Associate / Bachelor's degree1+ year clinical trials / researchGCP / ICH / FDA complianceMicrosoft Office SuiteProject documentation & reportingClinical trial operationsStakeholder communicationProject finance supportMedical imaging experienceCross-functional collaborationProblem-solving & prioritization
Job Description
Assistant Clinical Project Manager position at Clario (part of Thermo Fisher Scientific) supporting medical imaging clinical trials. The role involves coordinating project activities, managing documentation, communicating with sponsors and sites, and partnering with cross-functional teams to ensure successful study delivery. Requires an associate degree minimum (bachelor's preferred) and at least 1 year of experience in pharmaceutical development, clinical trials, or related fields.
Overview
Join Clario, a part of Thermo Fisher Scientific, and help advance medical imaging clinical trials that support the development of life-changing therapies around the world. As an Assistant Clinical Project Manager within the Medical Imaging business, you will play a key role in supporting the successful delivery of clinical studies by coordinating project activities, managing documentation, communicating with sponsors and sites, and partnering with cross-functional teams to ensure study milestones are achieved.
What We Offer
•Competitive pay and incentives
•Provident fund and medical insurance
•Engaging employee programs and local events
•Modern office spaces and remote work flexibility
•Opportunities for professional growth and career development within a global organization
Responsibilities
•Support Clinical Project Managers in the planning, startup, execution, monitoring, and closeout phases of medical imaging studies
•Develop, maintain, and organize project-related documentation, reports, presentations, and study materials
•Review and edit project presentations, status reports, and client-facing communications to ensure accuracy and consistency
•Participate in project meetings, conference calls, training sessions, and cross-functional discussions to support project execution
•Review and interpret study protocols and project requirements to support operational readiness and study compliance
•Serve as a liaison between project teams and cross-functional departments to facilitate timely completion of study deliverables
•Monitor project activities and communicate study needs, risks, issues, and progress updates to project leadership
•Support project finance activities, including documentation updates resulting from scope changes, invoice reconciliation follow-up, and forecasting reports
•Monitor internal workflows and data flow processes to ensure project tasks are completed within agreed timelines
•Respond to client and stakeholder inquiries in a professional, timely, and customer-focused manner
•Communicate project status updates to clients, sponsors, sites, and internal stakeholders
•Verify protocol-specific imaging requirements and ensure discrepancies or queries are appropriately identified and escalated
•Support issue tracking, client concern resolution, and follow-up activities to ensure timely project execution
•Coordinate the distribution, management, and tracking of site-facing materials and study-related logistics
•Serve as acting Project Manager in the absence of the assigned Clinical Project Manager when required
•Contribute to process improvement initiatives and provide recommendations that enhance operational efficiency and study delivery
•Ensure compliance with Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, FDA regulations, company procedures, and study-specific requirements
What We Look For
•Associate degree required; Bachelor's degree preferred in Life Sciences, Healthcare, Clinical Research, Business Administration, or a related field
•Minimum 1 year of experience in pharmaceutical development, clinical trials, clinical research, healthcare, medical imaging, or a related industry
•Understanding of clinical research processes, drug development, and clinical trial operations preferred
•Strong proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, Outlook, and Teams
•Excellent organizational, time management, prioritization, and multitasking skills
•Strong interpersonal, verbal, and written communication skills with the ability to communicate effectively in English
•Detail-oriented with strong documentation, follow-up, and quality review capabilities
•Ability to work independently while collaborating effectively within cross-functional and global teams
•Strong problem-solving skills with the ability to manage competing priorities and changing business needs
•Proactive, customer-focused, and results-oriented approach to project support and delivery
•Experience supporting medical imaging, healthcare, or clinical technology programs is preferred
•Ability to maintain professionalism, adaptability, and a positive attitude in a fast-paced environment
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