Research Program Manager - Oncology
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Overview
Schedule
Full-time
Education
Nursing (RN, LPN)
Career level
Director
Remote
On-site
Compensation
$115,000-$145,000/year
Benefits
Health Insurance
Disability Insurance
Life Insurance
Job Description
ABOUT VITALIEFVitalief 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 SUMMARYVitalief is seeking an experienced Clinical Research Program 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.
- 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.
- 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.
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FAQs About Research Program Manager - Oncology Jobs at Vitalief
What is the work location for this position at Vitalief?
This job at Vitalief is located in Somerset, NJ, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Vitalief?
Candidates can expect a pay range of $115,000 and $145,000 per year.
What employment applies to this position at Vitalief?
Vitalief lists this role as a Full-time position.
What experience level is required for this role at Vitalief?
Vitalief is looking for a candidate with "Director" experience level.
What education level is required for this job?
The education requirement for this position is Nursing (RN, LPN). Candidates with relevant qualifications or equivalent experience may also be considered.
What benefits are offered by Vitalief for this role?
Vitalief offers following benefits: Health Insurance, Disability Insurance, Life Insurance, Paid Holidays, Paid Vacation, 401k Matching/Retirement Savings, and Health & Wellness Programs for this position. Actual benefits may vary depending on the employer's policies and employment terms.
What is the process to apply for this position at Vitalief?
You can apply for this role at Vitalief either through Sonara's automated application system, which helps you submit applications 10X faster with minimal effort, or by applying manually using the direct link on the job page.