Serve as the primary escalation point for assigned clinical trials, projects, and programs, ensuring timely resolution of imaging-related issues.
Monitor imaging activities at clinical trial sites and approved imaging centers to ensure timely and high-quality deliverables.
Leverage tools, data, and cross-functional resources to support informed decision-making and foster collaboration with global clinical trial teams and sites.
Partner with internal teams and external partners to ensure consistent, high-quality engagement across study teams and global sites.
Coordinate and track local, regional, and global imaging deliverables, including issue identification, contingency planning, and resolution.
Develop and implement risk mitigation plans to support enrollment targets and database lock timelines.
Partner with internal and external stakeholders to remove operational barriers and enable successful trial execution at site and country levels.
Apply project management and clinical trial expertise to align imaging deliverables with scope, timelines, and budget.
Lead onboarding and oversight of Third-Party Organizations (TPOs), ensuring adherence to performance metrics and budget compliance.
Coordinate operational aspects of imaging trials, including protocol development, imaging plan execution, staff training, and documentation.
Manage relationships with imaging centers, triage technical support for image acquisition, reconstruction, troubleshooting, and data transfer.
Collaborate cross-functionally to maintain project timelines from planning through completion, with a focus on imaging data collection and analysis.
Proactively identify and escalate risks and barriers, coordinating mitigation strategies to maintain project momentum.
Continuously evaluate team activities and processes to propose alternate solutions and process improvements.
Perform other duties as assigned.
Requirements
Bachelor’s degree or equivalent experience (scientific or health-related field preferred)
2+ years clinical research experience or relevant clinical experience in a scientific or health-related field
Understanding of Good Clinical Practice principles
Clinical research experience, preferably in pharmaceutical development or a clinical research organization
Experience in nuclear medicine or radiopharmaceuticals
Applied knowledge of trial execution methodology, processes, and tools
Demonstrated strong teamwork and collaboration skills and the ability to work cross-culturally with global colleagues and Third-Party Organizations
Effective and influential communication, self-management, and organizational skills
Demonstrated ability to manage complex situations through problem-solving, critical thinking and navigating ambiguity
Flexibility to adjust to altered priorities
Proficient with Microsoft Outlook, Word, Excel, Teams, Planner, and PowerPoint.
Benefits
Eligible for a company bonus (depending on company and individual performance)
Comprehensive benefit program including medical, dental, vision and prescription drug benefits
Eligibility to participate in a company-sponsored 401(k) and pension
Vacation benefits
Flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
Life insurance and death benefits
Certain time off and leave of absence benefits
Well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical researchproject managementrisk mitigationprotocol developmentimaging data collectiondata analysistrial execution methodologyproblem-solvingcritical thinkingnuclear medicine
Soft skills
teamworkcollaborationcommunicationself-managementorganizational skillsflexibilityability to navigate ambiguityinfluential communicationcross-cultural collaborationprocess improvement
Certifications
Bachelor’s degreeGood Clinical Practice certification