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.6,841 Clinical Research jobs in the United Kingdom
Clinical Research Scientist
NG1 1GG Nottingham, East Midlands
£55000 Annually
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Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical company dedicated to advancing global health, is looking for a highly skilled and motivated Clinical Research Scientist to join their esteemed research and development team based in Nottingham, Nottinghamshire, UK . This critical role involves contributing to the design, execution, and analysis of clinical trials for novel therapeutic agents. You will be responsible for the scientific integrity of clinical studies, ensuring compliance with regulatory requirements and ethical standards. Key duties include developing clinical protocols, managing data collection and analysis, interpreting study results, and preparing scientific reports and publications. You will collaborate closely with internal teams, including R&D, regulatory affairs, and medical affairs, as well as external stakeholders such as investigators, ethics committees, and contract research organizations (CROs). The ideal candidate will possess a Ph.D. or Master's degree in a relevant life science discipline (e.g., pharmacology, biology, medicine) with significant experience in clinical research within the pharmaceutical industry. A strong understanding of drug development processes, Good Clinical Practice (GCP) guidelines, and regulatory frameworks (e.g., FDA, EMA) is essential. Excellent scientific writing, communication, and interpersonal skills are required to effectively present complex data and engage with diverse audiences. This is an exciting opportunity to contribute to the development of life-changing medicines and advance your career in a dynamic and supportive environment. The role requires presence in our Nottingham facility to facilitate essential in-person collaboration and laboratory work.
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Clinical Research Scientist
CF10 1DA Cardiff, Wales
£60000 Annually
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Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical company committed to improving global health, is seeking a dedicated and experienced Clinical Research Scientist to join their dynamic team in **Cardiff**, Wales. This role is integral to the design, execution, and interpretation of clinical trials for novel therapeutic agents. You will play a key part in bringing life-changing medicines to patients by ensuring the highest standards of scientific integrity and regulatory compliance throughout the clinical development process. The ideal candidate will possess a strong scientific background, extensive experience in clinical trial management, and a deep understanding of regulatory guidelines (e.g., ICH-GCP). Responsibilities include developing clinical trial protocols, overseeing study conduct, managing data analysis and interpretation, and preparing regulatory submissions. You will collaborate closely with internal teams, including R&D, regulatory affairs, and project management, as well as external partners such as investigators, site staff, and contract research organizations (CROs). This position requires exceptional analytical, problem-solving, and communication skills, as well as the ability to work effectively in a collaborative, fast-paced environment. This role is office-based in **Cardiff**. We offer a competitive salary, comprehensive benefits package, and opportunities for professional growth and development within a company that values innovation and scientific excellence.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and develop clinical trial protocols in accordance with scientific objectives and regulatory requirements.
- Oversee the execution of clinical trials, ensuring compliance with ICH-GCP and other relevant regulations.
- Manage study timelines, budgets, and resources effectively.
- Collaborate with investigators and clinical site staff to ensure high-quality data collection.
- Analyze and interpret clinical trial data, contributing to study reports and publications.
- Prepare study-related documents, including investigator brochures, case report forms, and regulatory submission dossiers.
- Liaise with regulatory authorities and ethics committees.
- Contribute to the scientific strategy for drug development programs.
- Mentor and guide junior research staff.
Qualifications:
- PhD or Master's degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Minimum of 5 years of experience in clinical research and development within the pharmaceutical industry.
- Thorough understanding of clinical trial design, execution, and data analysis.
- In-depth knowledge of ICH-GCP guidelines and regulatory submission processes.
- Excellent scientific writing, analytical, and problem-solving skills.
- Strong interpersonal and communication skills, with the ability to build effective relationships.
- Experience in (Specific Therapeutic Area, e.g., Oncology, Cardiology) is a plus.
- Proficiency in relevant clinical trial management systems and statistical software.
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1
Clinical Research Scientist
SW1A 0AA London, London
£65000 Annually
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Posted 3 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is looking for an innovative Clinical Research Scientist to contribute to groundbreaking drug development from the comfort of their home. This is a fully remote position, offering the flexibility to work from anywhere within the UK, with a focus on designing and executing clinical trials that will shape the future of medicine. You will be responsible for the scientific integrity of clinical studies, from protocol development through to final study report.
Key responsibilities include analyzing complex data sets, interpreting results, and presenting findings to internal stakeholders and regulatory bodies. You will collaborate closely with cross-functional teams, including statisticians, medical writers, and regulatory affairs specialists, to ensure compliance with all relevant guidelines and regulations. This role demands a deep understanding of pharmaceutical research methodologies, statistical analysis, and regulatory requirements (e.g., GCP, ICH). A PhD or equivalent in a relevant life science discipline (e.g., pharmacology, biochemistry, molecular biology) is highly preferred, along with a proven track record of successfully managing clinical trials.
The ideal candidate will possess exceptional analytical skills, a meticulous attention to detail, and the ability to work independently with minimal supervision. Strong written and verbal communication skills are essential for documenting research, writing manuscripts for publication, and presenting scientific information clearly and concisely. You should be adept at managing multiple projects simultaneously and meeting tight deadlines. This is an exceptional opportunity to join a forward-thinking organization and make a significant impact on global health, working on cutting-edge therapies. Your expertise will be crucial in bringing life-changing treatments to patients worldwide. Embrace the future of pharmaceutical research in this exciting remote role.
Key responsibilities include analyzing complex data sets, interpreting results, and presenting findings to internal stakeholders and regulatory bodies. You will collaborate closely with cross-functional teams, including statisticians, medical writers, and regulatory affairs specialists, to ensure compliance with all relevant guidelines and regulations. This role demands a deep understanding of pharmaceutical research methodologies, statistical analysis, and regulatory requirements (e.g., GCP, ICH). A PhD or equivalent in a relevant life science discipline (e.g., pharmacology, biochemistry, molecular biology) is highly preferred, along with a proven track record of successfully managing clinical trials.
The ideal candidate will possess exceptional analytical skills, a meticulous attention to detail, and the ability to work independently with minimal supervision. Strong written and verbal communication skills are essential for documenting research, writing manuscripts for publication, and presenting scientific information clearly and concisely. You should be adept at managing multiple projects simultaneously and meeting tight deadlines. This is an exceptional opportunity to join a forward-thinking organization and make a significant impact on global health, working on cutting-edge therapies. Your expertise will be crucial in bringing life-changing treatments to patients worldwide. Embrace the future of pharmaceutical research in this exciting remote role.
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2
Clinical Research Scientist
NG1 1 Nottingham, East Midlands
£55000 Annually
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Posted 3 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is seeking a highly skilled and motivated Clinical Research Scientist to join their innovative, fully remote research and development team. This crucial role will involve contributing to the design, execution, and analysis of clinical trials, with a focus on (Specific therapeutic area, e.g., oncology, immunology, rare diseases). You will be instrumental in advancing novel drug candidates through the development pipeline, from pre-clinical research to regulatory submission. The ideal candidate will possess a strong scientific background, meticulous attention to detail, and the ability to thrive in a fast-paced, virtual research environment. This is an exceptional opportunity to contribute to life-changing medical advancements from the comfort of your home.
Responsibilities:
Responsibilities:
- Contribute to the design and development of clinical trial protocols, ensuring scientific integrity and regulatory compliance.
- Oversee the execution of clinical trials, including site selection, investigator meetings, and monitoring activities.
- Analyze and interpret complex clinical data, preparing comprehensive reports and presentations for internal stakeholders and regulatory agencies.
- Collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and project management.
- Stay abreast of the latest scientific literature, emerging technologies, and regulatory guidelines relevant to clinical research.
- Contribute to the writing of investigational new drug (IND) applications, clinical study reports (CSRs), and manuscripts for publication.
- Identify and mitigate risks associated with clinical trial execution.
- Manage relationships with external collaborators, key opinion leaders (KOLs), and contract research organizations (CROs).
- Contribute to the development of scientific strategies and pipeline planning.
- Ensure all research activities are conducted in compliance with Good Clinical Practice (GCP) guidelines and company policies.
- Ph.D. or Master's degree in a relevant scientific discipline (e.g., life sciences, pharmacology, biomedical science).
- Minimum of 5 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry.
- Demonstrated experience in designing, conducting, and analyzing clinical trials.
- Strong understanding of drug development processes and regulatory requirements (e.g., FDA, EMA).
- Excellent scientific writing and data analysis skills.
- Proficiency in statistical software and data management systems is a plus.
- Exceptional communication, collaboration, and interpersonal skills.
- Ability to work independently, manage multiple projects simultaneously, and meet tight deadlines in a remote setting.
- Experience in (Specific therapeutic area) is highly desirable.
- Proven ability to critically evaluate scientific data and contribute to strategic decision-making.
- Must have a dedicated home office setup with reliable high-speed internet to perform duties effectively.
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3
Lead Clinical Research Scientist
NE2 4HP Newcastle upon Tyne, North East
£65000 Annually
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Our client, a global leader in pharmaceutical innovation, is looking for a highly motivated and experienced Lead Clinical Research Scientist to join their esteemed research and development division based in **Newcastle upon Tyne, Tyne and Wear, UK**. This critical role will spearhead groundbreaking research projects focused on developing novel therapeutics and improving patient outcomes.
The Lead Clinical Research Scientist will be responsible for the design, execution, and interpretation of clinical studies. This includes developing study protocols, overseeing patient recruitment and data collection, and ensuring compliance with regulatory guidelines and ethical standards. You will work collaboratively with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and data management, to ensure the successful progression of research programs from early-stage development through to regulatory submission.
Key responsibilities include:
The Lead Clinical Research Scientist will be responsible for the design, execution, and interpretation of clinical studies. This includes developing study protocols, overseeing patient recruitment and data collection, and ensuring compliance with regulatory guidelines and ethical standards. You will work collaboratively with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and data management, to ensure the successful progression of research programs from early-stage development through to regulatory submission.
Key responsibilities include:
- Leading the scientific strategy for clinical development programs in specific therapeutic areas.
- Designing and managing clinical trial protocols, ensuring scientific rigor and alignment with regulatory requirements.
- Overseeing the conduct of clinical trials, including site selection, investigator training, and monitoring.
- Analyzing and interpreting complex clinical data, and contributing to the preparation of clinical study reports and regulatory submission documents.
- Collaborating with internal and external experts, including key opinion leaders (KOLs) and academic institutions.
- Ensuring adherence to Good Clinical Practice (GCP) guidelines and all relevant regulations.
- Mentoring and guiding junior scientists and research staff.
- Contributing to the development of publications and presentations for scientific conferences.
- Staying current with the latest scientific advancements and therapeutic trends in the pharmaceutical industry.
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4
Clinical Research Scientist - Pharmaceutical
SO14 0AA Southampton, South East
£65000 Annually
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Posted 3 days ago
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Job Description
Our client, a globally recognised pharmaceutical innovator, is actively seeking a highly qualified and dedicated Clinical Research Scientist to join their cutting-edge research team on a fully remote basis. This is an exceptional opportunity to contribute to the development of life-changing therapies and be part of a company committed to scientific excellence and patient well-being. As a remote-first organisation, we foster a collaborative and flexible working environment.
In this critical role, you will be responsible for the scientific design, planning, and execution of clinical trials for novel pharmaceutical compounds. Your duties will include developing clinical protocols, study plans, and investigator brochures, ensuring adherence to regulatory guidelines (e.g., ICH-GCP) and scientific rigor. You will collaborate closely with cross-functional teams, including biostatistics, data management, regulatory affairs, and clinical operations, to ensure seamless trial conduct. A key aspect of your role will involve analysing and interpreting clinical data, contributing to the development of clinical study reports (CSRs) and scientific publications. You will also provide scientific expertise and support to study teams, investigators, and external stakeholders. Staying abreast of the latest scientific literature, emerging technologies, and competitive intelligence within your therapeutic area will be essential. You may also contribute to regulatory submissions and interactions with health authorities.
The ideal candidate will hold a PhD or Master's degree in a life science discipline (e.g., Pharmacology, Biology, Biochemistry, Medicine) with a strong background in clinical research. Proven experience in designing and managing Phase I, II, or III clinical trials within the pharmaceutical industry is required. You should possess a comprehensive understanding of drug development processes, regulatory requirements, and scientific methodologies. Excellent analytical, critical thinking, and problem-solving skills are paramount. Superior written and verbal communication skills are essential for authoring protocols, reports, and publications, as well as for effectively collaborating with diverse teams. The ability to work independently, manage multiple projects simultaneously, and thrive in a remote, fast-paced environment is crucial. Experience in a specific therapeutic area relevant to our client's pipeline would be a significant advantage.
We offer a highly competitive salary, comprehensive benefits package, and significant opportunities for professional development and career advancement. Join our client's dedicated team and contribute to advancing global health through pioneering pharmaceutical research, all within a supportive remote work structure.
In this critical role, you will be responsible for the scientific design, planning, and execution of clinical trials for novel pharmaceutical compounds. Your duties will include developing clinical protocols, study plans, and investigator brochures, ensuring adherence to regulatory guidelines (e.g., ICH-GCP) and scientific rigor. You will collaborate closely with cross-functional teams, including biostatistics, data management, regulatory affairs, and clinical operations, to ensure seamless trial conduct. A key aspect of your role will involve analysing and interpreting clinical data, contributing to the development of clinical study reports (CSRs) and scientific publications. You will also provide scientific expertise and support to study teams, investigators, and external stakeholders. Staying abreast of the latest scientific literature, emerging technologies, and competitive intelligence within your therapeutic area will be essential. You may also contribute to regulatory submissions and interactions with health authorities.
The ideal candidate will hold a PhD or Master's degree in a life science discipline (e.g., Pharmacology, Biology, Biochemistry, Medicine) with a strong background in clinical research. Proven experience in designing and managing Phase I, II, or III clinical trials within the pharmaceutical industry is required. You should possess a comprehensive understanding of drug development processes, regulatory requirements, and scientific methodologies. Excellent analytical, critical thinking, and problem-solving skills are paramount. Superior written and verbal communication skills are essential for authoring protocols, reports, and publications, as well as for effectively collaborating with diverse teams. The ability to work independently, manage multiple projects simultaneously, and thrive in a remote, fast-paced environment is crucial. Experience in a specific therapeutic area relevant to our client's pipeline would be a significant advantage.
We offer a highly competitive salary, comprehensive benefits package, and significant opportunities for professional development and career advancement. Join our client's dedicated team and contribute to advancing global health through pioneering pharmaceutical research, all within a supportive remote work structure.
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5
Senior Clinical Research Scientist
LE1 5AA Leicester, East Midlands
£70000 Annually
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Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking an experienced Senior Clinical Research Scientist to join their dedicated team in Leicester, Leicestershire, UK . This crucial role will involve designing, implementing, and managing clinical trials, ensuring adherence to regulatory standards and contributing to the development of innovative therapeutics. You will play a key part in evaluating drug efficacy and safety, analyzing data, and preparing essential documentation for regulatory submissions. The ideal candidate will possess a strong scientific background, extensive experience in clinical trial management, and excellent analytical and communication skills.
Responsibilities:
Responsibilities:
- Designing clinical trial protocols in collaboration with cross-functional teams and investigators.
- Overseeing the execution of clinical trials, ensuring compliance with Good Clinical Practice (GCP) guidelines and relevant regulations.
- Managing relationships with clinical sites, contract research organizations (CROs), and other external partners.
- Monitoring trial progress, data integrity, and patient safety throughout the study lifecycle.
- Analyzing and interpreting clinical trial data, contributing to study reports and publications.
- Preparing essential regulatory documents, including Investigational New Drug (IND) applications and New Drug Applications (NDAs).
- Providing scientific and technical expertise to internal teams and external stakeholders.
- Contributing to the evaluation of new drug candidates and development strategies.
- Ensuring timely completion of trials within budget.
- Staying abreast of scientific advancements and regulatory changes in the pharmaceutical industry.
- Advanced degree (MSc, PhD) in a life science, medical, or related field.
- Minimum of 7 years of experience in clinical research, preferably within the pharmaceutical industry.
- In-depth knowledge of clinical trial design, methodology, and regulatory requirements (e.g., FDA, EMA, ICH guidelines).
- Proven experience in managing multiple clinical trials simultaneously.
- Strong understanding of biostatistics and data analysis principles.
- Excellent scientific writing and communication skills, with experience in preparing regulatory submissions.
- Ability to work effectively in a multidisciplinary team environment.
- Strong problem-solving and decision-making abilities.
- Proficiency in clinical trial management software and data analysis tools.
- Leadership qualities and experience in mentoring junior staff are desirable.
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Senior Clinical Research Scientist
B3 2PY Birmingham, West Midlands
£70000 Annually
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Posted 3 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is seeking a highly qualified and experienced Senior Clinical Research Scientist to join their innovative team. This is a fully remote position, allowing you to contribute significantly to groundbreaking drug development from the comfort of your home. The role involves the design, execution, and interpretation of clinical trials, contributing to the advancement of novel therapies. The successful candidate will play a crucial role in ensuring the scientific integrity and operational success of clinical research programs.
Key Responsibilities:
Key Responsibilities:
- Lead the design and development of clinical trial protocols, ensuring scientific rigor and alignment with regulatory requirements.
- Oversee the execution of clinical trials, providing scientific and technical guidance to study teams.
- Analyze and interpret complex clinical trial data, preparing comprehensive study reports and publications.
- Collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and project management.
- Contribute to the development of Investigator's Brochures, Clinical Study Reports, and regulatory submission documents.
- Evaluate the safety and efficacy of investigational medicinal products based on trial data.
- Stay current with scientific literature, clinical trial methodologies, and regulatory guidelines.
- Represent the company at scientific meetings and conferences, presenting research findings.
- Mentor junior scientists and contribute to the development of scientific expertise within the organization.
- Manage external collaborations with investigators, key opinion leaders, and research institutions through effective remote communication.
- PhD or equivalent in a relevant life science discipline (e.g., Pharmacology, Molecular Biology, Medicine).
- Minimum of 5-7 years of experience in clinical research within the pharmaceutical or biotechnology industry.
- Proven experience in clinical trial design, execution, and data analysis.
- Strong understanding of Good Clinical Practice (GCP) and relevant regulatory guidelines (e.g., FDA, EMA).
- Excellent scientific knowledge and critical thinking skills.
- Proficiency in statistical analysis of clinical data and interpretation of results.
- Exceptional written and verbal communication skills, with a track record of publications and presentations.
- Demonstrated ability to work independently and lead projects in a remote setting.
- Experience in specific therapeutic areas (e.g., oncology, immunology, neurology) is highly desirable.
- Familiarity with the Birmingham, West Midlands, UK pharmaceutical landscape is a plus, but not essential for this remote role.
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7
Senior Clinical Research Scientist
B3 2BB Birmingham, West Midlands
£55000 Annually
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Posted 3 days ago
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Job Description
Our client, a leading pharmaceutical company, is looking for a highly motivated Senior Clinical Research Scientist to join their innovative team in **Birmingham, West Midlands, UK**. This role is integral to the design, execution, and interpretation of clinical trials, contributing to the development of groundbreaking therapies. You will be responsible for scientific leadership within clinical development teams, ensuring the integrity and quality of clinical study data. Key responsibilities include developing clinical trial protocols, Investigator's Brochures, and clinical study reports, often in collaboration with external experts. You will play a crucial role in site selection and initiation, providing scientific support to clinical investigators and site staff. The Senior Clinical Research Scientist will also be involved in data analysis and interpretation, ensuring alignment with regulatory requirements and scientific objectives. You will contribute to the preparation of regulatory submissions and interact with health authorities. This position requires a deep understanding of drug development processes, clinical pharmacology, and relevant therapeutic areas. The successful candidate will possess excellent scientific writing skills, strong analytical capabilities, and the ability to critically evaluate scientific literature. A proactive approach to problem-solving and a collaborative spirit are essential. This is an excellent opportunity to contribute to patient health by advancing novel medicines through the development pipeline. You will work in a fast-paced, cutting-edge environment, engaging with diverse teams across research, development, and medical affairs. The role demands a high degree of autonomy and accountability, with the opportunity to influence strategic decisions in clinical development. We are seeking a candidate with a strong scientific background and a passion for innovation in pharmaceutical research.
Responsibilities:
Responsibilities:
- Lead the scientific aspects of clinical trial design and execution.
- Develop and write clinical trial protocols, Investigator's Brochures, and Clinical Study Reports.
- Provide scientific and medical expertise to clinical development teams.
- Oversee data interpretation and ensure scientific rigor.
- Liaise with regulatory authorities and prepare submission documents.
- Support site selection, initiation, and ongoing monitoring of clinical trials.
- Stay abreast of scientific advancements and competitive landscape within therapeutic areas.
- Collaborate with external Key Opinion Leaders and investigators.
- Advanced degree (MSc, PhD, MD) in a life science or medical discipline.
- Minimum of 5-7 years of experience in clinical research within the pharmaceutical industry.
- Proven experience in designing and managing Phase II/III clinical trials.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Excellent written and verbal communication skills.
- Strong analytical and critical thinking abilities.
- Experience in oncology or a specific therapeutic area is highly desirable.
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8
Lead Clinical Research Scientist
CV1 2TT Coventry, West Midlands
£60000 Annually
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Posted 3 days ago
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Job Description
Our client is a leading pharmaceutical company dedicated to discovering and developing innovative medicines. We are seeking a highly motivated and experienced Lead Clinical Research Scientist to join our team based in **Coventry, West Midlands, UK**. This role offers a hybrid working model, combining the benefits of in-office collaboration with remote flexibility. You will play a crucial role in the design, execution, and interpretation of clinical trials, contributing significantly to bringing life-changing therapies to patients.
Responsibilities:
Qualifications:
This is an exciting opportunity to contribute to cutting-edge pharmaceutical research and development within a supportive and innovative environment. The hybrid working arrangement allows for a balance between focused individual work and collaborative team engagement at our **Coventry** facilities.
Responsibilities:
- Lead the scientific and strategic direction of clinical development programs.
- Design and oversee the development of clinical trial protocols, ensuring scientific rigor and regulatory compliance.
- Provide expert input on study design, endpoint selection, statistical analysis plans, and data interpretation.
- Collaborate with cross-functional teams, including clinical operations, regulatory affairs, medical affairs, and biostatistics.
- Manage relationships with external investigators, key opinion leaders, and other external stakeholders.
- Critically evaluate scientific literature and data to support study design and decision-making.
- Prepare and present scientific data at internal meetings and external conferences.
- Contribute to the preparation of regulatory submissions and publications.
- Mentor and guide junior members of the clinical science team.
- Ensure adherence to all relevant ethical, regulatory, and GCP guidelines throughout the trial lifecycle.
Qualifications:
- Advanced degree (MSc, PhD, MD, PharmD) in a relevant scientific or medical discipline.
- Significant experience (typically 7+ years) in clinical research within the pharmaceutical or biotechnology industry.
- Proven expertise in designing and managing clinical trials for specific therapeutic areas.
- Strong understanding of drug development processes, regulatory requirements (FDA, EMA, etc.), and Good Clinical Practice (GCP).
- Excellent scientific writing and presentation skills.
- Ability to think critically and strategically, with strong analytical and problem-solving capabilities.
- Effective interpersonal and communication skills, with the ability to influence and collaborate across diverse teams.
- Experience in (mention a specific therapeutic area, e.g., oncology, immunology, cardiovascular) is highly desirable.
- Proficiency in data analysis and interpretation, and experience with clinical data review.
This is an exciting opportunity to contribute to cutting-edge pharmaceutical research and development within a supportive and innovative environment. The hybrid working arrangement allows for a balance between focused individual work and collaborative team engagement at our **Coventry** facilities.
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