Associate - Clinical Trial Imaging Operations
Location
United States
Posted
9 days ago
Salary
$65.3K - $161K / year
No structured requirement data.
Job Description
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
Associate, Senior Associate, Manager – Clinical Trial Imaging Operations
Primary Responsibilities:
This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position can change over time and can include additional responsibilities not specifically described in the 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
Minimum Qualification 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
Additional Skills/Preferences:
- 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.
- Consistent, successful demonstration of project management behaviors with excellent oral and written communication skills; able to communicate clearly and succinctly with team members; reflects and committed to Team Lilly’s values.
- Overnight travel may be required and is estimated at 10%
- Position location: Remote or Philadelphia
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is
$65,250 - $161,700Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for 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; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
Related Guides
Related Categories
Related Job Pages
More Clinical Operations Jobs
Manager, Clinical Operations - Organ Transplant
VituityAt Vituity you are part of a larger team that is driven by our purpose to improve lives. We are dedicated to transforming healthcare through our culture by working together to tackle healthcare’s most pressing challenges from the inside. Even when you are working remotely, you are an important part of the Vituity Community. We offer plenty of opportunities to engage with other Vitans through a variety of virtual meet-and-greets, events and seminars. Monthly wellness events and programs such as yoga, HIIT classes, and more. Trainings to help support and advance your professional growth. Team building activities such as virtual scavenger hunts and holiday celebrations. Flexible work hours. Opportunities to attend Vituity community events including LGBTQ+ History, Día de los Muertos Celebration, Money Management/Money Relationship, and more.
Remote, Nationwide – Seeking Manager, Clinical Operations - Organ Transplant Everybody Has A Role To Play In Transforming Healthcare At Vituity you are part of a larger team that is driven by our purpose to improve lives. We are dedicated to transforming healthcare through our cu...
Clinical Project Manager leading clinical research and managing cross-functional teams
This leadership role involves co-leading a team of experienced Sexual Assault Nurse Examiners (SANEs) in delivering live quality assurance, mentorship, and peer review during forensic examinations via telehealth. The coordinator will support all facets of clinical operations, including program implementation, teleSANE team management, clinical training development, and partner site success.
The Clinical Project Manager II will manage the delivery of clinical study requirements according to the protocol, regulations like GCP and ISO 14155, site needs, and project timelines, while balancing resource constraints. Responsibilities also include implementing risk-based monitoring, overseeing data review for compliance, and training junior staff.