Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Locations: Remote from UK/Wales/France only Position Summary: The Clinical Compliance Manager is responsible for the assessment, management, and reporting of serious breaches of GCP and protocol in clinical trials. This role ensures timely escalation, root cause analysis, regulatory communication, and CAPA tracking in alignment with global regulatory requirements (e.g., EMA, MHRA, FDA). The ideal candidate will serve as a subject matter authority on potential serious breach handling and support other activities related to QA across the clinical development portfolio. Key Responsibilities: Lead the assessment and classification of serious breaches in collaboration with QA, Clinical Operations, and Regulatory Affairs. Serve as the primary point of contact for serious breach investigations. Prepare and submit serious breach notifications to applicable regulatory authorities within required timelines. Develop and maintain standard operating procedures (SOPs) related to breach management. Ensure timely and thorough root cause analysis and CAPA development, working closely with functional area leads. Maintain breach documentation and logs in compliance with GCP and inspection expectations. Support audits and regulatory inspections as a subject matter expert (SME) for serious breach. Deliver training and guidance to study teams and sites on breach awareness and reporting procedures. Trend and report breach data to identify process improvements or systemic quality issues. Qualifications: Bachelor’s degree in life sciences, nursing, pharmacy, or related field. 5 years of clinical research experience, with at least 2 years in Clinical Quality, GCP Compliance, or related role. Strong working knowledge of ICH E6(R2/R3), EMA/MHRA/FDA serious breach expectations. Proven experience in CAPA, root cause analysis, and deviation management. Demonstrated ability to communicate complex compliance issues clearly and effectively. Comfortable working in a matrix organization and managing cross-functional customers. Prior experience with clinical quality systems (e.g., Veeva Vault, TrackWise, etc.) is a plus. Knowledge, Skills and Abilities: Thorough knowledge of applicable GxP and appropriate regional regulations Extensive knowledge of the clinical trial process and serious breach reporting Excellent oral and written communication skills (including appropriate use of medical and scientific terminology) Training/mentoring experience Strong attention to detail Effectively works independently or in a team environment Highly developed problem solving skills, risk assessment and impact analysis abilities Strong leadership skills Strong organizational and time management skills including ability to multitask and prioritize competing demands/work load Strong digital literacy; ability to learn and become proficient with appropriate software Proven flexibility and adaptability Ability to qualify for and maintain a corporate credit card with sufficient credit line for business travel Veeva QMS experience a plus