Clinical Research Associate

p Senior CRA or Lead CRA - England, Fully Home Based. /p p br /p p Are you an accomplished Clinical Research Associate seeking a stimulating and pivotal career move? Do you excel in a culture where quality site engagement is prioritised over rigid metrics and where your well-being is a core value? This is the chance to join a clinical research organisation with a strong UK presence. /p p We are specifically looking for candidates based within the South West, London, the Midlands, or the North West regions. /p p br /p p The client, a distinguished global Contract Research Organisation, is looking to recruit a high-calibre CRA II, Senior or Lead CRAs to help drive forward clinical trials in high-impact therapeutic areas. This includes areas such as Oncology, Haematology-Oncology, Rare and Orphan Diseases, and other cutting-edge specialities. You will be instrumental in ensuring the compliant and efficient operation of these studies across a network of key clinical sites. /p p br /p p Why Consider This Opportunity? /p p br /p p The organisation differentiates itself by placing its focus firmly on its people and the quality of their work: /p ul li Empowerment and Quality-First Monitoring: They advocate for a robust and thoughtful approach to site management. Trust is placed in their CRAs, empowering them to manage their sites effectively. They believe that proactive collaboration and sound judgement are more valuable than mandating a minimum number of site visits, offering greater flexibility. /li li Structured Career Advancement: The CRO is deeply committed to nurturing the talents within its team. You can expect clearly defined progression pathways, backed by continual training, mentorship, and development resources to help you achieve your long-term career goals. /li li Meaningful Contribution: Your valuable expertise and insights will actively help refine clinical processes and shape the organisational culture. This commitment to employee engagement is viewed as an essential driver for both their long-term success and the career longevity of their team members. /li /ul p br /p p Your Role as a CRA II / Senior/ Lead CRA /p p br /p p In this home-based and regionally focused role, your primary responsibilities will encompass: /p ul li Managing and overseeing all aspects of the clinical monitoring process for assigned sites, from initial set-up through to final site closure. /li li Cultivating and maintaining strong, professional rapport with research investigators and site personnel. /li li Strictly ensuring all trial activities adhere to the approved protocol, Good Clinical Practice (GCP), and all relevant UK/European regulatory frameworks. /li li Contributing effectively to the preparation and review of essential study-related documentation. /li li Providing guidance and support to less experienced CRAs, particularly at the Lead CRA level. /li /ul p br /p p Essential Candidate Profile /p p br /p p To thrive in this position, you will need: /p ul li Substantial, independent clinical monitoring experience gained within a clinical trial setting. /li li A comprehensive and up-to-date knowledge of GCP and UK regulatory requirements. /li li Outstanding interpersonal, organisational, and analytical problem-solving capabilities. /li li A naturally proactive, diligent, and detail-oriented work ethic. /li li Prior experience in one or more of the focus therapeutic areas (e.g., Oncology, Haematology-Oncology, Rare Diseases) would be a considerable advantage. /li /ul p br /p p If you are seeking a truly rewarding career environment where your expertise is genuinely respected, your professional development is actively supported, and you can play a direct part in bringing innovative medicines to patients across the UK, we strongly encourage your application. /p p To Express Your Interest: Please forward your cv to r.kelly@completeclinicalsolutions.com /p