5 Clinical Laboratory Scientists jobs in London

ARTO is currently partnered with a Global Pharmaceutical company who are looking at a period of sustained growth after a recent approval at the proof of concept phase. Their therapeutic focus spans Neuroscience, Immunology (Dermatology) and also Oncology, with assets both in early and late phase development.

We are seeking an experienced Clinical Scientist (Associate Director level) to join our neuroscience team and contribute to the design and execution of clinical development programs.

This role could support candidates based in either London or Paris, with an office presence of 60% required.

Key Responsibilities:

• Lead the scientific design, strategy, and oversight of clinical trials in neuroscience or related therapeutic areas.
• Collaborate with cross-functional teams, including clinical operations, regulatory, medical affairs, and biometrics, to ensure clinical programs are executed efficiently and in compliance with regulatory standards.
• Provide medical and scientific expertise to support protocol development, study design, and data interpretation.
• Serve as a key liaison with external stakeholders, including investigators, key opinion leaders, and academic partners.
• Contribute to regulatory submissions, clinical study reports, and publications, ensuring scientific rigor and accuracy.
• Mentor and support junior clinical team members, fostering a culture of collaboration and scientific excellence.

Required Qualifications:

• PhD in a relevant scientific discipline
• Approximately 5 years of industry experience in clinical development, preferably in neuroscience, but not required
• Strong understanding of clinical trial design, regulatory requirements, and Good Clinical Practice (GCP).
• Excellent communication, collaboration, and leadership skills.
• Demonstrated ability to analyze complex clinical data and translate findings into actionable insights.

If you feel like this role could be suited to you, please reach out via DM or email - -talent.com

• Lead the scientific strategy and design of clinical development programs for assigned therapeutic areas or drug candidates.
• Develop clinical trial protocols, amendments, investigator brochures, and other essential study documents, ensuring scientific accuracy and regulatory compliance.
• Provide scientific expertise and oversight throughout the lifecycle of clinical trials, from initiation to database lock and study report writing.
• Interpret clinical trial data, ensuring robust analysis and accurate reporting of results.
• Collaborate with biostatistics and data management teams to define data analysis plans and review study outputs.
• Serve as a key scientific liaison with regulatory authorities (e.g., MHRA, EMA, FDA) for submissions and inquiries.
• Engage with key opinion leaders (KOLs) and investigators to gather insights, foster collaboration, and ensure optimal trial conduct.
• Stay abreast of the latest scientific advancements, competitive landscape, and regulatory guidelines within the relevant therapeutic areas.
• Mentor and guide junior scientists and contribute to the scientific development of the clinical research department.
• Contribute to the preparation of scientific publications and presentations.
• Participate in the evaluation of new drug targets and development opportunities.

• Advanced scientific degree (Ph.D. or M.D.) in a relevant life science discipline (e.g., Pharmacology, Biology, Medicine).
• Minimum of 7-10 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry.
• Demonstrated expertise in clinical trial design (Phase I-IV), execution, and data interpretation.
• Thorough understanding of ICH-Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Proven ability to lead complex projects and cross-functional teams.
• Excellent scientific writing and oral communication skills, with experience presenting complex data.
• Strong analytical and problem-solving capabilities.
• Experience in specific therapeutic areas such as oncology, immunology, or neurology is highly desirable.
• Ability to work effectively in a hybrid environment, balancing remote and in-office responsibilities in London, England, UK .

• Design and execute complex in-vitro and in-vivo preclinical studies to evaluate novel oncology drug candidates.
• Analyze and interpret experimental data, developing robust conclusions and strategic recommendations for project progression.
• Prepare high-quality scientific reports, manuscripts for publication, and presentations for internal and external stakeholders.
• Contribute to the development of regulatory submission documents (e.g., IND, NDA).
• Collaborate effectively with cross-functional teams, including discovery biology, translational medicine, and clinical development.
• Mentor junior scientists and contribute to a positive and innovative research environment.
• Stay abreast of the latest advancements in oncology research, therapeutic modalities, and drug development technologies.
• Ensure all research activities comply with relevant ethical guidelines and regulatory standards.
• Manage external collaborations with academic institutions and contract research organizations (CROs).
• Contribute to the strategic direction of the oncology pipeline.

• Ph.D. in Oncology, Molecular Biology, Pharmacology, or a related life science discipline.
• Minimum of 5 years of post-doctoral or industry experience in cancer research, with a strong track record of scientific achievement.
• Proven expertise in preclinical oncology drug discovery and development, including a deep understanding of cancer biology, immunology, and targeted therapies.
• Proficiency in a range of laboratory techniques relevant to oncology research (e.g., cell culture, molecular biology assays, flow cytometry, western blotting, IHC, animal models).
• Excellent data analysis and interpretation skills, with experience using relevant statistical software.
• Strong written and verbal communication skills, with the ability to present complex scientific information clearly and concisely.
• Demonstrated ability to work independently and as part of a collaborative team in a remote setting.
• Experience in project management and leading research initiatives is highly desirable.
• Familiarity with regulatory requirements for drug development.

• Contribute to the design and development of innovative clinical trial protocols for oncology indications, ensuring scientific rigor and compliance with regulatory requirements.
• Oversee the execution of clinical studies, from site selection and initiation through to study close-out.
• Analyse and interpret complex clinical data, including safety, efficacy, and biomarker data.
• Prepare and present study results for internal stakeholders, regulatory submissions, and scientific publications.
• Collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, R&D, and external investigators.
• Provide scientific and clinical expertise to guide the progression of drug candidates through the development pipeline.
• Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, and other relevant regulations.
• Contribute to the development of scientific strategy and research plans for the oncology portfolio.
• Mentor and guide junior research scientists and clinical trial staff.
• Review and critically evaluate scientific literature relevant to oncology drug development.
• Participate in scientific conferences and represent the company's research efforts.
• Manage relationships with key opinion leaders (KOLs) and external research partners.

• PhD or MD in a relevant scientific discipline (e.g., Oncology, Immunology, Molecular Biology, Pharmacology).
• Minimum of 6 years of experience in clinical research, with a significant focus on oncology drug development.
• In-depth knowledge of oncology therapeutic areas, disease mechanisms, and current treatment landscapes.
• Proven experience in clinical trial design, execution, and data analysis.
• Strong understanding of GCP, regulatory requirements, and drug development processes.
• Excellent scientific writing and communication skills, with a track record of publications.
• Demonstrated ability to work collaboratively in a multidisciplinary, hybrid team environment.
• Strong analytical and problem-solving skills.
• Proficiency in data analysis software and statistical methods.
• Ability to manage multiple projects and deadlines effectively.