36 Principal Investigators jobs in the United Kingdom
Remote Scientific Research Lead - Bioinformatics
Posted 4 days ago
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Job Description
Key responsibilities include overseeing data analysis workflows, interpreting results, and translating complex biological findings into clear, actionable insights. The Research Lead will manage computational resources, ensure data integrity, and implement rigorous quality control measures. A significant part of the role involves collaborating with a geographically dispersed team of biologists, clinicians, and data scientists through virtual communication channels. You will also be responsible for staying abreast of the latest advancements in bioinformatics, computational biology, and relevant 'omics' technologies, and actively contributing to scientific publications and conference presentations. The ability to mentor junior researchers and provide technical guidance in a remote setting is essential. This role offers the unique advantage of a fully remote work environment, empowering you to work from anywhere while contributing to world-class scientific endeavors. The position requires a self-disciplined individual with exceptional project management skills and a proven ability to deliver high-impact research outcomes independently.
Key Responsibilities:
- Lead the design and execution of complex bioinformatics research projects.
- Develop and implement advanced computational methods and pipelines for 'omics' data analysis.
- Analyze large-scale genomic, transcriptomic, and proteomic datasets.
- Interpret biological findings and translate them into research insights.
- Ensure data quality, integrity, and robust statistical analysis.
- Collaborate effectively with remote scientific teams and stakeholders.
- Manage computational resources and optimize analysis workflows.
- Contribute to scientific publications, grant proposals, and presentations.
- Mentor and guide junior bioinformatics researchers.
- Stay current with cutting-edge bioinformatics tools and techniques.
- Ph.D. in Bioinformatics, Computational Biology, Computer Science, Statistics, or a related field.
- Minimum of 8 years of post-doctoral research experience in bioinformatics.
- Extensive experience with various 'omics' data types and analysis pipelines.
- Proficiency in programming languages such as Python and R, and strong command-line skills.
- Expertise in statistical analysis and machine learning methods relevant to biological data.
- Demonstrated track record of high-impact scientific publications.
- Proven ability to lead research projects and work independently in a remote setting.
- Excellent communication, collaboration, and problem-solving skills.
Senior Scientific Research Associate - Biotechnology
Posted 4 days ago
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Job Description
Responsibilities:
- Design, perform, and optimize complex experiments in molecular biology and biochemistry.
- Develop and validate new assays and experimental protocols.
- Analyze experimental data using appropriate statistical methods and software.
- Troubleshoot experimental issues and identify solutions.
- Accurately record and meticulously document all experimental procedures and results in electronic lab notebooks.
- Collaborate with project teams, present findings, and contribute to research strategy discussions.
- Maintain laboratory equipment and ensure compliance with safety regulations.
- Stay updated on relevant scientific literature and emerging technologies.
- Contribute to manuscript preparation and patent applications as needed.
- MSc or PhD in Molecular Biology, Biochemistry, Biotechnology, or a related life science discipline.
- Minimum of 5 years of post-graduate research experience in an industrial or academic R&D setting.
- Proven expertise in cell-based assays, molecular cloning, protein expression and purification, or similar relevant techniques.
- Strong understanding of drug discovery and development processes.
- Proficiency in data analysis software (e.g., GraphPad Prism, R).
- Excellent laboratory technique, attention to detail, and record-keeping skills.
- Strong written and verbal communication abilities.
- Ability to work independently and as part of a collaborative team.
- Experience with high-throughput screening (HTS) is a plus.
Principal Investigator
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Principal Investigator
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Principal Investigator
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Principal Investigator
Posted today
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Job Description
Principal Investigator (PI) – Clinical Research Site Network - Multiple Locations
We are seeking experienced Principal Investigators (PIs) to join a brand new fast-growing clinical research site network across the UK and US. This is a chance to be part of an innovative organisation transforming trial delivery with modern infrastructure, operational excellence, and a collaborative investigator community.
As a PI, you will oversee clinical trials at your site, ensuring patient safety, data integrity, and regulatory compliance , supported by dedicated operations teams and a strong pipeline of diverse studies.
What It’s Like to Work Here
- Join a growing network committed to expanding patient access to research.
- Focus on science and patient care while we handle operations and compliance.
- Collaborate with leading investigators across multiple therapeutic areas.
- Access a steady stream of high-quality, industry-sponsored trials .
Responsibilities
- Provide medical leadership for trials and safeguard participant well-being.
- Ensure compliance with ICH-GCP, FDA, EMA/MHRA regulations .
- Supervise sub-investigators and site staff.
- Oversee accurate documentation, reporting, and regulatory submissions.
Qualifications
- Medical Degree (MD, DO, MBBS, or equivalent ) with active license.
- Prior clinical research experience (PI or Sub-Investigator).
- GCP certification and strong leadership skills.
What We Offer
- Competitive compensation with performance incentives.
- Centralised support in operations, regulatory, and recruitment .
- Opportunities to grow your research portfolio and shape the future of clinical trials.
Principal Investigator
Posted today
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Job Description
We’re working with a leading, fully integrated Clinical Research Organization (CRO) in England, dedicated to advancing innovative medical treatments through exceptional patient care and the delivery of high-quality clinical data.
I’m currently partnering with several top-5 global pharmaceutical companies to identify an
experienced Principal Investigator for a high-profile clinical research program.
They are seeking an experienced Principal Investigator (PI) to join their expert team.
In this role, you will:
- Provide medical leadership and oversight across multiple clinical trials
- Ensure participant safety, regulatory compliance, and GCP adherence
- Collaborate closely with sponsors, CRO teams, and regulatory authorities
- Contribute to cutting-edge research that impacts global healthcare
What we’re looking for:
- Licensed physician (MD or equivalent)
- Proven experience as a Principal Investigator or Sub-Investigator
- Strong knowledge of clinical trial processes, GCP, and regulatory standards
- Passion for advancing medical innovation through clinical research
This is a fantastic opportunity to join a respected CRO at the forefront of clinical development.
Why Join Us?
- Opportunity to lead groundbreaking clinical research in a dynamic environment
- Competitive freelance/consulting terms
- Work with a dedicated team committed to scientific excellence and innovation
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Principal Investigator
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Principal Investigator – Clinical Development (Contract)
Location: London, UK
Employment type: Contract / Freelance ~ 12-16 month contract (possibility of extension)
We are seeking a highly skilled and motivated Principal Investigator (PI) to join a leading clinical research organization dedicated to advancing innovative medical treatments. This role offers the opportunity to be at the forefront of clinical development, working alongside an experienced research team to deliver high-quality data and exemplary patient care.
As a Principal Investigator, you will be entrusted with the conduct, oversight, and medical leadership of clinical trials at a site level. You will play a pivotal role in ensuring participant safety, maintaining compliance with Good Clinical Practice (GCP) guidelines, and driving the successful execution of studies. This position is ideal for physicians, scientists and pharmacists with a passion for clinical research who want to contribute directly to the progress of new therapies that have the potential to improve patient outcomes worldwide.
Key Responsibilities:
- Provide overall medical leadership and direction for assigned studies, ensuring strict adherence to study protocols and regulatory requirements.
- Safeguard the rights, safety, and well-being of all trial participants.
- Evaluate participant eligibility, conduct physical assessments, and perform study-specific procedures.
- Review and interpret diagnostic data, including lab work, ECGs, and imaging, as required.
- Oversee the administration of investigational products and ensure compliance with study protocols.
- Maintain accurate, complete, and timely documentation of study data and source records.
- Act as primary liaison with sponsors, monitors, and regulatory bodies, participating in audits and inspections as required.
- Report adverse events promptly in compliance with study-specific and regulatory reporting requirements.
- Provide scientific and medical input for new study feasibility assessments.
- Guide and support clinical research staff to ensure quality standards are consistently met.
Qualifications:
- M.D. or D.O. with active, unrestricted medical license in the state where research will be conducted.
- Board certification (or board eligibility) in a relevant specialty.
- Training and certification in Good Clinical Practice (GCP).
- Strong knowledge of clinical trial protocols, regulatory requirements, and biomedical research ethics.
- Excellent communication skills with the ability to collaborate cross-functionally.
- Demonstrated ability to critically evaluate clinical data and resolve challenges with sound judgment.
- Willingness to travel occasionally (up to 10%) for sponsor meetings, trainings, or professional conferences.
Tangible Benefits:
- Competitive compensation package with performance-based incentives.
- Medical, dental, and vision coverage.
- Retirement savings plan with employer contributions.
- Generous paid time off and recognized company holidays.
- Ongoing opportunities for career development, training, and advancement within clinical research.
Principal Investigator
Posted today
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Job Description
Principal Investigator (PI) – Clinical Research Site Network - Multiple Locations
Find out exactly what skills, experience, and qualifications you will need to succeed in this role before applying below.We are seeking experienced Principal Investigators (PIs) to join a brand new fast-growing clinical research site network across the UK and US. This is a chance to be part of an innovative organisation transforming trial delivery with modern infrastructure, operational excellence, and a collaborative investigator community.
As a PI, you will oversee clinical trials at your site, ensuring patient safety, data integrity, and regulatory compliance, supported by dedicated operations teams and a strong pipeline of diverse studies.
What It’s Like to Work Here
- Join a growing network committed to expanding patient access to research.
- Focus on science and patient care while we handle operations and compliance.
- Collaborate with leading investigators across multiple therapeutic areas.
- Access a steady stream of high-quality, industry-sponsored trials.
Responsibilities
- Provide medical leadership for trials and safeguard participant well-being.
- Ensure compliance with ICH-GCP, FDA, EMA/MHRA regulations.
- Supervise sub-investigators and site staff.
- Oversee accurate documentation, reporting, and regulatory submissions.
Qualifications
- Medical Degree (MD, DO, MBBS, or equivalent) with active license.
- Prior clinical research experience (PI or Sub-Investigator).
- GCP certification and strong leadership skills.
What We Offer
- Competitive compensation with performance incentives.
- Centralised support in operations, regulatory, and recruitment.
- Opportunities to grow your research portfolio and shape the future of clinical trials.
Principal Investigator
Posted today
Job Viewed
Job Description
We’re working with a leading, fully integrated Clinical Research Organization (CRO) in England, dedicated to advancing innovative medical treatments through exceptional patient care and the delivery of high-quality clinical data.
Apply promptly! A high volume of applicants is expected for the role as detailed below, do not wait to send your CV.I’m currently partnering with several top-5 global pharmaceutical companies to identify an
experienced Principal Investigator for a high-profile clinical research program.
They are seeking an experienced Principal Investigator (PI) to join their expert team.
In this role, you will:
- Provide medical leadership and oversight across multiple clinical trials
- Ensure participant safety, regulatory compliance, and GCP adherence
- Collaborate closely with sponsors, CRO teams, and regulatory authorities
- Contribute to cutting-edge research that impacts global healthcare
What we’re looking for:
- Licensed physician (MD or equivalent)
- Proven experience as a Principal Investigator or Sub-Investigator
- Strong knowledge of clinical trial processes, GCP, and regulatory standards
- Passion for advancing medical innovation through clinical research
This is a fantastic opportunity to join a respected CRO at the forefront of clinical development.
Why Join Us?
- Opportunity to lead groundbreaking clinical research in a dynamic environment
- Competitive freelance/consulting terms
- Work with a dedicated team committed to scientific excellence and innovation