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Clinical Research Program Manager Jobs in Raleigh, NC

Clinical Program Manager

Durham, NC · On-site

$93K - $285K/yr

We are looking for Senior Project Leaders/Clinical Program Managers to join our innovative and ... Proficient in MS Project is required IQVIA is a leading global provider of clinical research ...

We are looking for Senior Project Leaders/Clinical Program Managers to join our innovative and ... Proficient in MS Project is required IQVIA is a leading global provider of clinical research ...

Clinical Program Manager

Durham, NC · On-site

$93K - $285K/yr

We are looking for Senior Project Leaders/Clinical Program Managers to join our innovative and ... Proficient in MS Project is required IQVIA is a leading global provider of clinical research ...

Responsibilities: 1. Clinical Research Administration Exceeds departmental and organizational goals ... manages change to support program growth, operational efficiency, and high quality research.

Clinical Research Coordinator

Raleigh, NC · On-site

$23.50 - $31.25/hr

Key Responsibilities Coordinate and manage clinical research studies in compliance with study protocols, ICH-GCP guidelines, and applicable regulations. Screen, recruit, and enroll study participants.

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Manage participant reimbursement and study-related communications. * Implement strategies to ... Comprehensive benefits and wellness programs. * The opportunity to make a meaningful impact on ...

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Completion of the DOCR North Carolina state approved Clinical Research Apprenticeship program may ... Must be able to manage, work with, and support multiple stakeholders with different practice styles ...

Showing results 21-40

Clinical Research Program Manager information

See Raleigh, NC salary details

$38.2K

$79.5K

$128.4K

How much do clinical research program manager jobs pay per year?

As of Sep 14, 2026, the average yearly pay for clinical research program manager in Raleigh, NC is $79,527.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,300.00 and $90,200.00 per year, depending on experience, location, and employer.

What does a clinical research program manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

What are the key skills and qualifications needed to thrive as a clinical research program manager?

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.

What are some typical challenges faced by clinical research program managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

What is the difference between Clinical Research Program Manager vs Clinical Research Coordinator?

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Research Program jobs in Raleigh, NC?

The most popular types of Clinical Research Program jobs in Raleigh, NC are:

What are popular job titles related to Clinical Research Program Manager jobs in Raleigh, NC?

For Clinical Research Program Manager jobs in Raleigh, NC, the most frequently searched job titles are:

What cities near Raleigh, NC are hiring for Clinical Research Program Manager jobs?

Cities near Raleigh, NC with the most Clinical Research Program Manager job openings:

Infographic showing various Clinical Research Program Manager job openings in Raleigh, NC as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 72% Full Time, 20% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $79,527 per year, or $38.2 per hour.

Clinical Research Nurse Coordinator, Senior - Duke Cancer Institute

Durham, NC • On-site

Duke University
Colleges, Universities, and Professional Schools • 10K+ employees

$66K - $83K/yr

Full-time

Medical, Dental, Retirement

Posted 13 days ago


Duke University rating

6.7

Company rating: 6.7 out of 10

Based on 55 frontline employees who took The Breakroom Quiz


Job description

School of Medicine:
Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations.
Be You.
The Duke Cancer Institute (DCI) Phase 1 Clinical Research Program is seeking a Clinical Research Nurse Coordinator Sr. to provide leadership for a clinical team conducting multiple complex oncology clinical trials and research studies, including studies involving Investigational Products (IP). In this role, you will play a critical part in advancing innovative cancer treatments while ensuring the highest standards of patient care, research compliance, and study execution.
As a senior clinical research leader, you will partner closely with principal investigators, research staff, sponsors, and multidisciplinary teams to support participant recruitment, study operations, regulatory compliance, financial oversight, and staff development. This role is ideal for an experienced oncology nurse and clinical research professional who is passionate about improving patient outcomes through cutting-edge research and collaborative leadership.
Minimum Requirements
  • Graduation from an accredited BSN, Associate Degree in Nursing, or Nursing Diploma program.
  • Current or compact Registered Nurse (RN) license in the State of North Carolina.
  • Basic Life Support (BLS) certification.
  • Twelve months of appropriate clinical nursing experience.
  • Four years of clinical research experience.
  • Ability to maintain compliance with required hospital, unit, and regulatory training requirements.
  • Knowledge of Good Clinical Practice (GCP), research regulations, and clinical trial operations.

Preferred Qualifications
  • Two years of oncology nursing experience.
  • Two years of clinical research experience in oncology trials.
  • Leadership, supervisory, or management experience.
  • Experience supporting complex clinical trials, including Phase I oncology studies.
  • Experience with study budgets, financial management, and clinical trial closeout activities.
  • Strong communication, mentoring, and problem-solving skills.

Other Requirements
  • Maintain active RN status with the North Carolina Board of Nursing.
  • Maintain required hospital, department, and protocol-specific certifications and training.
  • Ability to work within the professional scope of nursing practice as it relates to clinical research.
  • Ability to oversee and train research staff and nursing personnel.

Be Bold.
Lead Complex Oncology Clinical Trial Operations
  • Direct and oversee day-to-day execution of multiple complex oncology clinical trials and research studies.
  • Coordinate study startup, initiation, enrollment, monitoring, and closeout activities.
  • Partner with principal investigators and study teams to support participant recruitment, enrollment, informed consent, and retention efforts.
  • Identify operational challenges and implement solutions to enhance study performance and participant experiences.

Ensure Research Compliance and Regulatory Excellence
  • Oversee compliance with institutional policies, federal regulations, sponsor requirements, and protocol-specific procedures.
  • Ensure timely documentation and reporting of adverse events, regulatory submissions, enrollment activities, and study records.
  • Maintain oversight of regulatory binders, delegation logs, study training documentation, and participant registration systems.
  • Lead development of Conflict of Interest (COI), Data Safety Monitoring Plans (DSMPs), and Research Data Security Plans (RDSPs).
  • Coordinate external monitoring activities and ensure audit readiness.

Manage Research Finances and Study Resources
  • Monitor study financial milestones, participant reimbursement processes, and research-related expenses.
  • Collaborate with financial teams on budget planning, study forecasting, invoicing, and contract management activities.
  • Lead study budget oversight and financial closeout processes.
  • Ensure appropriate stewardship of research resources and funding.

Develop and Mentor High-Performing Teams
  • Supervise, mentor, and support clinical research staff while fostering a culture of collaboration, accountability, and professional growth.
  • Establish measurable performance goals and provide ongoing coaching and feedback.
  • Coordinate staff assignments, cross-training initiatives, and workforce planning activities.
  • Oversee training, certifications, and competency requirements to ensure compliance with clinical research standards and SOPs.
  • Serve as a subject matter expert and trusted resource for colleagues and research teams.

Promote Data Integrity, Ethics, and Quality
  • Ensure research data are collected, managed, and maintained according to established quality and security standards.
  • Review study documentation and data for completeness, accuracy, and regulatory compliance.
  • Identify data quality concerns and implement corrective actions.
  • Educate study teams on ethical principles, professional standards, and regulations governing clinical research.
  • Uphold Duke's commitment to excellence in patient care, research integrity, and innovation.

Choose Duke.
At the Duke Cancer Institute, you'll join one of the nation's leading academic cancer centers, where groundbreaking research and exceptional patient care come together to transform lives. The Phase 1 Clinical Research Program provides patients access to innovative therapies and first-in-human clinical trials that help shape the future of cancer treatment.
As part of Duke, you'll work alongside nationally recognized physicians, researchers, nurses, and clinical research professionals dedicated to advancing discoveries from the laboratory to the bedside. We foster a culture built on excellence, collaboration, innovation, and compassion while supporting the professional growth and development of our team members.
Job Code: 00001204 CLINICAL RESEARCH NURSE COORDINATOR, SR
Job Level: 55
Anticipated Pay Range: Duke University provides an annual base salary range for this position as USD $78,347.00to USD $133,188.00. Duke University considers factors such as (but not limited to) scope and responsibilities of the position; candidate's work experience, education/training, and key skills; internal peer equity; as well as market and organizational considerations when extending an offer.
Your total compensation goes beyond the dollars on your paycheck. Duke provides comprehensive and competitive medical and dental care programs, generous retirement benefits, and a wide array of family-friendly and cultural programs to eligible team members. Learn more at: https://hr.duke.edu/benefits/
Equal Opportunity Employer: Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex (including pregnancy and pregnancy- related conditions), sexual orientation, or military status.
Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas-an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values.
Essential Physical Job Functions:
Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and reasonable accommodation(s) can be requested with Duke Access and Accommodations Services (email: DAAS@duke.edu; phone: 919-668-1267).

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About Duke University

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Duke is regarded as one of America's leading research universities. Located in Durham, North Carolina, Duke is positioned in the heart of the Research Triangle, which is ranked annually as one of the best places in the country to work and live. Duke has more than 15,000 students who study and conduct research in its 10 undergraduate, graduate, and professional schools. With about 40,000 employees, Duke is the third largest private employer in North Carolina, and it now has international programs in more than 150 countries.

Industry

Colleges, universities, and professional schools and hospitals

Company size

10,000+ Employees

Headquarters location

Durham, NC, US