analytical skills, and the ability to critically evaluate scientific data. The ideal candidate will possess excellent communication and interpersonal skills, enabling effective collaboration with internal stakeholders and external investigators. While the role is fully remote, fostering a connected and collaborative team environment is paramount. We are looking for individuals who are proactive, detail-oriented, and committed to advancing patient care through groundbreaking research. The ability to manage multiple projects simultaneously and meet strict deadlines is essential. A strong background in a relevant scientific discipline is required, with a preference for candidates with a PhD or equivalent experience in pharmacology, molecular biology, or a related field. Prior experience in clinical trial management, including study design, monitoring, and regulatory submissions, is highly desirable. Join a company that values innovation, scientific rigor, and offers a truly flexible working environment for its dedicated professionals.
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5
Clinical Research Scientist (Remote)
OX1 3AZ Oxford, South East
£55000 Annually
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Posted 4 days ago
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Our client, a globally recognized pharmaceutical leader, is actively seeking a dedicated Clinical Research Scientist to join their innovative research and development division. This is a fully remote position, offering flexibility and the opportunity to contribute to groundbreaking drug development from the comfort of your home office. You will be instrumental in designing, executing, and managing clinical trials for novel pharmaceutical agents across various therapeutic areas. Key responsibilities include developing clinical trial protocols, authoring Investigator's Brochures, and overseeing study conduct to ensure compliance with regulatory standards (e.g., GCP, ICH). You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and clinical operations, to ensure the successful progression of studies. This role requires meticulous attention to detail in analyzing clinical data, interpreting study results, and preparing comprehensive clinical study reports. You will also contribute to the preparation of regulatory submissions, such as INDs and NDAs. The ideal candidate will possess a Ph.D. or Master's degree in a relevant life science discipline (e.g., Pharmacology, Biotechnology, Molecular Biology) with a strong background in clinical research methodologies. A minimum of 5 years of experience in the pharmaceutical industry or a clinical research organization (CRO) is essential. Demonstrated experience in protocol development, clinical trial management, and regulatory documentation is required. Excellent scientific writing, verbal communication, and interpersonal skills are crucial for this remote role. Proficiency with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a plus. If you are a highly motivated scientist passionate about advancing patient care through innovative medicines and thrive in a remote work environment, we invite you to apply.
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Senior Clinical Research Scientist - Oncology
BS1 1AA Bristol, South West
£65000 Annually
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Posted 3 days ago
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Join our leading pharmaceutical company as a Senior Clinical Research Scientist specializing in Oncology, based remotely, serving clients and research sites across **Bristol, South West England, UK**, and beyond. This fully remote position allows you to contribute significantly to groundbreaking cancer research from the comfort of your home office. You will be responsible for the scientific and operational aspects of clinical trials, from protocol design through to study completion and data analysis. Your deep understanding of oncology drug development and clinical research methodologies will be crucial in driving forward innovative therapies.
Key Responsibilities:
Qualifications:
This is a pivotal role for an experienced scientist looking to make a substantial impact on cancer patient care through innovative research in a flexible, remote environment.
Key Responsibilities:
- Lead the design and development of clinical trial protocols, informed consent forms, and other study-related documents in oncology.
- Provide scientific and clinical expertise throughout the trial lifecycle, ensuring adherence to GCP and regulatory guidelines.
- Oversee the selection and qualification of clinical trial sites and investigators.
- Collaborate with cross-functional teams, including medical affairs, regulatory affairs, data management, and statistics.
- Monitor study progress, interpret emerging data, and make recommendations for study adjustments.
- Prepare clinical study reports, regulatory submissions, and scientific publications.
- Manage relationships with contract research organizations (CROs) and other external vendors.
- Stay current with scientific advancements, emerging therapies, and regulatory changes in oncology.
- Contribute to the strategic planning and direction of the company's oncology pipeline.
Qualifications:
- PhD or PharmD in a relevant life science discipline; MD is also acceptable.
- Minimum of 5-7 years of experience in clinical research, preferably within the pharmaceutical or biotech industry, with a strong focus on oncology.
- Demonstrated experience in clinical trial design, execution, and data analysis.
- In-depth knowledge of oncology, including various cancer types, treatment modalities, and drug development pathways.
- Familiarity with regulatory requirements (FDA, EMA) and ICH-GCP guidelines.
- Excellent scientific writing and communication skills.
- Ability to work independently, manage multiple projects simultaneously, and meet deadlines in a remote setting.
- Proficiency in data analysis tools and software commonly used in clinical research.
This is a pivotal role for an experienced scientist looking to make a substantial impact on cancer patient care through innovative research in a flexible, remote environment.
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Senior Clinical Research Scientist - Oncology
SO14 0EQ Southampton, South East
£60000 Annually
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Posted 3 days ago
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Our client, a leading innovator in the pharmaceutical sector, is seeking a highly motivated and experienced Senior Clinical Research Scientist with a specialization in Oncology to join their dynamic, fully remote team. This pivotal role will involve the design, execution, and analysis of complex clinical trials, contributing significantly to the development of life-saving cancer therapies. You will be responsible for developing study protocols, managing statistical analysis plans, and interpreting clinical data to drive strategic decision-making. Key Responsibilities:
- Design and implement Phase I-III clinical trial protocols for novel oncology treatments.
- Oversee data collection, monitoring, and statistical analysis to ensure accuracy and compliance with regulatory standards (e.g., ICH-GCP).
- Collaborate with cross-functional teams, including medical affairs, regulatory affairs, and drug discovery, to ensure seamless trial progression.
- Prepare high-quality clinical study reports, manuscripts for publication, and presentations for scientific conferences.
- Provide scientific and strategic input into the overall drug development program.
- Manage external collaborations with academic institutions and contract research organizations (CROs).
- Ensure adherence to all relevant ethical guidelines and regulatory requirements throughout the trial lifecycle.
- Mentor junior research scientists and contribute to the scientific growth of the department.
- PhD or equivalent in a relevant scientific discipline (e.g., Pharmacology, Biology, Medicine).
- Minimum of 5-7 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry, with a strong focus on Oncology.
- Demonstrated success in designing and executing clinical trials, preferably in solid tumors or hematological malignancies.
- In-depth understanding of statistical principles and clinical data analysis techniques.
- Excellent written and verbal communication skills, with a proven ability to present complex scientific information clearly and concisely.
- Strong project management skills and the ability to manage multiple priorities in a fast-paced, remote environment.
- Proficiency in relevant software, including EDC systems and statistical analysis software (e.g., SAS, R).
- Ability to work independently and collaboratively as part of a global, remote team.
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8
Senior Clinical Research Scientist - Oncology
WV1 1AD Wolverhampton, West Midlands
£70000 Annually
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Posted 4 days ago
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Job Description
Our client is seeking a highly motivated and experienced Senior Clinical Research Scientist to join their pioneering pharmaceutical research team. This is a fully remote position, offering the flexibility to work from anywhere within the UK. You will play a critical role in the design, execution, and analysis of cutting-edge clinical trials focused on oncology treatments. Your responsibilities will include developing study protocols, contributing to regulatory submissions, and managing data integrity to ensure compliance with all relevant guidelines. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, and data management, to drive research objectives forward. This role requires a deep understanding of pharmaceutical drug development processes, particularly in oncology, and a proven track record in clinical trial management. Excellent communication and interpersonal skills are essential for effective collaboration with internal stakeholders and external research partners. You will also be responsible for identifying and mitigating risks associated with clinical trials, ensuring patient safety and data accuracy throughout the trial lifecycle. The ideal candidate will possess strong analytical skills, the ability to interpret complex scientific data, and a passion for advancing cancer therapies. Your expertise will be vital in contributing to the development of novel treatments that have the potential to significantly improve patient outcomes.
Responsibilities:
Responsibilities:
- Lead the scientific design and development of clinical trial protocols for oncology studies.
- Contribute to the preparation and submission of regulatory documents (e.g., IND, NDA).
- Oversee data collection, cleaning, and analysis, ensuring accuracy and completeness.
- Monitor trial progress and identify potential risks and challenges, implementing mitigation strategies.
- Collaborate with principal investigators and study site staff to ensure protocol adherence.
- Prepare scientific reports, publications, and presentations.
- Stay abreast of the latest advancements in oncology research and clinical trial methodologies.
- Mentor junior members of the research team.
- Ensure all research activities are conducted in compliance with GCP, ICH guidelines, and other applicable regulations.
- PhD or equivalent in a relevant scientific field (e.g., Pharmacology, Biology, Oncology).
- Minimum of 5-7 years of experience in clinical research within the pharmaceutical industry, with a focus on oncology.
- Demonstrable experience in designing and managing Phase I-III clinical trials.
- Strong understanding of oncology drug development and relevant therapeutic areas.
- Excellent knowledge of regulatory requirements (FDA, EMA) and Good Clinical Practice (GCP).
- Exceptional analytical, problem-solving, and critical thinking skills.
- Proficiency in statistical analysis software and clinical data management systems.
- Superior written and verbal communication skills.
- Ability to work independently and as part of a remote, collaborative team.
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