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How much do clinical research practitioner jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical research practitioner in the United States is $72.98, according to ZipRecruiter salary data. Most workers in this role earn between $59.13 and $74.76 per hour, depending on experience, location, and employer.

What is a clinical research practitioner?

A Clinical Research Practitioner is a professional who supports the delivery and management of clinical research studies within healthcare settings, such as hospitals or research institutes. They assist with tasks like recruiting participants, collecting data, and ensuring research protocols are followed. While they may not be medically qualified, they play a vital role in making sure clinical trials run smoothly and ethically. Their work helps advance medical knowledge and improve patient care by contributing to the development of new treatments and therapies.

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

To thrive as a Clinical Research Practitioner, you need a solid background in life sciences or healthcare, understanding of clinical trial protocols, and typically a degree in a relevant field. Proficiency with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of Good Clinical Practice (GCP) guidelines or certification is often required. Attention to detail, strong organizational skills, and effective communication are essential soft skills for collaborating with research teams and participants. These competencies ensure the integrity of clinical studies, regulatory compliance, and the successful advancement of medical research.

What are some typical challenges a clinical research practitioner may face when coordinating clinical trials?

Clinical Research Practitioners often encounter challenges such as balancing strict protocol adherence with patient care, managing complex documentation requirements, and ensuring timely recruitment of suitable participants. Coordinating between multidisciplinary teams—such as investigators, nurses, and data managers—requires strong communication and organizational skills. Additionally, practitioners must stay current with regulatory changes and ethical guidelines to ensure compliance throughout all trial phases.

How do you become a clinical research practitioner?

To become a clinical research practitioner, individuals typically need a bachelor's degree in a health-related field such as nursing, biology, or pharmacy. Relevant skills include knowledge of clinical trial protocols, good communication, and attention to detail; certifications like Certified Clinical Research Professional (CCRP) can enhance job prospects. Experience in healthcare or research settings is also valuable for entry into this role.

Is clinical research in high demand?

Clinical research practitioners are in high demand due to the ongoing need for new medical treatments and advancements in healthcare. The field offers growth opportunities, especially for those with strong organizational skills and knowledge of Good Clinical Practice (GCP) guidelines, as clinical trials continue to expand globally.
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Clinical Research Practitioner jobs near you
Infographic showing various Clinical Research Practitioner job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $151,807 per year, or $73 per hour.

Senior Clinical Research Coordinator - Oncology

Vitalief

Newark, NJ • On-site

$75K - $85K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 9 days ago

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 Senior Clinical Research Coordinator (CRC) to join our team as a full-time employee with a comprehensive benefits package. This role will support a portfolio of Phase II-IV oncology interventional clinical trials at a community hospital site in Newark, NJ.
The ideal candidate will have a minimum of three years of clinical research coordination experience, a strong background supporting oncology trials across multiple disease areas, experience mentoring junior CRC team members, and the ability to excel in a collaborative, small-team environment.
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: Fully on site in Newark, NJ for the first 3 months. Following training, transition to a hybrid schedule of 4 days onsite and 1 remote day per week.
  • Schedule: Monday through Friday, 8:00 AM - 4:30 PM.
  • Salary Range: $75,000 to $85,000 depending on experience.

RESPONSIBILITIES
  • Support the execution of Phase II-IV oncology clinical trials, including pharmaceutical-sponsored, ECOG, and investigator-initiated studies.
  • Manage trials across multiple oncology disease groups, including GYN, Breast, GI/GU, Head & Neck, and Lung cancers.
  • Oversee a portfolio of approximately 15-20 active clinical trials in a fast-paced, high-volume clinical environment.
  • Identify and screen potential study participants using physician schedules, pathology reports, multidisciplinary tumor boards, referrals, and other clinical resources.
  • Obtain informed consent and enroll eligible patients in accordance with protocol requirements and regulatory standards.
  • Manage patients throughout the clinical trial lifecycle, from consent through completion of active treatment.
  • Educate patients regarding study procedures, treatment schedules, and protocol requirements.
  • Coordinate patient care activities with physicians, infusion teams, nursing staff, radiology, pathology, laboratories, and other clinical departments.
  • Monitor patient safety, document clinical outcomes, and ensure timely reporting of adverse events and Serious Adverse Events (SAEs).
  • Maintain accurate clinical trial documentation, source records, regulatory files, patient calendars, and study-related documentation.
  • Ensure compliance with study protocols, Good Clinical Practice (GCP), institutional policies, and regulatory requirements.
  • Provide guidance and mentorship to junior CRC team members and support team collaboration.

QUALIFICATIONS
  • Bachelor's degree in health science, life science, nursing, or a related field.
  • Minimum of 3 years of clinical research coordination experience supporting interventional Phase II-IV clinical trials.
  • Required oncology clinical trial experience, preferably with exposure to multiple oncology disease areas.
  • Experience with patient identification, pre-screening, informed consent, enrollment, retention, regulatory compliance, and clinical data management.
  • Prior experience mentoring or supporting the development of junior CRCs.
  • Proficiency with EPIC and OnCore™ CTMS.
  • Ability to manage multiple concurrent studies while maintaining strong attention to detail and organization.
  • Adaptable, solutions-oriented mindset with the ability to work effectively in a small, collaborative team environment.
  • Strong interpersonal and communication skills with the ability to work closely with physicians, nurses, research staff, hospital departments, and external partners.
  • Experience ensuring SAEs are documented, completed, and reported within protocol-defined timelines.
  • Proficiency with Microsoft Office applications and clinical research systems.

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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