Responsable Opérationnel / Manager F/H
Thermo Fisher Scientific
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join us as a Manager, Clinical Operations - And take on a leadership role in overseeing clinic operations, driving process improvements, managing a team of healthcare professionals, ensuring compliance with regulatory standards, and enhancing patient care and service quality. 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. Team Leadership & Development • Lead, support, and develop a team of Clinical Operations professionals. • Manage the full employee lifecycle, including interviews, recruitment and staff selection, onboarding, goal setting, performance management, coaching, and Manage and conduct induction/orientation programs for all new employees, Conduct structured performance and skills assessments (e.g., MAST – remote or on-site, RAP, PAFR) to ensure high-quality study execution and continuous Identify development needs, address performance concerns constructively, administrative matters in line with company policies. • Ensure employee documentation (CVs, training records, position and Study Delivery & Resource Management
- Drive the successful delivery of clinical trials conducted at the country level.
- deliverables, quality expectations, and business goals.
- Support staff allocation in line with local resourcing processes and study
- Promote and support the implementation of risk-based monitoring principles.
- Identify quality concerns, request Quality Assurance (QA) audits when
- Excellent people management, mentoring, and supervisory skills.
- Strong expertise in clinical trial operations and monitoring.
- Strong knowledge of risk-based monitoring and quality management principles.
- Comprehensive knowledge of applicable of ICH/GCP, company SOPs/WPDs, FDA guidelines and relevant regulatory requirements
- Solid knowledge of therapeutic areas and medical terminology.
- Ability to critically evaluate medical and clinical research data.
- Proven ability to anticipate risks, solve complex problems, and escalate appropriately.
- Continuous improvement mindset with the ability to drive operational excellence and process optimization.
- Quality-focused with sound negotiation and decision-making skills.
- Proficiency in clinical systems and performance management tools.
- Advanced computer skills including data entry, documentation management, and information retrieval.
- Excellent command of English (written and spoken).
- Willingness and ability to travel as required.
$95k - $105k
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