151 Scientific Research jobs in London

• Conduct site initiation visits to assess the feasibility of recruitment and ensure regulatory compliance.
• Perform routine monitoring visits (on-site and remote) to review source data, investigational product accountability, and regulatory documentation.
• Identify, evaluate, and resolve site-level issues and risks, escalating where necessary.
• Build and maintain strong relationships with investigators, study coordinators, and site staff.
• Ensure timely and accurate submission of all required study-related documentation.
• Train and mentor junior CRAs, providing guidance and support.
• Contribute to the development and review of study protocols and other essential documents.
• Participate in the preparation of site audit readiness and respond to audit findings.

• Bachelor's degree in life sciences, nursing, or a related field; advanced degree preferred.
• Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
• Thorough understanding of ICH-GCP guidelines and relevant regulatory requirements.
• Proven experience in monitoring multiple clinical trials simultaneously.
• Excellent communication, interpersonal, and problem-solving skills.
• Ability to work independently and manage time effectively.
• Proficiency in electronic data capture (EDC) systems and other clinical trial management software.
• Willingness to travel up to 50% of the time within the assigned territory.

• Conduct site initiation, interim monitoring, and close-out visits in accordance with clinical trial protocols and GCP guidelines.
• Verify the accuracy, completeness, and integrity of clinical trial data by reviewing source documents and case report forms (CRFs).
• Ensure compliance with all regulatory requirements, including local regulations and ICH-GCP.
• Identify, document, and resolve site-related issues and discrepancies in a timely manner.
• Train and support site staff on study procedures, protocol requirements, and data collection.
• Build and maintain strong working relationships with investigators, site staff, and study sponsors.
• Prepare monitoring reports and track action items to ensure timely resolution.
• Assist in the selection and qualification of new investigational sites.
• Contribute to the development and review of study-related documents, such as protocols and informed consent forms.
• Manage investigational product accountability and ensure adherence to drug storage and dispensing procedures.

• Bachelor's degree in a life science, nursing, or related discipline.
• Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
• Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Proven experience in monitoring clinical trial sites and managing data integrity.
• Excellent written and verbal communication skills.
• Strong organisational and time management abilities, with the capacity to manage multiple priorities.
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel to investigational sites as required (up to 50%).
• Experience in specific therapeutic areas, particularly related to community health or social care, is a plus.

• Lead and manage a team of CRAs, providing training, mentorship, and performance management.
• Oversee the planning, execution, and monitoring of multiple clinical trials in oncology.
• Ensure compliance with study protocols, GCP, FDA, EMA, and other relevant regulatory guidelines.
• Conduct site selection, initiation, monitoring, and close-out visits.
• Build and maintain strong relationships with principal investigators, site staff, and other stakeholders.
• Review and approve site-generated documentation, including source documents, case report forms (CRFs), and regulatory binders.
• Identify and resolve site-level issues and deviations promptly.
• Contribute to the development of clinical trial protocols, Investigator's Brochures, and other essential documents.
• Manage study budgets and timelines, ensuring efficient resource allocation.
• Prepare and present trial progress reports to internal and external stakeholders.
• Stay updated on the latest developments in oncology research and clinical trial methodologies.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. Advanced degree preferred.
• Minimum of 6-8 years of experience as a Clinical Research Associate, with at least 2 years in a lead or supervisory role.
• Extensive experience in oncology clinical trials is mandatory.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
• Proven experience in site management, monitoring, and auditing.
• Excellent leadership, communication, interpersonal, and problem-solving skills.
• Ability to travel extensively (up to 60-70%) as required by the role.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Strong organizational skills and attention to detail.

• Conduct site feasibility and selection visits.
• Initiate, monitor, and close out clinical trial sites according to protocol and regulatory guidelines.
• Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and other applicable regulations.
• Perform Source Data Verification (SDV) and ensure data accuracy and integrity.
• Verify regulatory compliance at study sites, including review of essential documents.
• Train and mentor site staff on study-related procedures and requirements.
• Manage site-specific issues and facilitate resolution of queries.
• Build and maintain strong working relationships with investigators and site personnel.
• Prepare site monitoring reports and track action items.
• Ensure timely submission of all required study documentation.
• Participate in investigator meetings and other project-related meetings.
• Contribute to the development and review of clinical trial protocols and other study documents.

• Proven experience as a Clinical Research Associate (CRA) or equivalent role within the pharmaceutical or biotechnology industry.
• In-depth knowledge of clinical trial processes, GCP, ICH guidelines, and regulatory requirements.
• Experience with site management and monitoring activities.
• Strong understanding of medical terminology and clinical trial documentation.
• Excellent organizational, time management, and problem-solving skills.
• Exceptional interpersonal and communication skills, with the ability to build rapport with site staff.
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel frequently to clinical sites.
• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Previous experience in specific therapeutic areas is a plus.

SRA/ Scientist I – Nanoparticle Formulations

Are you a nanoparticle scientist with a strong background in lipid nanoparticle (LNP) formulation and a passion for drug delivery innovation? Join a growing biotech R&D team in London and help shape the future of advanced therapeutics.

THE COMPANY

This pioneering fast pace biotech is developing next-generation nanoparticle technologies for gene delivery and advanced drug platforms. Based in London, the team works at the forefront of nanotechnology and drug delivery science, applying creativity and collaboration to solve some of the most complex challenges in therapeutic development. The company are at an exciting stage with fast process projected in their pipeline over the next 12 months.

THE ROLE

As SRA/ Scientist I – Nanoparticle Formulations, you will design, synthesise, and characterise nanoparticle systems for drug and gene delivery applications. You’ll work closely with senior scientists and the Founder on high-impact R&D projects, contributing to the development and optimisation of nanoparticle platforms while gaining experience in scaling up manufacturing processes. This is a lab-based position, requiring strong technical skills, problem-solving ability, and a growth mindset. The company are at a very exciting stage where there are considerable growth plans which will offer the opportunity for you to grow rapidly.

ABOUT YOU

You’ll excel in this role if you have:

• A Master’s degree in Chemistry, Nanotechnology, or related field with at least 2 years’ industry experience in nanoparticle R&D, OR a PhD in a relevant discipline.
• Proficiency in the following analytical techniques: DLS, HPLC, TFF .
• Strong background in lipid nanoparticle (LNP) platforms.

Nice to have:

• Purification experience.
• Microfluidics-based nanoparticle synthesis.
• Additional scale-up expertise.

This is a Permanent, Full-time, onsite laboratory role in Greater London.

If this sounds like your next career step, apply now.

I look forward to hearing from you!