Clinical Research Program Manager Jobs in Indiana

Job Title: Clinical Research Coordinator – Oncology

Job Description

The Clinical Research Coordinator will coordinate oncology clinical trials across phases I–IV, managing a caseload of patients in active treatment and follow-up while supporting the growth of a rapidly expanding cancer research program. This role focuses on patient-facing activities such as screening, recruitment, enrollment, and consenting, as well as close collaboration with nurses, physicians, regulatory teams, data teams, and study sponsors in a fast-paced, team-oriented environment.

Responsibilities

• Coordinate day-to-day activities for a caseload of approximately 7–9 oncology patients in active treatment, as well as patients in follow-up.
• Support the conduct of multiple concurrent clinical trials, including phases I–IV, ensuring adherence to study protocols and timelines.
• Pre-screen patients using medical records and other available data to identify potential candidates for clinical trials.
• Recruit patients for industry-sponsored drug trials by clearly explaining study opportunities and assessing eligibility.
• Obtain informed consent from patients, ensuring they fully understand study procedures, risks, and benefits in accordance with ethical and regulatory standards.
• Collaborate closely with nurses to schedule and support patient visits, including coordinating logistics for clinic days and follow-up appointments.
• Work with physicians and the broader research team to ensure accurate and timely execution of study-related procedures and assessments.
• Partner with regulatory and data teams to support accurate documentation, data integrity, and compliance with regulatory requirements.
• Manage and prioritize work across at least five active trials, adjusting to varying levels of complexity and patient needs.
• Communicate regularly with study sponsors and internal stakeholders to facilitate smooth study operations and address issues as they arise.
• Leverage electronic medical records (EMR) and chart review to track patient status, document trial activities, and maintain accurate records.
• Seek guidance from the Clinical Research Coordinator as needed to resolve complex issues and ensure best practices.
• Contribute to the continued growth and development of the oncology research program and cancer centers by supporting new and ongoing trials.
• Flex schedule as needed to accommodate late patient visits, coordinating with leadership to adjust hours later in the week when necessary.

Essential Skills

• Clinical research experience, with a strong preference for at least 2 years as a Clinical Research Coordinator in oncology.
• Experience with clinical trials across phases I–IV, including industry-sponsored drug trials.
• Phase I drug trial experience; candidates from other therapeutic areas will be considered if they have phase I drug experience.
• At least 2 years of experience obtaining informed consent from patients for clinical trials.
• Demonstrated ability to manage multiple concurrent trials, typically at least five, with varying levels of complexity.
• Hands-on experience with patient pre-screening, recruitment, and enrollment for clinical trials.
• Proficiency in chart review and use of electronic medical records (EMR) in a clinical research setting.
• Experience collaborating with multidisciplinary research teams, including nurses, physicians, regulatory staff, data teams, and sponsors.
• Ability to work effectively in a fast-paced environment while maintaining accuracy and attention to detail.
• Strong communication and interpersonal skills for patient-facing interactions and cross-functional collaboration.

Additional Skills & Qualifications

• Phase I oncology experience is a strong plus.
• Experience with regulatory aspects of clinical trials, including working alongside regulatory teams.
• Experience in oncology research and familiarity with cancer center operations.
• Demonstrated interest in contributing to the growth of a clinical research program and expanding service lines.
• Ability to adapt to evolving responsibilities as new trials open and research sites expand.

Work Environment

The Clinical Research Coordinator will be part of a dedicated oncology research team working primarily onsite at a north campus location, with the expectation of regular travel to an east campus as research activities expand there. Over time, this role will transition to being based full-time at the east location, with the exact timeline to be determined. The schedule follows a structured clinic rhythm: Tuesdays and Thursdays are heavy clinic days focused on patient visits; Mondays and Wednesdays are lighter clinic days; and Fridays are primarily administrative days with the option to work from home, unless an in-person patient visit is required. The environment is fast paced and highly collaborative, involving daily interaction with nurses, physicians, regulatory staff, data teams, and study sponsors, supported by a lead Clinical Research Coordinator for guidance. Occasional late evenings may be needed to accommodate patient visits, with flexibility to shift hours later in the week to maintain work-life balance. The role relies heavily on electronic medical records and standard clinical research tools within a professional oncology clinic and research setting.

This is a Contract to Hire position based out of Indianapolis, IN.

The pay range for this position is $28.00 - $37.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Indianapolis,IN.

This position is anticipated to close on Sep 2, 2026.

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