Associate – Clinical Trial Imaging Operations
Location
United States
Posted
9 days ago
Salary
$65.3K - $161.7K / year
Bachelor Degree2 yrs expEnglish
Job Description
• 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.
Job 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
- medical, dental, vision, and prescription drug 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)
- eligibility to participate in a company-sponsored 401(k)
- pension
- vacation benefits
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