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How much do cancer research consultant jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for cancer research consultant in the United States is $39.38, according to ZipRecruiter salary data. Most workers in this role earn between $31.01 and $48.08 per hour, depending on experience, location, and employer.

What does a cancer research consultant do?

A Cancer Research Consultant provides expert guidance and advice to organizations, research teams, or pharmaceutical companies involved in cancer research. They help design studies, interpret data, and develop strategies for clinical trials or research projects. Their role often includes staying current on scientific advancements, ensuring compliance with regulations, and optimizing research processes to improve outcomes. They may also assist with grant applications, publications, and collaborations among stakeholders.

What are the key skills and qualifications needed to thrive as a cancer research consultant?

To thrive as a Cancer Research Consultant, you need advanced knowledge in oncology, research methodologies, and data analysis, typically supported by a graduate degree (PhD or MD) in a relevant field. Expertise in clinical trial design, statistical software (such as SPSS or SAS), and familiarity with regulatory requirements like GCP are commonly required. Strong communication, problem-solving, and project management skills help consultants effectively translate research findings and collaborate with multidisciplinary teams. These skills and qualities are crucial for driving impactful cancer research and ensuring that projects meet scientific, ethical, and regulatory standards.

What are some common challenges faced by cancer research consultants when managing multidisciplinary projects?

Cancer Research Consultants often work with diverse teams comprising clinicians, laboratory scientists, data analysts, and regulatory specialists. Coordinating between these groups can be challenging due to differing priorities, communication styles, and timelines. Effective consultants need strong project management and interpersonal skills to facilitate collaboration, ensure everyone stays aligned on goals, and address any conflicts that arise. Being proactive in communication and setting clear expectations helps overcome these challenges and leads to successful project outcomes.

Are cancer research consultants paid well?

Cancer research consultants typically earn competitive salaries that reflect their specialized knowledge and experience in oncology research. Compensation varies based on factors such as education, certifications, location, and years of experience, with many earning above average for research roles. They often work in academic, clinical, or industry settings, where salaries can range from moderate to high depending on the complexity of projects and responsibilities.

How do I become a cancer research consultant?

To become a cancer research consultant, typically a candidate needs a master's or doctoral degree in a relevant field such as oncology, biology, or medical research. Gaining experience through research positions, developing strong analytical and communication skills, and staying updated on current cancer treatments and research methods are essential steps. Certifications or specialized training in clinical research can also enhance qualifications.

What is a cancer research consultant?

A cancer research consultant is a professional who provides expertise in designing, analyzing, and interpreting cancer studies. They often work with research teams, utilize statistical tools, and may hold advanced degrees in fields like oncology, biology, or public health to support cancer research projects.

What are popular job titles related to Cancer Research Consultant jobs?

For Cancer Research Consultant jobs, the most frequently searched job titles are:

Infographic showing various Cancer Research Consultant job openings in the United States as of September 2026, with employment types broken down into 82% Full Time, and 18% Part Time. Highlights an 88% In-person, 6% Hybrid, and 6% Remote job distribution, with an average salary of $81,905 per year, or $39.4 per hour.

Clinical Research Study Manager - Oncology

Somerset, NJ • On-site

Vitalief
Health Care and Social Assistance • 51 - 200 employees
Learn more about Vitaliefexternal

$115K - $145K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 13 days ago

Key responsibilities

  • Oversee the successful execution of Phase II-IV oncology clinical trials, including protocol implementation, study activation, enrollment, data collection, and research workflows.

  • Lead daily oncology clinical research operations across two locations and supervise, mentor, and develop a small clinical research team.

  • Ensure compliance with GCP, FDA regulations, OHRP, NIH, HIPAA, and IRB requirements, and oversee regulatory submissions, documentation, record retention, and reporting of protocol deviations.

Job description

ABOUT VITALIEF
Vitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative Consulting and Functional Service Provider (FSP) solutions to academic medical centers, health systems, sponsors, CROs, and site networks.  By combining deep subject matter expertise with the experience of senior research practitioners, we help organizations accelerate study activation, optimize operations, improve financial performance, and build scalable workforce solutions that reduce costs, increase efficiency, and advance clinical breakthroughs for patients.
POSITION SUMMARY
Vitalief is seeking an experienced Clinical Research Study Manager to join our team as a full-time employee supporting interventional oncology clinical trials at a premier research center in Somerset, NJ.  In this highly visible role, you will oversee the successful execution of Phase II–IV oncology clinical trials, spanning multiple oncology disease groups, including Breast, GI/GU, Head & Neck, and Lung cancers.
The ideal candidate thrives in a fast-paced, high-volume clinical research environment and is passionate about advancing cancer research while ensuring operational excellence, regulatory compliance, and the successful delivery of complex clinical trials.
WHY VITALIEF?
  • Meaningful Impact: Support innovative oncology research that advances treatment options and improves patient outcomes.
  • People-First Culture: Join a collaborative environment focused on professional growth, innovation, and teamwork.
  • Comprehensive Benefits: Enjoy 20 PTO days, 9 paid holidays, company-paid life insurance, short- and long-term disability coverage, a 401(k) retirement plan, and comprehensive healthcare benefits.
  • Work Location: Four (4) days on site in Somerset, NJ and one (1) day on site in Hamilton, NJ per week.
  • Schedule: Monday through Friday, 8:00 AM – 4:30 PM.
  • Salary Range: $115,000 to $145,000 depending on experience.

RESPONSIBILITIES
  • Lead daily oncology clinical research operations across two locations.
  • Oversee protocol implementation, study activation, enrollment, data collection, and research workflows.
  • Supervise, mentor, and develop a small clinical research team.
  • Support recruitment, onboarding, performance management, competency assessments, and professional development.
  • Ensure compliance with GCP, FDA regulations, OHRP, NIH, HIPAA, and IRB requirements.
  • Oversee regulatory submissions, documentation, record retention, and reporting of protocol deviations.
  • Develop corrective and preventive action plans to support continuous improvement.
  • Partner with investigators, research leadership, clinical teams, and institutional stakeholders to support research goals and priorities.
  • Participate in operational planning, resource management, and process improvement initiatives.
  • Lead meetings and multidisciplinary collaborations to enhance research performance and patient access to clinical trials.

QUALIFICATIONS
  • Bachelor’s degree in Nursing, Health Sciences, Life Sciences, Public Health, or related field required; Master’s degree preferred.
  • Minimum of 3 years of oncology clinical research experience, including experience managing clinical trials.
  • Minimum of 1 to 2 years of supervisory or management experience within a clinical research environment.
  • Registered Nurse (RN) preferred.
  • Experience working in an academic medical center, cancer center, or large healthcare system preferred.
  • Knowledge of oncology clinical trial operations, protocol implementation, regulatory requirements, and research compliance standards, including GCP, FDA, OHRP, NIH, HIPAA, and IRB requirements.
  • Demonstrated ability to lead, mentor, and develop research teams in a complex clinical environment.
  • Strong project management, organizational, and time management skills with the ability to manage multiple priorities.
  • Experience with quality assurance activities, auditing, process improvement, and operational optimization.
  • Proficiency with Microsoft Office and clinical research systems, including CTMS, EDC platforms, and/or OnCore.
  • Excellent written, verbal, and interpersonal communication skills with the ability to collaborate effectively with physicians, research teams, and cross-functional stakeholders.
  • Strong critical thinking, problem-solving, decision-making, and relationship-building abilities.

PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing.
IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.
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