Clinical Project Manager

• Lead clinical study start-up activities, translating study requirements and response assessment criteria into project plans, timelines, milestones, communication plans and study documentation.
• Manage project execution and stakeholder communications, providing timely updates to sponsor representatives, project teams, sites, Business Development and leadership.
• Monitor critical project success factors, resource requirements, risks, data collection activities and overall delivery against agreed project expectations.
• Own key financial activities, including monthly billing, forecasting, scope reviews, amendments, pass-through costs and the project information required to support revenue reporting.
• Maintain strong knowledge of project contracts, study protocols and Standard Operating Procedures (SOPs), partnering with Quality Assurance to address deviations and communicate protocol updates.
• Lead, train and support cross-functional project teams, establishing clear project expectations and partnering with functional leaders on coaching and development.
• Support Business Development activities through capabilities discussions, sponsor meetings and polished Investigator Meeting presentations.
• Coordinate study closeout and applicable submission activities, ensuring project deliverables are completed appropriately.
• Where applicable, provide people-management support, including setting expectations, coaching, performance management, hiring and onboarding.

What We Look For

• Bachelor’s degree or equivalent practical experience; education in life sciences, pharmacy, nursing or another healthcare field is highly desirable.
• 1–3 years of clinical trials experience within a contract research organization (CRO) or pharmaceutical research environment, preferably in project management.
• Previous project or management experience supporting the clinical development of investigational medicines.
• Working knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines and relevant clinical research regulations.
• Medical imaging experience is preferred.
• Experience with common project and business productivity tools, including Microsoft Word and Excel; Microsoft Project experience is preferred.
• Demonstrated ability to organize and lead complex clinical projects while managing timelines, financial activities and multiple stakeholders.
• Strong written and verbal communication skills with a collaborative, professional approach.
• Ability to work effectively with sponsors, investigative sites and cross-functional teams in a quality-focused clinical research environment.
• At Clario, a part of Thermo Fisher Scientific, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence.
• It’s a cause that unites and inspires us.
• It’s why we come to work—and how we empower our people to make a positive impact every day.
• Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.