428 Medical Researchers jobs in the United Kingdom

• Lead the scientific design and development of clinical trial protocols for oncology studies.
• Contribute to the preparation and submission of regulatory documents (e.g., IND, NDA).
• Oversee data collection, cleaning, and analysis, ensuring accuracy and completeness.
• Monitor trial progress and identify potential risks and challenges, implementing mitigation strategies.
• Collaborate with principal investigators and study site staff to ensure protocol adherence.
• Prepare scientific reports, publications, and presentations.
• Stay abreast of the latest advancements in oncology research and clinical trial methodologies.
• Mentor junior members of the research team.
• Ensure all research activities are conducted in compliance with GCP, ICH guidelines, and other applicable regulations.

• PhD or equivalent in a relevant scientific field (e.g., Pharmacology, Biology, Oncology).
• Minimum of 5-7 years of experience in clinical research within the pharmaceutical industry, with a focus on oncology.
• Demonstrable experience in designing and managing Phase I-III clinical trials.
• Strong understanding of oncology drug development and relevant therapeutic areas.
• Excellent knowledge of regulatory requirements (FDA, EMA) and Good Clinical Practice (GCP).
• Exceptional analytical, problem-solving, and critical thinking skills.
• Proficiency in statistical analysis software and clinical data management systems.
• Superior written and verbal communication skills.
• Ability to work independently and as part of a remote, collaborative team.

• Design and develop clinical trial protocols in alignment with research objectives and regulatory requirements.
• Oversee the execution of clinical trials, ensuring adherence to protocol, GCP, and other relevant guidelines.
• Manage and analyze clinical trial data, interpret results, and prepare comprehensive study reports.
• Collaborate with principal investigators and site staff to ensure high-quality trial conduct.
• Prepare regulatory submission documents, including Investigator's Brochures and IND filings.
• Stay updated on scientific literature, emerging therapeutic areas, and competitive intelligence.
• Provide scientific and technical guidance to clinical study teams.
• Identify and address potential risks and challenges in clinical trial execution.
• Contribute to the development of clinical development strategies for new drug candidates.
• Present study findings at scientific meetings and conferences.
• Ensure the safety and well-being of trial participants throughout the study.

• PhD or MSc in a relevant life science discipline (e.g., Pharmacology, Biochemistry, Medicine, Biology).
• Minimum of 5-8 years of experience in clinical research within the pharmaceutical or biotechnology industry.
• Demonstrated experience in designing and managing Phase I, II, or III clinical trials.
• In-depth knowledge of drug development processes, regulatory affairs, and ICH-GCP guidelines.
• Strong understanding of statistical principles and clinical data analysis methods.
• Excellent scientific writing and presentation skills.
• Proven ability to work effectively in a cross-functional team environment.
• Strong project management and organizational skills.
• Excellent problem-solving and critical thinking abilities.
• Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is desirable.

• Lead the scientific design and development of Phase I-IV clinical trial protocols in oncology, ensuring alignment with regulatory requirements and research objectives.
• Oversee the execution of clinical studies, providing scientific and operational guidance to study teams, investigators, and site personnel.
• Analyze and interpret clinical trial data, contributing to the development of study reports, regulatory submissions, and publications.
• Collaborate closely with cross-functional teams, including data management, biostatistics, regulatory affairs, and medical affairs.
• Develop study-specific clinical guidelines, case report forms (CRFs), and other essential study documents.
• Ensure compliance with Good Clinical Practice (GCP), FDA, EMA, and other relevant regulatory guidelines.
• Evaluate and select appropriate clinical endpoints and biomarkers for oncology studies.
• Stay abreast of the latest scientific advancements, clinical trial methodologies, and therapeutic landscape in oncology.
• Contribute to the strategic planning of the clinical development pipeline.

Job Title: Clinical Research Coordinator (Band 6 Nurse)

Contract Type: Part-Time (2–3 days/week)

Overview:

We are seeking a skilled and motivated Band 6 Nurse to support clinical research activities as a Clinical Research Coordinator. This part-time role offers an excellent opportunity to contribute to impactful research while maintaining a flexible schedule.

Key Responsibilities:

• Identify and recruit eligible patients for clinical trials.
• Perform accurate and timely data entry into study databases.
• Collaborate with research and clinical teams to ensure protocol compliance.
• Maintain high standards of documentation and regulatory adherence.

Requirements:

• Registered Band 6 Nurse with relevant clinical experience.
• Demonstrated experience in patient identification and data entry.
• Strong attention to detail and organizational skills.
• Must be available to work every Wednesday, plus two additional weekdays.

Please submit your CV or get in touch via email:

Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.

As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.

You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.

This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.

Key Responsibilities

• Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
• Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
• Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
• Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.

Requirements

• A medical degree (MD) - essential
• Full and current GMC registration - essential.
• Strong background in clinical research / clinical trials.
• Proven experience as a Clinical Research Physician.
• Strong knowledge of regulatory guidelines.
• Excellent organisational, communication and analytical skills.

Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.

Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.

As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.

You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.

This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.

Key Responsibilities

• Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
• Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
• Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
• Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.

Requirements

• A medical degree (MD) - essential
• Full and current GMC registration - essential.
• Strong background in clinical research / clinical trials.
• Proven experience as a Clinical Research Physician.
• Strong knowledge of regulatory guidelines.
• Excellent organisational, communication and analytical skills.

Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.