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Cancer Research Manager Jobs (NOW HIRING)

The Oncology Clinical Research Manager also manages regulatory coordinators within the cancer network research program. Works closely with the various Principal Investigators (PIs), Service Line ...

The Oncology Clinical Research Manager also manages regulatory coordinators within the cancer network research program. Works closely with the various Principal Investigators (PIs), Service Line ...

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Cancer Research Manager information

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$50K

$98.6K

$173.5K

How much do cancer research manager jobs pay per year?

As of Jun 7, 2026, the average yearly pay for cancer research manager in the United States is $98,569.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $114,500.00 per year, depending on experience, location, and employer.

What does a Cancer Research Manager do?

A Cancer Research Manager oversees and coordinates cancer research projects, managing teams of scientists and clinicians to ensure studies are conducted efficiently and ethically. They are responsible for developing research protocols, securing funding, ensuring regulatory compliance, and analyzing data. In addition to administrative duties, they often collaborate with other institutions, present findings, and help translate research discoveries into clinical applications that can benefit patients.

What are the main challenges a Cancer Research Manager faces when coordinating multidisciplinary research teams?

As a Cancer Research Manager, coordinating multidisciplinary teams involves balancing diverse expertise and ensuring effective communication across various scientific domains, such as biology, clinical research, and data analysis. Challenges often include aligning different research methodologies, managing timelines, and integrating findings from multiple projects. Successful managers foster collaboration by setting clear goals, facilitating regular updates, and addressing any conflicts promptly, which helps keep research projects on track and promotes innovative solutions to complex cancer-related questions.

What are the key skills and qualifications needed to thrive as a Cancer Research Manager, and why are they important?

To thrive as a Cancer Research Manager, you need advanced knowledge of oncology research, project management expertise, and typically a graduate degree in life sciences or a related field. Familiarity with research protocols, clinical trial management systems, regulatory compliance, and certifications such as Good Clinical Practice (GCP) are essential. Strong leadership, problem-solving abilities, and excellent communication skills help manage research teams and collaborate with stakeholders. These skills ensure effective oversight of complex research projects, regulatory adherence, and advancement of cancer research initiatives.

What is the salary of cancer research?

The salary of a Cancer Research Manager typically ranges from $70,000 to $120,000 annually, depending on experience, location, and the organization. This role often requires strong analytical skills and knowledge of research methodologies.
More about Cancer Research Manager jobs
What cities are hiring for Cancer Research Manager jobs? Cities with the most Cancer Research Manager job openings:
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What states have the most Cancer Research Manager jobs? States with the most job openings for Cancer Research Manager jobs include:
Infographic showing various Cancer Research Manager job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 75% In-person, and 25% Remote job distribution, with an average salary of $98,569 per year, or $47.4 per hour.
Oncology Research Manager

Full-time

Posted yesterday


Job description

Newport News, Virginia
Overview
The Oncology Clinical Research Manager is responsible for leading and managing all RN and non-RN research coordinators across the oncology research program within the Riverside Cancer Care Network. The Oncology Clinical Research Manager also manages regulatory coordinators within the cancer network research program. Works closely with the various Principal Investigators (PIs), Service Line Administrator and Service Line Chief to ensure safety and meet all regulatory, clinical quality and financial requirements of the program. The Oncology Clinical Research Manager is responsible for protocol review, feasibility assessment, contract and budget review and negotiation, and study implementation within the Oncology Research Program. Functions as the clinical expert to manage and lead the clinical research endeavors for Riverside. Collaborates closely with physicians, service line leadership and operational areas for protocol selection and appropriate, targeted growth of the research program. Ensures the research program operates in compliance with principles of Good Clinical Practice and applicable federal, state and local guidelines for research. Responsible for enlisting and maintaining patients on research protocols via direct care coordination or support of other assigned staff responsible for direct care management.
What you will do
  • Manages clinical research operations for all research staff in accordance with federal regulations. Responsible at the administrative level that all research activities are coordinated with all departments within the oncology practices and hospitals. Responsible for coordinating and providing protocol training. Works closely with physicians on facilitating patient recruitment to clinical trials. Maintain established relationships with outside sponsors. Develop new relationships for potential study opportunities.
  • Facilitate/organize department meetings to discuss data, accrual, study patients, and workload. Encourage open discussion and problem solving. Communicates frequently with PIs and provides updates on items such as accrual, patients, SAEs, etc. Open communication with all physicians involved with research and provides support for all research activities. Provide updates to leadership.
  • Supervises research work to include the following but not limited to listed duties - resource to research coordinators, train as needed, work as a coordinator, manage productivity/workload, compliance for studies and regulatory and work closely with physicians for study selection.
  • Ensure budgets are entered in CTMS research software system to facilitate managing study budgets to include coordinating procedure payments, invoices and patient visits. Collaborates with Clinical Research coordinators for accuracy.
  • Collaborates closely with RMG Medical Oncologists, Radiation Oncologists, Surgical Oncologists, Service Line Leadership and other Operational Areas. Maintains frequent open communication with PI on all protocol requirements and regulatory responsibilities. Demonstrates ability to build trusting collaborative relationships with patients and their families to facilitate subject retention. Maintain a professional courteous and considerate demeanor in all interactions with RMG practices, facility and support service team members, research team members, caregivers, patients and visitors. Establish and maintain collaborative relationships with outside Sponsors, CROs, and medical liaisons to identify potential opportunities for growth.
  • Participates in and supports all site auditing/monitoring visits. Maintains protocol regulatory documents in compliance with federal regulations and applicable state regulations. Informs physicians and staff of audit/monitoring results as appropriate

Qualifications
Education
  • Bachelors Degree, BSN (Required)

Experience
  • 2 years experience in Research (Required)
  • 2 years Oncology Research (Preferred)

Skills and Abilities
  • Strong oncology research experience, strong oncology regulatory experience, knowledge of managing regulatory requirements to include: FWAs, NCI experience, pharmaceutical experience, reviewing of consents and making changes as appropriate.
  • Expertise in managing audits to include preparation, site visits, interacting with auditors.
  • Ability to mentor and be a resource to all oncology staff, to include onboarding new team members.
  • Ability to manage data submissions per specific study timelines and accurate data entry.
  • Strong experience in managing and tracking research finances for each specific study, strong written and verbal communication skills.

Licenses and Certifications
  • Certified Oncology Nurse - Oncology Nursing Certification Corporation OCN (Preferred)
  • Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals CCRC, ACRP or Certified Clinical Research Professional within 1 Year(Required)
  • Registered Nurse (RN) - Virginia Department of Health Professions (VDHP) Upon Hire(Required)
  • Valid Drivers License Required

To learn more about being a team member with Riverside Health System visit us at https://www.riversideonline.com/careers.