105 Clinical Trials jobs in the United Kingdom
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Manager, Global Submission Management, Clinical Trials

Posted 3 days ago
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Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
**Position Purpose**
The Submission Manager, Clinical Trials manages and coordinates the timely, compliant, and accurate delivery of the core submission documents and dossiers to Bristol Myers Squibb (BMS) HA/EC Applicants and CRO. The Submission Manager also participates in the preparation of the CTIS for CT under the EU Regulation
**Key Responsibilities**
+ Prepare and distribute the global Clinical Trial Application dossier and subsequent substantial amendments to country applicants and CROs for submission to ECs and HAs.
+ Prepare the data required in CTIS for global Clinical Trial Application dossiers and their subsequent substantial modifications.
+ Manage the CT Amendment log considering the EU Regulation and determine windows of opportunity for submissions, escalate within BMS
+ Provide support to the Submission Senior Manager/collaborate with the Submission Specialist in CTA preparation activities for initial filings and start up activities, protocol amendments, end of trials and CSR distributions.
+ Ensure consistency of the Clinical Trial application across projects, studies and countries.
+ Lead Program/Study level CTA Tracking Meetings, in preparation of the CTA dossier, ensuring timelines and dossier quality are managed according to expectations.
+ Liaise with country offices and central team (Clinical Supply Operations, Operation Leads, Protocol Managers, Medical Monitor, Safety, Quality Person) to ensure that Clinical trial application activities are in compliance with study timelines, BMS SOPs, worldwide regulatory guidelines and regulations.
+ Comply with the use and maintenance of the available planning & tracking tools (e.g. Veeva - HA submission and approval Tracking system) to generate reports and track the CTA content and associated dates.
+ Escalate to study teams and GSM-CT senior roles observed trends and issues that may impact timely and successful study approval and execution
+ Contribute to the Global Country Requirements Repository by collecting and sharing additional country requirements.
+ Support initiatives for innovation and simplification in the processes to improve the support to the study teams and GSM-CT.
+ Coordinate updates within a Program.
+ Support continuous improvement and compliance initiatives
+ Utilizes technology effectively to support the clinical trial application submission process. Proficient use of CTMS, Tracking systems, Excel trackers, to generate reports and track the CTAp content and associated dates
+ Contributes to other requirements as appropriate to allow proper functioning of the GSM-CT.
+ Support implementation of the EU CT REG Portal from Feb 2022.
+ Provide training/mentoring to the GSM-CT newcomers
**Required Qualifications & Experience**
+ BA/BS degree in a science or technology field, preferred
+ Extensive relevant regulatory submissions experience
**Key Competencies**
+ Expert knowledge of Regulatory Submissions and package content for non-US clinical trial applications to health authorities.
+ Assists in the development of short- and long-term goals for own workgroup in alignment with those of GSM and the R&D umbrella.
+ Resolves problems/difficulties with the assistance of senior team members.
+ Supports other functions as appropriate.
+ Independently facilitate compound/study team meetings.
+ Works Independently and collaborates with other functional areas.
#LI-Hybrid
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
**Uniquely Interesting Work, Life-changing Careers**
With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
**On-site Protocol**
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit careers.bms.com/ ( eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Bristol Myers Squibb is Disability Confident - Employer
A UK Government scheme
**Company:** Bristol-Myers Squibb
**Req Number:** R
**Updated:** :40:14.637 UTC
**Location:** Uxbridge-GB
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
Scientist - Injectable Drug Product Process Development
Posted today
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Help bring science to life and join a leading pharmaceutical company to play a key role in delivering impactful medicines that drives healthcare innovation!
Hobson Prior is seeking a Drug Product Development Specialist to join a dynamic team within Pharmaceutical Development Sciences. This role focuses on injectable drug product manufacturing processes, supporting clinical and regulatory activities. You will collaborate with internal teams and external partners to ensure the successful development and production of sterile drug products.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Develop and refine manufacturing processes for injectable drug products from early studies to regulatory approval.
- Select and define manufacturing parameters for clinical production.
- Collaborate with internal teams and external manufacturers to meet project goals.
- Conduct lab studies, analyse data, and document findings (e.g., filter selection, fill volume assessments, compatibility tests).
- Analyse manufacturing data to improve process understanding and performance.
- Perform risk assessments for manufacturing processes.
- Design processes for sterile injectable products in various forms (e.g., liquid, lyophilized powder, pre-filled syringes).
- Support clinical trial preparation and ensure timely production of stability and clinical batches.
- Assist in process validation and ensure compliance with quality standards and regulations.
- Contribute to regulatory submissions and respond to authority queries.
- Investigate and resolve quality-related issues, such as deviations or complaints.
- Facilitate knowledge transfer from late-phase development to commercial production.
- Help improve departmental processes and ways of working.
Key Skills and Requirements:
- Experience in developing or manufacturing liquid drug products in the pharmaceutical industry.
- Familiarity with biopharmaceuticals is a plus.
- Knowledge of aseptic manufacturing processes, including vial, cartridge, and pre-filled syringe filling, is advantageous.
- Understanding of sterile drug product development, including components, process transfer, scale-up, and optimization, is beneficial.
For more information, please contact Jessica Taylor.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -
Senior Pharmaceutical Research Scientist
Posted today
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Senior Pharmaceutical Research Scientist
Posted today
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- Designing and leading preclinical drug discovery research projects
- Identifying and validating novel drug targets and therapeutic strategies
- Developing and optimizing in vitro and in vivo assay systems
- Conducting comprehensive pharmacological and DMPK studies
- Characterizing the efficacy and safety of drug candidates
- Collaborating with multidisciplinary teams to advance drug development
- Analyzing and interpreting complex experimental data
- Preparing research reports, scientific publications, and regulatory documents
- Mentoring junior research staff and contributing to team development
- Staying current with scientific advancements in relevant therapeutic areas
Principal Pharmaceutical Research Scientist
Posted today
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Qualifications:
- PhD in Pharmaceutical Sciences, Chemistry, Biology, Pharmacology, or a related discipline.
- Minimum of 10 years of progressive experience in pharmaceutical research and development.
- Extensive experience in drug discovery and development, with a proven track record of leading successful projects.
- Expertise in one or more therapeutic areas relevant to our client's focus.
- Strong publication record in peer-reviewed journals and experience with patent applications.
- Exceptional scientific leadership, mentorship, and project management skills.
- Advanced knowledge of research methodologies, experimental design, and data analysis.
- Excellent written and verbal communication skills, with the ability to present complex scientific information effectively.
- Demonstrated ability to work independently and thrive in a remote research setting.
Senior Pharmaceutical Research Scientist
Posted today
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Responsibilities:
- Design and conduct complex experiments in areas such as medicinal chemistry, pharmacology, or drug metabolism.
- Lead research projects from initial concept through to proof-of-concept, managing timelines and resources effectively.
- Analyze and interpret experimental data, drawing conclusions and making recommendations for future research directions.
- Develop and validate new assays and methodologies to support drug discovery and characterization.
- Collaborate with cross-functional teams, including chemists, biologists, toxicologists, and clinicians, to advance drug candidates.
- Prepare scientific reports, manuscripts for publication, and presentations for internal and external stakeholders.
- Contribute to the intellectual property portfolio by identifying patentable inventions.
- Mentor junior scientists and contribute to the scientific development of the team.
- Stay current with the latest scientific literature, technologies, and regulatory guidelines in the pharmaceutical industry.
- Ensure all research activities are conducted in compliance with Good Laboratory Practice (GLP) and other relevant regulatory standards.
- Manage external collaborations with academic institutions and contract research organizations (CROs).
- Contribute to the strategic planning of R&D programs.
- Ph.D. in Pharmacology, Medicinal Chemistry, Biochemistry, or a related life science discipline.
- Minimum of 5 years of post-doctoral or industry research experience in pharmaceutical drug discovery.
- Demonstrated expertise in at least one area of drug discovery (e.g., target identification, lead optimization, preclinical development).
- Proven track record of successfully leading research projects and contributing to the progression of drug candidates.
- Strong publication record in peer-reviewed journals.
- Excellent understanding of experimental design, data analysis, and statistical interpretation.
- Experience with various laboratory techniques and instrumentation relevant to pharmaceutical research.
- Exceptional problem-solving skills and a rigorous scientific approach.
- Strong communication and presentation skills, with the ability to articulate complex scientific concepts clearly.
- Ability to work effectively in a team-oriented, collaborative environment.
- Experience with regulatory affairs and submission processes is a plus.
Senior Pharmaceutical Research Scientist
Posted today
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Key Responsibilities:
- Design and conduct advanced experiments to support drug discovery and development.
- Analyse and interpret complex scientific data, drawing meaningful conclusions.
- Optimise lead compounds and investigate mechanisms of action for therapeutic agents.
- Collaborate effectively with cross-functional R&D teams.
- Contribute to project strategy, intellectual property development, and regulatory submissions.
- Author scientific reports, publications, and presentations.
- Maintain high standards of laboratory practice and safety.
- Stay current with scientific advancements and emerging technologies in pharmaceutical research.
- PhD or MSc in Pharmacy, Chemistry, Biology, Pharmacology, or a related life science discipline.
- Significant post-doctoral or industry experience in pharmaceutical research and drug discovery.
- Proven expertise in relevant therapeutic areas and/or drug discovery disciplines.
- Strong hands-on experience with various laboratory techniques and analytical methods.
- Excellent data analysis, critical thinking, and problem-solving skills.
- Proficiency in scientific writing and presentation.
- Ability to work independently and contribute effectively within a team environment.
- Experience in (Specify Therapeutic Area, e.g., Oncology, CNS) is highly desirable.
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Senior Pharmaceutical Research Scientist
Posted today
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Senior Pharmaceutical Research Scientist
Posted today
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Responsibilities:
- Lead and conduct cutting-edge research in drug discovery and development, focusing on (specify therapeutic area, e.g., oncology, immunology, neuroscience).
- Design, execute, and optimize experimental protocols to investigate novel therapeutic targets and compounds.
- Analyze complex biological and chemical data, interpreting results to guide research direction.
- Develop and validate new assay methodologies and analytical techniques.
- Collaborate closely with cross-functional teams, including medicinal chemists, pharmacologists, and toxicologists.
- Manage research projects, ensuring timely completion within budget and scope.
- Prepare comprehensive research reports, publications, and patent applications.
- Present research findings at internal meetings and external scientific conferences.
- Mentor and guide junior scientists, fostering their technical and scientific development.
- Stay abreast of the latest scientific literature, emerging technologies, and industry trends in pharmaceutical research.
- Ensure strict adherence to Good Laboratory Practices (GLP) and all relevant safety regulations.
- Contribute to the strategic planning of the R&D pipeline.
- Evaluate and implement new technologies to enhance research capabilities.
- Troubleshoot experimental challenges and develop innovative solutions.
- Contribute to the overall scientific strategy and intellectual property development of the company.
- Ph.D. in Pharmaceutical Sciences, Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 5-7 years of post-doctoral or industry research experience in drug discovery and development.
- Proven track record of successfully leading research projects and delivering significant scientific contributions.
- Extensive hands-on experience in (mention specific techniques, e.g., cell-based assays, in vivo models, molecular biology techniques, analytical chemistry).
- Strong understanding of drug discovery processes, from target identification to preclinical development.
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency in data analysis software and scientific literature databases.
- Exceptional written and verbal communication skills, with the ability to present complex scientific information effectively.
- Demonstrated leadership and mentorship abilities.
- Ability to work independently and collaboratively in a team-oriented research environment.
- Experience with regulatory requirements for drug development is a plus.
- Strong publication record in peer-reviewed journals.
- Commitment to scientific excellence and ethical research practices.
- Adaptability and a passion for innovation in pharmaceutical science.
Senior Pharmaceutical Research Scientist
Posted today
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As a Senior Pharmaceutical Research Scientist, you will lead specific research projects, mentor junior scientists, and collaborate with cross-functional teams including medicinal chemistry, pharmacology, and toxicology. Your primary focus will be on hypothesis generation, experimental design, and the execution of in vitro and in vivo studies to evaluate drug efficacy, safety, and mechanisms of action. You will be expected to interpret complex datasets, draw sound conclusions, and present your findings clearly to internal stakeholders and at scientific conferences. Maintaining detailed laboratory notebooks, ensuring compliance with Good Laboratory Practice (GLP) and other regulatory guidelines, and contributing to the publication of research results are integral to this role. The successful candidate will possess a strong scientific background, excellent problem-solving skills, and a passion for advancing pharmaceutical innovation.
Key Responsibilities:
- Design, conduct, and optimize in vitro and/or in vivo experiments to assess drug candidates.
- Analyze and interpret complex experimental data, draw scientifically sound conclusions.
- Develop and validate new assays and experimental models relevant to therapeutic areas.
- Contribute to the generation of hypotheses and the design of research strategies.
- Lead assigned research projects from conception to completion.
- Mentor and guide junior research scientists, fostering their scientific development.
- Collaborate effectively with internal R&D teams and external partners.
- Prepare detailed research reports, technical documentation, and scientific publications.
- Present research findings at internal meetings and scientific conferences.
- Ensure strict adherence to GLP, safety protocols, and regulatory guidelines.
- Maintain accurate and up-to-date laboratory records and databases.
- Contribute to the intellectual property portfolio of the company.
- Ph.D. in Pharmacology, Molecular Biology, Biochemistry, or a related life science discipline.
- Minimum of 5-7 years of post-doctoral or industry research experience in the pharmaceutical or biotechnology sector.
- Proven track record in designing and executing sophisticated experimental studies.
- Extensive experience in a specific therapeutic area (e.g., oncology, immunology, neuroscience) is highly desirable.
- Expertise in relevant experimental techniques (e.g., cell culture, molecular biology assays, animal models).
- Strong analytical and critical thinking skills.
- Excellent written and verbal communication skills.
- Ability to work effectively in a team-oriented, fast-paced environment.
- Experience with data analysis software and statistical methods.
- A strong commitment to scientific integrity and ethical research practices.