2,166 Pharmacologist jobs in the United Kingdom
Senior Clinical Pharmacologist
SO14 1AA Southampton, South East
£60000 Annually
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly accomplished Senior Clinical Pharmacologist to join their dynamic, fully remote research and development team. This critical role focuses on the design, execution, and interpretation of clinical pharmacology studies to support the development of innovative medicines. You will play a key role in characterizing drug safety and efficacy profiles, contributing significantly to regulatory submissions. As a fully remote position, this role offers the flexibility to work from anywhere in the UK, fostering a healthy work-life balance. The ideal candidate will possess a strong scientific background, extensive experience in clinical drug development, and a commitment to advancing pharmaceutical science.
Key Responsibilities:
Qualifications:
This fully remote position offers an unparalleled opportunity for a leading clinical pharmacologist to contribute to groundbreaking pharmaceutical innovation. If you are driven by scientific excellence and seek a flexible, remote career, we encourage you to apply and join our client's world-class team, making an impact from anywhere, including the vicinity of Southampton, Hampshire, UK .
Key Responsibilities:
- Design and develop clinical pharmacology study protocols, including Phase I-IV studies.
- Oversee the execution of clinical pharmacology studies, ensuring adherence to scientific standards and regulatory guidelines.
- Analyze and interpret complex pharmacokinetic (PK) and pharmacodynamic (PD) data.
- Develop PK/PD models to characterize drug behavior and predict clinical outcomes.
- Prepare high-quality study reports, regulatory submission documents, and scientific publications.
- Collaborate with cross-functional teams, including R&D, regulatory affairs, medical affairs, and biostatistics.
- Provide scientific expertise on drug development strategies and clinical pharmacology principles.
- Stay abreast of the latest advancements in clinical pharmacology, drug metabolism, and pharmacogenomics.
- Mentor and guide junior scientists and research associates.
- Contribute to the strategic direction of the drug development pipeline.
Qualifications:
- Ph.D. or Pharm.D. in Pharmacology, Clinical Pharmacology, Pharmaceutical Sciences, or a related discipline.
- A minimum of 7 years of experience in clinical pharmacology within the pharmaceutical or biotechnology industry.
- Proven experience in designing, conducting, and analyzing PK/PD studies.
- In-depth knowledge of drug development processes and regulatory requirements (FDA, EMA).
- Expertise in pharmacokinetic/pharmacodynamic modeling and simulation software (e.g., NONMEM, Phoenix WinNonlin).
- Strong analytical, statistical, and problem-solving skills.
- Excellent written and verbal communication skills, with the ability to present complex scientific information effectively.
- Demonstrated ability to work independently and collaboratively in a remote team environment.
- A proactive approach and a passion for contributing to the development of new therapies.
- Experience with oncology or other therapeutic areas is a plus.
This fully remote position offers an unparalleled opportunity for a leading clinical pharmacologist to contribute to groundbreaking pharmaceutical innovation. If you are driven by scientific excellence and seek a flexible, remote career, we encourage you to apply and join our client's world-class team, making an impact from anywhere, including the vicinity of Southampton, Hampshire, UK .
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0
Senior Pharmacologist (Remote)
EH1 2HQ Edinburgh, Scotland
£75000 Annually
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Posted 20 days ago
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Job Description
Our client, a renowned pharmaceutical company, is seeking an accomplished Senior Pharmacologist to contribute to their cutting-edge drug development programs. This is a fully remote position, offering a flexible and stimulating work environment for an expert based anywhere in the UK. The Senior Pharmacologist will be pivotal in investigating the mechanisms of drug action, assessing efficacy and safety profiles, and driving preclinical research forward. You will be an integral part of a globally distributed research team, utilizing your extensive knowledge to shape the future of medicine.
Responsibilities:
Responsibilities:
- Design, execute, and interpret complex pharmacological studies in vitro and in vivo.
- Investigate drug mechanisms of action and explore potential therapeutic applications.
- Develop and validate novel pharmacological assays to assess drug efficacy and safety.
- Collaborate with medicinal chemists, toxicologists, and other research scientists to advance drug candidates.
- Analyze and interpret complex datasets, employing statistical methods and generating clear, concise reports.
- Contribute to the preparation of regulatory submissions and scientific publications.
- Stay current with the latest advancements in pharmacology and related fields.
- Provide expert advice on study design and interpretation of results to research teams.
- Mentor junior scientists and contribute to the scientific culture of the organization.
- Ensure all research activities are conducted in compliance with ethical guidelines and regulatory standards.
- Ph.D. in Pharmacology, Toxicology, or a related biomedical science discipline.
- Minimum of 6 years of relevant research experience in the pharmaceutical or biotechnology industry.
- Proven expertise in a variety of in vitro and in vivo pharmacological models.
- Strong understanding of pharmacokinetics (PK) and pharmacodynamics (PD) principles.
- Experience with data analysis software (e.g., R, SPSS, GraphPad Prism) and statistical methodologies.
- Excellent scientific writing and presentation skills, with a record of peer-reviewed publications.
- Demonstrated ability to independently design, conduct, and manage research projects.
- Experience in a remote work setting and proficiency with virtual collaboration tools.
- A strong commitment to scientific rigor and innovation in drug discovery.
- Ability to critically evaluate scientific literature and identify strategic research opportunities.
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1
Senior Pharmacologist - Drug Discovery
ST1 2NU Staffordshire, West Midlands
£70000 Annually
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Posted 3 days ago
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Job Description
Our client is at the forefront of pharmaceutical innovation and is seeking a highly skilled Senior Pharmacologist to join their dedicated drug discovery team. This is a fully remote position, offering the flexibility to work from anywhere within the UK, contributing to critical research from the comfort of your home office. You will play a pivotal role in identifying and validating novel drug targets, designing and conducting preclinical studies, and contributing to the advancement of therapeutic candidates from early discovery through to clinical development. Your expertise will be crucial in shaping the company's pipeline and driving impactful breakthroughs.
Key responsibilities will encompass:
The ideal candidate will hold a PhD in Pharmacology, Toxicology, or a closely related life science discipline, with a minimum of 5-7 years of post-doctoral or industry experience in drug discovery. A deep understanding of pharmacokinetic (PK) and pharmacodynamic (PD) principles is essential. Demonstrated experience with a range of in vitro and in vivo pharmacological techniques relevant to specific therapeutic areas (e.g., oncology, immunology, neuroscience) is highly desirable. Proficiency in data analysis software (e.g., GraphPad Prism, R) and a strong understanding of statistical methods are required. Excellent written and verbal communication skills are necessary for effective scientific reporting and collaboration. The ability to work independently, manage multiple projects simultaneously, and thrive in a remote team setting is crucial. Experience with regulatory submissions (e.g., IND, NDA) is a significant advantage. This role offers a unique opportunity to make a substantial impact on the development of life-changing medicines.
Key responsibilities will encompass:
- Designing, executing, and interpreting in vitro and in vivo pharmacological studies to assess the efficacy and safety of potential drug candidates.
- Developing and validating novel assays for target engagement, mechanism of action, and pharmacokinetic profiling.
- Collaborating closely with medicinal chemists, biologists, and other research scientists to integrate pharmacological data into drug design strategies.
- Analyzing complex experimental data, troubleshooting assays, and ensuring the highest standards of scientific rigor.
- Contributing to the strategic planning and prioritization of drug discovery projects.
- Writing comprehensive study reports, research summaries, and contributing to the preparation of regulatory documents.
- Keeping abreast of the latest scientific literature, industry trends, and technological advancements in pharmacology and related fields.
- Presenting research findings at internal team meetings and external scientific conferences.
- Mentoring junior scientists and contributing to a collaborative and innovative research environment.
- Ensuring all research activities are conducted in compliance with relevant ethical guidelines and regulatory standards.
- Managing external collaborations and contract research organizations (CROs) as needed.
The ideal candidate will hold a PhD in Pharmacology, Toxicology, or a closely related life science discipline, with a minimum of 5-7 years of post-doctoral or industry experience in drug discovery. A deep understanding of pharmacokinetic (PK) and pharmacodynamic (PD) principles is essential. Demonstrated experience with a range of in vitro and in vivo pharmacological techniques relevant to specific therapeutic areas (e.g., oncology, immunology, neuroscience) is highly desirable. Proficiency in data analysis software (e.g., GraphPad Prism, R) and a strong understanding of statistical methods are required. Excellent written and verbal communication skills are necessary for effective scientific reporting and collaboration. The ability to work independently, manage multiple projects simultaneously, and thrive in a remote team setting is crucial. Experience with regulatory submissions (e.g., IND, NDA) is a significant advantage. This role offers a unique opportunity to make a substantial impact on the development of life-changing medicines.
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Senior Clinical Pharmacologist - Remote
G1 1AA Glasgow, Scotland
£80000 Annually
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Posted 4 days ago
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Job Description
Our client, a globally recognized pharmaceutical leader dedicated to advancing healthcare through innovative medicines, is seeking a highly accomplished Senior Clinical Pharmacologist to join their expanding research division. This position is fully remote, offering exceptional flexibility for candidates across the UK. You will play a pivotal role in the design, execution, and interpretation of clinical pharmacology studies for novel drug candidates, contributing significantly to the development of life-saving therapies. The ideal candidate will possess extensive expertise in clinical pharmacology, pharmacokinetics (PK), pharmacodynamics (PD), and drug metabolism, with a proven track record in managing and leading clinical pharmacology programs from early phase through to registration.
As a Senior Clinical Pharmacologist, your responsibilities will include developing clinical pharmacology strategies, authoring study protocols, statistical analysis plans, and clinical study reports. You will collaborate closely with cross-functional teams, including clinical development, regulatory affairs, biostatistics, and project management, to ensure the successful and timely execution of studies. Strong understanding of regulatory guidelines (ICH, FDA, EMA) and their application in clinical pharmacology is essential. You will be expected to present complex scientific data to internal stakeholders, regulatory agencies, and at scientific conferences. The ability to critically evaluate data, identify potential risks and opportunities, and make informed recommendations regarding drug development pathways is paramount. This role requires excellent scientific judgment, strong leadership capabilities, and outstanding written and verbal communication skills. A commitment to scientific rigor and ethical conduct is fundamental.
Key Responsibilities:
As a Senior Clinical Pharmacologist, your responsibilities will include developing clinical pharmacology strategies, authoring study protocols, statistical analysis plans, and clinical study reports. You will collaborate closely with cross-functional teams, including clinical development, regulatory affairs, biostatistics, and project management, to ensure the successful and timely execution of studies. Strong understanding of regulatory guidelines (ICH, FDA, EMA) and their application in clinical pharmacology is essential. You will be expected to present complex scientific data to internal stakeholders, regulatory agencies, and at scientific conferences. The ability to critically evaluate data, identify potential risks and opportunities, and make informed recommendations regarding drug development pathways is paramount. This role requires excellent scientific judgment, strong leadership capabilities, and outstanding written and verbal communication skills. A commitment to scientific rigor and ethical conduct is fundamental.
Key Responsibilities:
- Develop and implement clinical pharmacology strategies for drug development programs.
- Design, write, and oversee clinical pharmacology studies (Phase I-IV).
- Analyze and interpret PK, PD, and drug metabolism data.
- Contribute to the development of regulatory submissions (e.g., IND, NDA).
- Collaborate with internal and external stakeholders, including CROs and regulatory agencies.
- Provide scientific and strategic input into drug development decisions.
- Author clinical pharmacology sections of regulatory documents and publications.
- Stay abreast of scientific advancements and regulatory changes in clinical pharmacology.
- Mentor junior scientists and contribute to team development.
- MD or PhD in Pharmacology, Clinical Pharmacology, or a related life sciences discipline.
- Minimum of 7 years of experience in clinical pharmacology within the pharmaceutical industry.
- Extensive experience with Phase I-IV clinical trials and PK/PD modeling.
- Deep understanding of regulatory guidelines and submission requirements.
- Excellent scientific writing and presentation skills.
- Proven ability to lead and collaborate effectively in a remote environment.
- Strong analytical and problem-solving capabilities.
- Eligibility to work remotely within the UK.
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3
Remote Senior Clinical Pharmacologist
WV1 1DU Wolverhampton, West Midlands
£70000 Annually
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Posted 10 days ago
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Job Description
Our client, a global pharmaceutical leader, is seeking a highly experienced Senior Clinical Pharmacologist to join their expanding team. This is a fully remote position, allowing you to contribute to groundbreaking research from anywhere in the UK. You will play a critical role in the design, execution, and interpretation of clinical pharmacology studies for novel drug candidates across various therapeutic areas. Responsibilities include developing study protocols, statistical analysis plans, and clinical study reports that meet regulatory requirements. You will contribute to regulatory submissions, interact with health authorities, and provide expert scientific advice on drug development strategies. This role requires a deep understanding of pharmacokinetics (PK), pharmacodynamics (PD), drug metabolism, and drug-drug interactions. You will collaborate closely with clinical development teams, statisticians, bioanalytical scientists, and regulatory affairs professionals. The ideal candidate will have a PhD or PharmD, with a strong background in clinical pharmacology and drug development. A minimum of 7 years of relevant industry experience is essential. Proven expertise in designing and conducting Phase I-III clinical trials, including first-in-human studies, is required. Excellent knowledge of ICH guidelines and global regulatory requirements (FDA, EMA) is mandatory. Strong analytical skills, proficiency in PK/PD modeling software (e.g., NONMEM, Phoenix WinNonlin), and the ability to interpret complex datasets are crucial. Exceptional written and verbal communication skills are needed to present findings and influence decision-making. This is an exceptional opportunity to drive the clinical pharmacology strategy for innovative medicines and contribute to improving patient outcomes. Our client offers a flexible, remote-first working environment, fostering collaboration and professional growth. Join a company dedicated to scientific excellence and making a difference in healthcare. The insights you provide will directly shape the future of our client's drug pipeline. Wolverhampton, West Midlands, UK .
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Senior Clinical Pharmacologist (Remote)
L3 4AB Liverpool, North West
£70000 Annually
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Posted 12 days ago
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Job Description
Our client, a leading pharmaceutical research and development organisation, is seeking a highly qualified Senior Clinical Pharmacologist to join their dedicated team on a fully remote basis. This vital role contributes to the design, execution, and interpretation of clinical pharmacology studies, ultimately shaping the development of innovative new medicines. You will leverage your deep expertise in pharmacokinetics (PK), pharmacodynamics (PD), and drug metabolism to provide critical insights and guidance throughout the drug development process. Working from your home office, you will collaborate virtually with scientists, clinicians, and regulatory affairs professionals to advance our pipeline.
Key responsibilities will include:
Key responsibilities will include:
- Designing clinical pharmacology studies (e.g., first-in-human, dose escalation, drug-drug interaction studies) in alignment with regulatory requirements and project objectives.
- Developing and reviewing study protocols, investigator brochures, and other regulatory submission documents.
- Interpreting PK/PD data, performing population PK analyses, and evaluating drug metabolism and pharmacokinetic variability.
- Contributing to the characterisation of the safety and efficacy profiles of investigational drugs.
- Providing scientific and technical expertise on clinical pharmacology aspects to cross-functional project teams.
- Developing strategies for dose selection and optimisation throughout the drug development lifecycle.
- Collaborating with biostatisticians and data managers to ensure the integrity and appropriate analysis of clinical pharmacology data.
- Interfacing with regulatory agencies (e.g., FDA, EMA) to present study designs and results.
- Mentoring junior scientists and contributing to the scientific development of the clinical pharmacology department.
- Staying abreast of the latest advancements in clinical pharmacology, modelling and simulation, and regulatory guidelines.
- Presenting scientific findings at internal meetings and external conferences.
- Ensuring all activities are conducted in compliance with GCP and relevant regulatory standards.
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5
Senior Clinical Pharmacologist (Remote)
L1 8JQ Liverpool, North West
£75000 Annually
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Posted 20 days ago
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Job Description
Our client, a pioneering global pharmaceutical company, is seeking a highly qualified Senior Clinical Pharmacologist to join their innovative research and development team on a fully remote basis. This crucial role involves designing, executing, and analyzing clinical pharmacology studies to support the development of novel therapeutics, all managed from your home office. You will be instrumental in defining the pharmacokinetic (PK) and pharmacodynamic (PD) profiles of investigational drugs, ensuring their safety and efficacy in human subjects. The ideal candidate will possess deep expertise in clinical pharmacology, drug metabolism, and pharmacokinetic/pharmacodynamic (PK/PD) modeling. Your responsibilities will include developing study protocols, overseeing data collection and analysis, and interpreting study results to guide clinical development decisions. You will collaborate closely with cross-functional teams, including clinical operations, biostatistics, and regulatory affairs, to ensure the successful progression of drug candidates through the development pipeline. Experience with NONMEM or other population PK/PD modeling software is essential. This is an outstanding opportunity to contribute to cutting-edge pharmaceutical research and development while enjoying the benefits of a remote work arrangement. We are looking for a scientific leader with strong analytical skills, excellent written and verbal communication abilities, and a comprehensive understanding of drug discovery and development processes. Your contributions will directly shape the future of medicine and improve patient outcomes.
Responsibilities:
Responsibilities:
- Design, develop, and execute clinical pharmacology studies.
- Analyze pharmacokinetic (PK) and pharmacodynamic (PD) data.
- Develop and apply population PK/PD models to characterize drug behavior.
- Interpret study results and provide recommendations for clinical development strategies.
- Collaborate with clinical teams, biostatisticians, and regulatory affairs.
- Prepare study protocols, analysis plans, and clinical study reports.
- Ensure compliance with regulatory guidelines and ethical standards.
- Stay abreast of scientific literature and advancements in clinical pharmacology.
- Mentor junior scientists and contribute to team development.
- PhD or PharmD in Pharmacology, Pharmaceutical Sciences, or a related discipline.
- Minimum of 7 years of experience in clinical pharmacology within the pharmaceutical industry.
- Extensive experience in designing and conducting Phase I-IV clinical pharmacology studies.
- Proficiency in population PK/PD modeling software (e.g., NONMEM, Phoenix WinNonlin).
- Strong understanding of drug metabolism, drug interactions, and bioanalytical methods.
- Excellent scientific writing and presentation skills.
- Ability to work independently and collaboratively in a remote environment.
- Knowledge of regulatory requirements (FDA, EMA) related to drug development.
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6
Pharmaceutical Research Scientist
MK40 1AA Milton Keynes, South East
£45000 Annually
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Posted 1 day ago
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Job Description
Our client, a leading innovator in the pharmaceutical industry, is seeking a highly skilled and dedicated Pharmaceutical Research Scientist to join their cutting-edge research and development team. This role is integral to the discovery and development of novel therapeutic compounds. You will be responsible for designing and conducting experiments, analyzing data, and contributing to the advancement of drug discovery pipelines. The ideal candidate will possess a strong academic background in a relevant scientific discipline, excellent laboratory skills, and a passion for scientific innovation. This is an on-site position, offering the opportunity to collaborate closely with a world-class research team.
Key Responsibilities:
Key Responsibilities:
- Design, execute, and optimize in vitro and in vivo experiments to evaluate drug candidates.
- Develop and validate new assays and methodologies for drug discovery and characterization.
- Analyze experimental data using statistical software and interpret results to guide research directions.
- Contribute to the preparation of scientific publications, patents, and regulatory submissions.
- Collaborate effectively with cross-functional teams, including medicinal chemistry, pharmacology, and toxicology.
- Maintain detailed and accurate laboratory notebooks and records.
- Stay abreast of the latest scientific literature and advancements in pharmaceutical research.
- Troubleshoot experimental challenges and propose innovative solutions.
- Participate in regular team meetings and present research findings.
- Ensure compliance with all laboratory safety procedures and ethical guidelines.
- Contribute to the overall strategic direction of drug discovery programs.
- Ph.D. or Master's degree in Pharmacology, Biochemistry, Molecular Biology, Chemistry, or a related life science field.
- Demonstrated experience in drug discovery or a related pharmaceutical research area.
- Proficiency in relevant experimental techniques (e.g., cell culture, molecular biology techniques, bioassays, chromatography).
- Strong analytical and data interpretation skills, with experience in statistical analysis software.
- Excellent written and verbal communication skills, with the ability to present complex scientific information clearly.
- Ability to work independently and as part of a collaborative research team.
- A strong publication record is a plus.
- Experience with specific therapeutic areas (e.g., oncology, immunology, neuroscience) is advantageous.
- Familiarity with regulatory guidelines (e.g., FDA, EMA) is desirable.
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7
Pharmaceutical Research Scientist
ST1 4AA Staffordshire, West Midlands
£50000 annum + ben
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Posted 1 day ago
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Job Description
Our client, a leading pharmaceutical research company, is actively seeking a talented and dedicated Pharmaceutical Research Scientist to join their innovative R&D team. This is a fully remote position, allowing exceptional scientists to contribute their expertise from anywhere in the UK. The successful candidate will play a pivotal role in the discovery and development of novel therapeutics. This involves designing and conducting experiments, analysing complex biological data, and contributing to the interpretation of research findings. You will be involved in various stages of the drug discovery pipeline, from target identification and validation to lead optimisation. A deep understanding of molecular biology, biochemistry, or pharmacology, coupled with hands-on laboratory experience, is crucial. The ability to critically evaluate scientific literature, propose innovative research ideas, and effectively communicate results to both scientific and non-scientific audiences is essential. This role demands meticulous attention to detail, strong problem-solving skills, and the capacity to work independently within a virtual research setting. Collaboration with external partners and internal multidisciplinary teams will also be a key aspect of this role.
Key Responsibilities:
Key Responsibilities:
- Design, execute, and optimise in vitro and in vivo experiments to investigate disease mechanisms and therapeutic targets.
- Perform detailed analysis and interpretation of experimental data using appropriate statistical methods.
- Contribute to the design and execution of drug discovery projects.
- Stay abreast of the latest scientific literature and technological advancements in the pharmaceutical field.
- Prepare clear and concise research reports, presentations, and publications.
- Collaborate effectively with colleagues across different scientific disciplines.
- Maintain high standards of laboratory practice and data integrity.
- Contribute to the intellectual property generation and patent filing process.
- Troubleshoot experimental procedures and propose alternative solutions.
- PhD in Pharmacology, Molecular Biology, Biochemistry, or a related life science discipline.
- Extensive hands-on experience in relevant experimental techniques (e.g., cell culture, molecular cloning, protein assays, animal models).
- Proven ability to design and execute complex research projects.
- Strong analytical and critical thinking skills.
- Excellent written and oral communication skills, with experience in scientific writing.
- Demonstrated ability to work independently and manage projects effectively in a remote environment.
- Experience with data analysis software (e.g., GraphPad Prism, R).
- Knowledge of drug discovery processes and regulatory requirements is a plus.
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8
Pharmaceutical Research Scientist
NR1 2AA Norwich, Eastern
£40000 Annually
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Posted 1 day ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly motivated Pharmaceutical Research Scientist to join their innovative R&D department in Norwich, Norfolk, UK . This role will involve conducting cutting-edge research to discover and develop new pharmaceutical compounds and therapies. You will be responsible for designing and executing complex experiments, analyzing experimental data, and contributing to the interpretation of results in the context of drug discovery programs. The ideal candidate will have a strong background in medicinal chemistry, pharmacology, or a related life science discipline, with hands-on experience in laboratory techniques relevant to drug discovery. You will work collaboratively within multidisciplinary teams, including chemists, biologists, and toxicologists, to advance projects from early-stage research through to preclinical development. Responsibilities include literature reviews, protocol development, synthesis and characterization of novel compounds, and in vitro/in vivo study design and execution. The ability to troubleshoot experimental challenges, maintain accurate laboratory records, and communicate findings effectively through presentations and written reports is essential. We are looking for a proactive scientist with excellent problem-solving skills and a commitment to scientific rigor and innovation. This role offers an exciting opportunity to contribute to the development of life-saving medicines and to work in a dynamic and collaborative research environment.
Responsibilities:
Responsibilities:
- Conduct research to identify and develop novel pharmaceutical compounds.
- Design and execute experiments in medicinal chemistry and pharmacology.
- Analyze and interpret complex experimental data.
- Synthesize and characterize new chemical entities.
- Perform in vitro and in vivo assays.
- Contribute to the design of drug discovery programs.
- Collaborate with cross-functional research teams.
- Maintain detailed laboratory notebooks and prepare research reports.
- Stay up-to-date with scientific literature and industry trends.
- Contribute to the optimization of synthetic routes and assay methodologies.
- PhD or Master's degree in Medicinal Chemistry, Pharmacology, Biochemistry, or a related field.
- Proven experience in pharmaceutical research and drug discovery.
- Hands-on experience with relevant laboratory techniques (e.g., organic synthesis, HTS, cell-based assays).
- Strong understanding of drug discovery principles and processes.
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency in data analysis software.
- Strong written and verbal communication skills.
- Ability to work effectively in a team-oriented research environment.
- Experience with literature databases (e.g., SciFinder, PubMed).
- Commitment to laboratory safety and compliance.
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