Clinical Research Associate

Ready to take ownership of early-phase clinical trials while gaining the variety, autonomy and visibility that larger CROs often can't offer?Join a boutique, early-phase CRO partnering with innovative biotechnology companies across a varied portfolio of clinical trials, including psychedelic medicine, respiratory disease, oncology and other therapeutic areas.With a close-knit team of approximately 30-40 people, the company offers a collaborative, supportive culture where individuals can make a visible contribution. Unlike larger CRO environments, the role provides exposure to different responsibilities and opportunities to develop in areas that match your interests, including clinical project management.The opportunityWe are looking for a Clinical Research Associate who can independently manage monitoring activities and contribute effectively from an early stage. You will work primarily on Phase I and Phase II studies, supporting small biotech sponsors across a range of therapeutic areas. Alongside site monitoring, the position will include elements of eTMF management and broader clinical trial responsibilities.This could be an excellent opportunity for an experienced CRA seeking greater variety, autonomy and progression within a smaller organisation. Candidates with relevant academic research experience are also encouraged to apply, provided they have the practical monitoring experience required to work independently.Responsibilities:Conduct site initiation, routine monitoring and close-out visitsPerform source data verification and ensure study data are accurate and completeMaintain effective relationships with investigational sites and study teamsSupport eTMF maintenance and managementEnsure studies are conducted in accordance with protocols, SOPs, GCP and applicable regulationsIdentify and help resolve site-level issuesContribute to broader clinical trial activities as requiredCollaborate closely with colleagues during regular office and training daysKey Skills and Requirements:Essential:At least two years of CRA or relevant independent clinical monitoring experienceThe ability to manage monitoring activities without close supervisionExperience conducting site visits and source data verificationA good understanding of GCP and clinical trial processesBased in London or within practical travelling distance of London-based study sitesAn enthusiastic, adaptable and collaborative approachComfortable working in a small, hands-on environment where priorities can changeDesirable:Early-phase clinical trial experience, particularly Phase I or Phase IIExperience presenting or conducting site initiation visitsExperience taking studies through to close-outeTMF management experienceClinical Trial Coordinator experienceExposure to oncology, respiratory, psychedelic medicine or other specialist therapeutic areasWorking pattern and travelThe role is hybrid, with in-person collaboration at the office on the first and third Tuesday of each month. Quarterly training sessions are also held in person and may coincide with an office day.Monitoring sites are primarily located in London. Travel varies according to study activity, averaging approximately five visits per month and rarely exceeding two visits per week.If you are having difficulty in applying or if you have any questions, please contact Elis Jones at Now:If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page. Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical 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 -