105 Clinical Trials jobs in the United Kingdom

Study Participant Recruiter

Belfast, Northern Ireland Celerion

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Study Participant Representative Belfast, Northern Ireland Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Celerion offers one of the most experienced clinical pharmacology research networks in the industry. Do you enjoy providing excellent customer service? If so, we may have the position for you! Celerion is currently seeking a full-time Study Participant Representative to join our clinical study recruitment team. In this role, you will answer inbound calls from the public interested in information regarding clinical study participation. You will screen callers and recruit those who meet eligibility criteria to participate in clinical studies. You will also be responsible for collecting and entering participant medical history information into our database system and make outbound calls to study participants as needed. We need candidates with the ability to work a flexible schedule and this will include mainly daytime shifts but occasionally evening or weekend shifts as well on a rotating basis. Requirements Must demonstrate excellent professional telephone communication skills Must demonstrate commitment to providing outstanding customer service Be able to sort information from multiple clinical studies and advise participants appropriately Computer data entry experience preferred Accuracy and attention to detail essential Proactive attitude Previous call centre, telemarketing, or promotional experience highly desirable Previous knowledge of medical terminology is preferred A-level education standard required Celerion Values: Integrity,Trust ,Teamwork, Respect Celerion is an Equal Opportunity Employer. Skills: Customer Service41bf1e1f-b16b-4260-a40a-17c77a06fd15
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Manager, Global Submission Management, Clinical Trials

Uxbridge, London Bristol Myers Squibb

Posted 3 days ago

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**Working with Us**
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.
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Scientist - Injectable Drug Product Process Development

Slough, South East Hobson Prior

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 -

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Senior Pharmaceutical Research Scientist

CF10 1AA Cardiff, Wales £75000 Annually WhatJobs

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full-time
Our client, a leading biopharmaceutical company dedicated to discovering and developing life-saving therapies, is looking for a highly motivated Senior Pharmaceutical Research Scientist to join their innovative, fully remote research team. This role offers a significant opportunity to contribute to cutting-edge drug discovery and development programs from anywhere in the UK. You will be responsible for designing and executing complex experimental studies, analyzing data, and interpreting results to advance preclinical and clinical research initiatives. The ideal candidate will possess a PhD or Master's degree in Pharmacology, Biochemistry, Molecular Biology, or a related life science field, along with a proven track record in pharmaceutical research. Expertise in areas such as medicinal chemistry, assay development, target validation, or specific therapeutic areas (e.g., oncology, immunology) is highly desirable. You will collaborate closely with cross-functional teams, including chemists, biologists, and clinicians, to drive projects forward. Key responsibilities include literature review, hypothesis generation, experimental design, data interpretation, and contributing to scientific publications and patent applications. Strong analytical skills, meticulous record-keeping, and excellent written and verbal communication are essential. This fully remote position requires self-motivation, excellent time management, and the ability to work independently while maintaining strong collaborative ties with colleagues via digital platforms. You will play a vital role in shaping the future of medicine and making a tangible difference in patient lives.
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Senior Pharmaceutical Research Scientist

NR1 1 Norwich, Eastern £70000 Annually WhatJobs

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full-time
Our client, a pioneering pharmaceutical company, is seeking a highly experienced Senior Pharmaceutical Research Scientist to join their fully remote, cutting-edge research and development division. This critical role focuses on the discovery and development of novel drug candidates, contributing to our pipeline of innovative therapies. You will lead key research projects, design and execute complex experiments, and analyze data to advance drug discovery efforts. Responsibilities include identifying new therapeutic targets, developing and optimizing assay methodologies, and characterizing the efficacy and safety profiles of potential drug compounds. The Senior Pharmaceutical Research Scientist will collaborate closely with medicinal chemists, biologists, and pharmacologists to drive projects forward. A deep understanding of pharmacology, drug metabolism, pharmacokinetics (DMPK), or related disciplines is essential. Experience with various in vitro and in vivo preclinical models, as well as expertise in specific therapeutic areas (e.g., oncology, immunology, neuroscience), is highly desirable. You will be responsible for interpreting complex scientific data, preparing detailed research reports, and contributing to regulatory submissions. Mentoring junior scientists, staying abreast of the latest scientific literature, and contributing to intellectual property strategies are also key aspects of this role. Key duties will include:
  • 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
A Ph.D. in Pharmacology, Pharmaceutical Sciences, Biochemistry, or a related life science field is required, along with a minimum of 6-8 years of relevant research experience in the pharmaceutical or biotechnology industry. A strong track record of contributing to drug discovery programs and a solid understanding of drug development processes are essential. Excellent communication, presentation, and data analysis skills are paramount. This remote position offers an exceptional opportunity to make a significant impact on the development of life-changing medicines.
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Principal Pharmaceutical Research Scientist

LS1 1AA Leeds, Yorkshire and the Humber £70000 Annually WhatJobs

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full-time
Our client, a globally recognised leader in pharmaceutical innovation, is looking for a highly accomplished Principal Pharmaceutical Research Scientist to join their cutting-edge, fully remote R&D team. This senior position offers an unparalleled opportunity to lead groundbreaking research initiatives and contribute significantly to the development of novel therapeutics. You will be instrumental in designing and executing complex research projects, analysing experimental data, and translating findings into actionable strategies for drug discovery and development. Responsibilities include proposing innovative research directions, mentoring junior scientists, collaborating with cross-functional teams (including biology, chemistry, and clinical development), preparing high-quality research reports and publications, and staying at the forefront of scientific advancements in the pharmaceutical field. The ideal candidate will possess a deep and comprehensive understanding of drug discovery processes, medicinal chemistry, pharmacology, and relevant therapeutic areas. A strong track record of successful research outcomes, evidenced by publications in reputable journals and patent filings, is essential. Exceptional analytical, critical thinking, and problem-solving skills are required, along with the ability to lead complex scientific endeavours and inspire a team. This is a fully remote position, requiring a high degree of self-motivation, organisational prowess, and effective virtual communication skills. You will be expected to manage your research portfolio autonomously, ensuring timely delivery of milestones. Our client is committed to fostering a collaborative and intellectually stimulating remote work environment, offering resources and support for professional growth. The role is anchored to Leeds, West Yorkshire, UK , but the position is 100% remote.

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.
If you are a visionary scientist seeking to make a significant impact in pharmaceutical R&D, this fully remote role offers an exceptional platform for your expertise and ambition.
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Senior Pharmaceutical Research Scientist

RG1 1AA Reading, South East £55000 Annually WhatJobs

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full-time
Our client is seeking a highly skilled and experienced Senior Pharmaceutical Research Scientist to join their innovative research and development team at their facility in Reading, Berkshire, UK . This role is critical to advancing our client's pipeline of novel therapeutics. The ideal candidate will have a strong background in drug discovery and development, with a proven track record of leading research projects and contributing to scientific publications.

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.
Qualifications:
  • 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.
This is an on-site role based at our client's cutting-edge facility in Reading, Berkshire, UK .
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Senior Pharmaceutical Research Scientist

B1 1BB Birmingham, West Midlands £65000 Annually WhatJobs

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full-time
Our client, a leading pharmaceutical company, is seeking a highly skilled and motivated Senior Pharmaceutical Research Scientist to join their cutting-edge R&D department in **Birmingham, West Midlands, UK**. This role is pivotal in driving the discovery and development of novel therapeutic agents. You will be responsible for designing and executing complex experiments, analysing data, and contributing to the intellectual property strategy within your area of expertise. The ideal candidate will have a strong background in drug discovery, medicinal chemistry, pharmacology, or a related field, with a proven track record of successfully advancing projects from early discovery through to pre-clinical development. Your responsibilities will include planning and conducting in vitro and in vivo studies, optimising lead compounds, and investigating mechanisms of action. You will work collaboratively with multidisciplinary teams, including biologists, chemists, pharmacologists, and toxicologists, to achieve project milestones. Essential skills include a deep understanding of experimental design, data interpretation, and the ability to critically evaluate scientific literature. Proficiency in relevant laboratory techniques, analytical instrumentation, and data analysis software is required. Experience with specific therapeutic areas such as oncology, immunology, or neuroscience would be a significant advantage. The role also involves presenting research findings at internal meetings and potentially at external scientific conferences, as well as contributing to the writing of regulatory documents. We are looking for a proactive, innovative scientist with excellent problem-solving skills and a commitment to scientific excellence. This is an outstanding opportunity to contribute to the development of life-changing medicines within a dynamic and supportive research environment.

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.
Qualifications:
  • 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

NE1 5XU Newcastle upon Tyne, North East £65000 Annually WhatJobs

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full-time
Our client is a leading innovator in the pharmaceutical sector, seeking a highly motivated and experienced Senior Pharmaceutical Research Scientist to join their dynamic, remote-first team. This role is pivotal in driving forward groundbreaking research and development initiatives, contributing to the creation of novel therapeutics that address unmet medical needs. You will be instrumental in designing, executing, and interpreting complex experiments, utilizing your expertise in medicinal chemistry, drug discovery, and preclinical development. The successful candidate will manage multiple projects concurrently, ensuring timely delivery of high-quality data and results. Key responsibilities include the synthesis and characterization of small molecules, the evaluation of their biological activity in vitro and in vivo, and the identification of promising drug candidates. You will also be responsible for staying abreast of the latest scientific literature and technological advancements in the field. Collaboration is key, and you will work closely with cross-functional teams including biologists, pharmacologists, and toxicologists, providing critical scientific input. While this role is fully remote, a strong commitment to communication, collaboration, and documentation is essential. You will maintain meticulous records, prepare scientific reports, and contribute to patent filings and regulatory submissions. The ideal candidate possesses a PhD in Organic Chemistry, Medicinal Chemistry, or a closely related field, with a proven track record of successful drug discovery projects. A minimum of 5 years of postdoctoral or industry experience is required. Excellent problem-solving skills, a strong understanding of ADME/Tox principles, and proficiency in modern analytical techniques (NMR, MS, HPLC) are expected. Experience with computational chemistry tools and structure-based drug design is a plus. This is an exceptional opportunity to make a significant impact on patient lives from the comfort of your home. The role is based in Newcastle upon Tyne, Tyne and Wear, UK , but is conducted entirely remotely.
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Senior Pharmaceutical Research Scientist

B1 1AA Birmingham, West Midlands £60000 Annually WhatJobs

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full-time
Our client, a leading pharmaceutical company committed to groundbreaking medical advancements, is seeking a highly accomplished Senior Pharmaceutical Research Scientist to join their esteemed R&D team in Birmingham, West Midlands, UK . This vital role involves leading complex research projects, driving drug discovery initiatives, and contributing to the development of innovative pharmaceutical products. You will be essential in advancing therapeutic solutions and improving patient outcomes.

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.
Qualifications:
  • 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.
This hybrid role offers a compelling opportunity to contribute to life-changing medicines in Birmingham.
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Senior Pharmaceutical Research Scientist

BN1 1AA East Sussex, South East £70000 Annually WhatJobs

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full-time
Our client is a leading pharmaceutical company looking for an exceptional Senior Pharmaceutical Research Scientist to join their cutting-edge research and development team in Brighton, East Sussex, UK . This role is critical to our client's mission of discovering and developing innovative therapeutic solutions. You will be responsible for designing and executing complex experiments, analyzing data, and contributing to the progression of drug candidates through the pipeline. This is a laboratory-based position that requires hands-on expertise and a deep understanding of pharmaceutical sciences.

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.
Qualifications and Skills:
  • 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.
This is a vital role within a dynamic pharmaceutical company, offering significant opportunities for professional growth and the chance to contribute to life-changing medicines. If you are a dedicated and accomplished scientist eager to make a difference, we encourage you to apply.
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  58. person_search Recruitment Consultancy
  59. store Retail
  60. point_of_sale Sales
  61. science Scientific Research & Development
  62. wifi Telecoms
  63. psychology Therapy
  64. pets Veterinary
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