Clinical Study Co-Ordinator

Join to apply for the Clinical Study Co-Ordinator role at Charles River Laboratories . For 75 years, Charles River employees have worked together to assist in the discovery, development, and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales, or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. Job Summary To support the continued growth of our clinical bioanalytical team, we are seeking a Clinical Study Coordinator within the Department of Immunology, Bioanalysis & Biomarkers located at our site at Clearwater House in Riccarton, Edinburgh. This is a 12-month fixed-term contract opportunity. The successful candidate will act as a key link between our Sample Management team and other stakeholders, requiring excellent communication, problem-solving skills, and adaptability to changing priorities. A detail-oriented and proactive individual who thrives in a fast-paced, dynamic environment. This role involves both laboratory and office-based responsibilities, requiring strong collaboration skills and a flexible approach to teamwork. Key Responsibilities Include Clinical sample coordination, including liaising with stakeholders, interpreting protocols, drafting documents, creating and managing clinical manifests, reconciliation, and importing data into Watson LIMS. Sample receipt, management, shipping, and delivery. Maintaining accurate records of samples and documentation. Tube and sample preparation, laboratory organization, and cleaning duties. Maintenance of storage equipment. Additional Responsibilities and Development Opportunities Line management of junior staff. Acting as deputy for the supervisor. Preparation of reagents and solutions. Using laboratory equipment such as balances and centrifuges. Monitoring and maintaining consumables and equipment records. Minimum Requirements BSc or MSc degree. Relevant experience is a plus. Ability to work independently and manage workload. Strong data interpretation, problem-solving, organizational, and communication skills. Proficiency in Microsoft Excel, including formulas. The salary starts at £27,163.48 per annum, subject to experience. Initial training will be at Elphinstone, Tranent, followed by work at Clearwater House, Riccarton. About Safety Assessment Charles River provides safety assessment services to expedite preclinical drug development, with state-of-the-art facilities and expert guidance, conducting around 300 IND programs annually. About Charles River We are a global early-stage contract research organization with over 20,000 employees across 110 facilities in more than 20 countries, supporting clients from target discovery through preclinical development and clinical testing. We are committed to diversity and inclusion, aiming to reflect the talents of all individuals. #J-18808-Ljbffr