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Clario develops technology and services that support clinical trials from study initiation through implementation. Its clinical trial management platform brings together solutions for electronic clinical outcome assessments, cardiac safety, medical imaging, precision motion, and respiratory monitoring across therapeutic areas such as oncology, cardiology, and neurology. Clario also applies artificial intelligence to endpoint analysis, helping research teams collect consistent trial data while supporting patient privacy and safety. The company works with decentralized and hybrid study models and serves clinical research programs across a global network of countries. Careers at Clario offer opportunities to contribute to healthcare technology, clinical data operations, and the development of tools used in drug research.
Senior Lead Clinical Project Manager
Lead global clinical research studies at Clario, part of Thermo Fisher Scientific, overseeing delivery, teams, compliance, risk, and operational performance.
Description
- Oversee global clinical study management and project delivery.
- Assess study progress, resource needs, and team workloads, then implement adjustments and mitigation plans.
- Identify, assess, and reduce risks across assigned studies and programs.
- Handle escalations and resolve operational, client, and project issues.
- Help Clinical Project Managers communicate study status, risks, timelines, and deliverables to clients.
- Coordinate collaboration among internal and external stakeholders across functions.
- Organize and lead regular project status meetings.
- Manage assigned studies from start-up through execution and closeout.
- Guide study teams across therapeutic areas and programs.
- Work with senior leaders to prioritize deliverables, address resource needs, and share critical project updates.
- Improve operations through ongoing process improvement initiatives.
- Lead departmental initiatives from planning through execution, communication, training, and progress reporting.
- Lead therapeutic area or imaging operational readiness and implement new processes and procedures.
- Track operational challenges and recommend ways to improve study delivery, quality, and efficiency.
- Coach, mentor, and develop project management team members.
- Help onboard and train new team members.
- Allocate team assignments and distribute workloads.
- Set and uphold departmental standards, SOP compliance, and study management practices.
- Review and revise project management and therapeutic team procedures.
- Take on other duties, assignments, and special projects as needed.
Requirements
- Bachelor's degree in life sciences, pharmacy, nursing, or a related field; a master's degree is preferred.
- 5–10 years of clinical research experience in a CRO, pharmaceutical, biotechnology, or related clinical development setting, including substantial project management responsibility.
- Prior people management and leadership experience in clinical development, clinical operations, or clinical trial management.
- Strong understanding of clinical trial processes, project management methods, and drug development practices.
- Working knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and FDA regulations.
- Experience supporting global clinical studies and leading cross-functional teams across locations.
- Medical imaging experience is preferred.
- Demonstrated ability to coach, mentor, and develop team members.
- Strong organization, prioritization, problem-solving, and decision-making skills.
- Excellent written and verbal communication, including the ability to communicate effectively in English with internal and external stakeholders.
- Proficiency with Microsoft Office and project management tools.
- Attention to detail and the ability to manage competing priorities and adapt to changing business needs.
- Valid passport and ability to travel up to 20% as needed.
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