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.1,699 Clinical Research jobs in the United Kingdom
Remote Senior Clinical Data Manager
B1 1 Birmingham, West Midlands
£60000 Annually
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Posted 3 days ago
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Job Description
Our client, a forward-thinking pharmaceutical research organization, is seeking an experienced Senior Clinical Data Manager to join their global team on a fully remote basis. This vital position will play a key role in ensuring the accuracy, integrity, and completeness of clinical trial data, which is fundamental to the success of our drug development programs. The ideal candidate will have a robust understanding of clinical trial processes, data management principles, and relevant regulatory requirements (e.g., FDA, EMA). You will be responsible for developing data management plans, overseeing database design and validation, managing data cleaning activities, and ensuring timely database lock. This role is perfectly suited for a seasoned data professional who is highly organized, detail-oriented, and proficient in managing complex projects in a remote work environment.
Key Responsibilities:
The ideal candidate will possess a Bachelor's degree in a relevant scientific discipline (e.g., Health Informatics, Statistics, Computer Science) or equivalent experience. A minimum of 7 years of progressive experience in clinical data management within the pharmaceutical or biotechnology industry is required, with at least 2 years in a lead or senior role. Expertise with major EDC systems (e.g., Medidata Rave, Oracle Clinical, Veeva EDC) is essential. Proficiency in CDISC standards (SDTM, ADaM) is highly desirable. Strong understanding of GCP and regulatory requirements for clinical trials is mandatory. Excellent problem-solving, organizational, and project management skills are necessary. The ability to work independently, manage multiple studies concurrently, and meet tight deadlines in a remote environment is crucial. Exceptional communication skills, both written and verbal, are needed to collaborate effectively with global teams.
Key Responsibilities:
- Develop and implement comprehensive Clinical Data Management Plans (CDMPs).
- Oversee the design, build, and validation of clinical databases using EDC systems.
- Develop data validation specifications and perform data review and cleaning activities.
- Manage query generation, resolution, and tracking to ensure data accuracy.
- Lead the process for database lock, ensuring all data is complete and validated.
- Ensure compliance with relevant regulatory guidelines (e.g., GCP, ICH, CDISC) and company SOPs.
- Liaise with clinical operations, biostatistics, and programming teams to ensure seamless data flow.
- Provide technical expertise and guidance to junior data managers and study team members.
- Contribute to the development and maintenance of data management tools and processes.
- Manage outsourced data management activities with CROs, as applicable.
The ideal candidate will possess a Bachelor's degree in a relevant scientific discipline (e.g., Health Informatics, Statistics, Computer Science) or equivalent experience. A minimum of 7 years of progressive experience in clinical data management within the pharmaceutical or biotechnology industry is required, with at least 2 years in a lead or senior role. Expertise with major EDC systems (e.g., Medidata Rave, Oracle Clinical, Veeva EDC) is essential. Proficiency in CDISC standards (SDTM, ADaM) is highly desirable. Strong understanding of GCP and regulatory requirements for clinical trials is mandatory. Excellent problem-solving, organizational, and project management skills are necessary. The ability to work independently, manage multiple studies concurrently, and meet tight deadlines in a remote environment is crucial. Exceptional communication skills, both written and verbal, are needed to collaborate effectively with global teams.
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Clinical Research Scientist
B1 1BB Birmingham, West Midlands
£55000 Annually
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Posted today
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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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1
Lead Clinical Research Scientist
NE1 4AG Newcastle upon Tyne, North East
£75000 Annually
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Our client is seeking a highly qualified and experienced Lead Clinical Research Scientist to spearhead groundbreaking research initiatives. This role is integral to our client's commitment to scientific advancement and will involve leading projects from inception through to completion. You will be responsible for designing and executing complex experiments, analyzing research data, and interpreting results to drive new discoveries. A key aspect of your role will be managing research teams, mentoring junior scientists, and fostering a collaborative and innovative research environment. You will also be involved in preparing research proposals, securing funding, and disseminating findings through publications and presentations. The ideal candidate will possess a Ph.D. in a relevant scientific discipline (e.g., biology, chemistry, medicine), coupled with extensive post-doctoral experience and a strong publication record. Proven leadership experience in a research setting is essential. You should have expertise in advanced research methodologies, analytical techniques, and laboratory management. Familiarity with regulatory requirements and ethical considerations in scientific research is crucial. Excellent communication, critical thinking, and problem-solving skills are required. You will collaborate with internal teams, external partners, and academic institutions. This position offers a challenging and rewarding opportunity to contribute to significant scientific advancements and lead cutting-edge research within a dynamic organization. Your expertise will be vital in advancing our understanding and developing novel solutions in your field of specialization.
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2
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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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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4
Senior Clinical Research Scientist
M1 1AA Manchester, North West
£55000 Annually
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Our client is seeking a highly motivated and experienced Senior Clinical Research Scientist to join their dynamic team in **Manchester, Greater Manchester, UK**. This role is crucial in advancing innovative pharmaceutical research and development, focusing on late-stage clinical trials. The successful candidate will play a pivotal role in the design, execution, and analysis of clinical studies, ensuring compliance with regulatory standards and company protocols.
Key Responsibilities:
Key Responsibilities:
- Lead the scientific design and oversight of Phase II and III clinical trials, including protocol development, investigator brochure writing, and statistical analysis plans.
- Collaborate closely with cross-functional teams, including medical affairs, regulatory, data management, and clinical operations, to ensure seamless trial execution.
- Interpret complex clinical data, prepare clinical study reports, and contribute to regulatory submissions (e.g., IND, NDA).
- Manage external collaborations with Key Opinion Leaders (KOLs), academic institutions, and contract research organizations (CROs).
- Stay abreast of the latest scientific advancements, therapeutic area trends, and competitive landscape to identify new research opportunities.
- Mentor junior scientists and contribute to the development of departmental standard operating procedures (SOPs) and best practices.
- Present research findings at scientific conferences and contribute to publications in peer-reviewed journals.
- Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and all relevant local and international regulations.
- PhD or PharmD in a relevant scientific discipline (e.g., Pharmacology, Biochemistry, Medicine).
- Minimum of 5-7 years of experience in clinical research within the pharmaceutical industry, with a strong focus on oncology or a related therapeutic area.
- Proven track record of successfully designing and managing clinical trials from concept to completion.
- Deep understanding of drug development processes, clinical trial methodologies, and regulatory requirements.
- Excellent analytical, problem-solving, and critical-thinking skills.
- Strong communication, interpersonal, and presentation skills, with the ability to effectively collaborate with diverse stakeholders.
- Demonstrated ability to manage multiple projects simultaneously in a fast-paced environment.
- Proficiency in statistical software and data analysis tools is a plus.
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5
Clinical Research Scientist - Oncology
CV1 1AA Coventry, West Midlands
£50000 Annually
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Posted 1 day ago
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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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Senior Clinical Research Scientist
BS1 4RB Bristol, South West
£55000 Annually
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Posted 2 days 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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7
Clinical Research Scientist (Remote)
OX1 3AZ Oxford, South East
£55000 Annually
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Posted 5 days ago
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Job Description
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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8
Lead Clinical Research Scientist (Oncology)
AB10 1AA Aberdeen, Scotland
£70000 Annually
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Our client is seeking an experienced and dedicated Lead Clinical Research Scientist specializing in Oncology to join their prestigious pharmaceutical research division. This fully remote position offers a unique opportunity to contribute to groundbreaking drug development efforts from anywhere within the UK. You will be responsible for designing, implementing, and managing complex clinical trials, ensuring adherence to all regulatory guidelines and ethical standards. This includes protocol development, site selection and initiation, data monitoring, and analysis. You will play a crucial role in interpreting trial results, preparing scientific publications, and presenting findings to internal stakeholders and regulatory bodies. Collaboration is key; you will work closely with principal investigators, study coordinators, statisticians, and regulatory affairs specialists to ensure the smooth execution of clinical studies. Your expertise will be vital in identifying potential risks, developing mitigation strategies, and ensuring the safety and efficacy of investigational medicinal products. We are looking for a proactive individual with a deep understanding of oncological diseases and current therapeutic strategies. You will also be involved in the mentorship of junior research staff and contribute to the strategic planning of the clinical development pipeline. The ideal candidate will have a strong track record of success in clinical trial management, excellent scientific writing skills, and a passion for advancing cancer therapies. This role requires a strong scientific background, exceptional analytical abilities, and outstanding interpersonal and communication skills, enabling effective remote collaboration. This is an exceptional opportunity to shape the future of oncology treatment within a leading pharmaceutical organisation, based in Aberdeen, Scotland, UK .
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