Why join us? This is an exciting time to join OneOncology. Our values-driven culture reflects our startup enthusiasm supported by industry leaders in oncology, technology, and finance. We are looking for talented and highly-motivated individuals who demonstrate a natural desire to improve and build new processes that support the meaningful work of community oncologists and the patients they serve.

Job Description:

Role Summary: The Clinical Trial Manager will report to Sr. Manager, Study Operations. This role will play a critical role in supporting oncology clinical research by supporting site and sponsor during the enrollment and maintenance period of a trial. This position requires a strong understanding of oncology clinical trials, patient recruitment strategies, and research site operations within a Site Management Organization (SMO).

Responsibilities:

• Collaborate with research sites to evaluate their ability to meet sponsor and CRO requirements, including patient recruitment, resources, and infrastructure.

• Create and generate site performance metrics to track enrollment trends and site performance to be discussed with sites on a regular basis.

• Support the overall execution of a clinical trial through the network including proactively identifying potential issues and enrollment barriers and developing strategies to address.

• Utilize clinical trial databases, EMRs, and other data sources to assess patient availability and recruitment.

• Work closely with principal investigators, site staff, and study sponsors to align site metrics with trial objectives.

• Support sites with data entry.

• Stay up to date on industry trends, regulatory requirements, and emerging technologies in clinical trial feasibility and analytics.

• Additional responsibilities as assigned to help drive our mission of improving the lives of everyone living with cancer.

Required or Preferred Qualifications:

• Bachelor’s degree in life sciences, healthcare, data analytics, or a related field (Master’s degree preferred).

• 2+ years of experience in clinical trial feasibility, site selection, or data analytics, preferably within oncology research.

Essential Competencies:

• Experience in an SMO or working with research sites.

• Prior experience working with CROs, sponsors, or site networks

• Experience working clinical trial management systems (CTMS).

• Understanding of clinical research regulations (ICH-GCP, FDA, etc.) and oncology trial requirements.

• Excellent communication and organizational skills, with the ability to work cross-functionally.

• Detail-oriented with the ability to manage multiple projects in a fast-paced environment.

• Attendance is an essential job function.

This job description does not contain a full listing of activities, duties or responsibilities required of this role. Duties, responsibilities and activities may change, or new ones may be assigned at any time with or without notice.

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