Clinical Trial Associate (CTA)

Northreach is a dynamic recruitment agency that connects businesses with top talent in the Advanced Therapies sector. Our mission is to provide a seamless and personalised recruitment experience for clients and candidates, and to create a positive work environment that encourages equality, innovation, and professional growth. About Us: My client is an innovative biotechnology company based in London, dedicated to advancing cell and gene therapies to address unmet medical needs. As a growing organisation at the forefront of Advanced Therapy Medicinal Products (ATMPs), my client is seeking a highly motivated Clinical Trial Associate (CTA) to support our clinical operations team in delivering high-quality trials that drive innovation in patient care. For the right person, contractors can also be considered. Role Overview: The Clinical Trial Associate (CTA) will play a key role in supporting the planning, execution, and management of our clinical trials. You will work closely with Clinical Project Managers (CPMs) and other cross-functional teams to ensure compliance with regulatory requirements and smooth trial operations. This is an excellent opportunity for an organised and detail-oriented professional who wants to contribute to groundbreaking advancements in cell and gene therapy. Key Responsibilities: Assist in the coordination and administration of clinical trials from start-up to close-out. Maintain and manage Trial Master File (TMF) documentation to ensure compliance with regulatory standards. Support the preparation, submission, and tracking of essential documents, ethics submissions, and regulatory approvals. Coordinate communication with internal teams, external vendors, CROs, and clinical sites. Track and manage study-specific timelines, budgets, and milestones. Assist in organising investigator meetings, site training, and other trial-related activities. Ensure adherence to ICH-GCP guidelines and company SOPs. Manage clinical supplies and documentation related to investigational products. Provide administrative support for contracts, invoices, and site payments. Requirements: Bachelor’s degree in Life Sciences, Pharmacy, or a related field. Previous experience in a CTA role within a biotech, pharmaceutical, or CRO environment. Strong understanding of ICH-GCP guidelines and clinical trial processes. Familiarity with TMF management and regulatory document submission. Excellent organisational skills with a high level of attention to detail. Strong communication and interpersonal skills. Ability to work in a fast-paced, collaborative environment. Proficiency in Microsoft Office (Word, Excel, PowerPoint) and clinical trial management systems (CTMS) is advantageous. Why Join Us? Be part of a cutting-edge biotech driving advancements in advanced therapies. Work in a dynamic and collaborative environment with industry-leading experts. Competitive salary and benefits package. Career development opportunities in a rapidly growing company. Northreach is an equal opportunity employer and we do not discriminate against any employee or applicant for employment based on race, colour, religion, sex, national origin, disability, or age. We are committed to promoting diversity, equity, and inclusion in the workplace and hiring practices, therefore only partner with businesses that promote DEI. We strive to create a welcoming and inclusive environment for all employees. Seniority Level Associate Employment Type Full-time Job Function Research Industries Biotechnology Research and Pharmaceutical Manufacturing #J-18808-Ljbffr