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Clinical Research Practitioner Jobs (NOW HIRING)

Monroe Biomedical Research, LLC

$18 - $23.75/hr

This is an excellent opportunity for an RN or NP who enjoys patient care, thrives in a fast‑paced ... Clinical Research & Study Management * Coordinate clinical trial visits from screening through ...

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

By combining deep subject matter expertise with the experience of senior research practitioners, we ... POSITION SUMMARY: We are seeking an experienced Clinical Research Coordinator (CRC) to join ...

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

By combining deep subject matter expertise with the experience of senior research practitioners, we ... POSITION SUMMARY: We are seeking an experienced Clinical Research Coordinator (CRC) to join ...

IMA Clinical Research, Inc.

$130K - $150K/yr

Psychiatric Nurse Practitioner (PMHNP) or Physician Assistant - Clinical Research Chicago, IL | Full-Time | Monday-Friday Bring your psychiatric expertise to clinical research. Join IMA Clinical ...

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How much do clinical research practitioner jobs pay per hour?

As of Sep 14, 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 September 2026, with employment types broken down into 3% As Needed, 73% Full Time, 16% Part Time, and 8% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $151,807 per year, or $73 per hour.

Clinical Research Coordinator

Monroe, NC • On-site

Monroe+Biomedical+Research
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$22.50 - $30/hr

Other

Re-posted 28 days ago

Job description

ABOUT THE ROLE:

Monroe Biomedical Research is seeking an experienced, patient-focused onsite Clinical Research Coordinator preferably with their (RN/NP) to join our Monroe, NC location.

This hands-on role combines direct patient care with clinical research coordination. The Clinical Research Nurse will support participants throughout the clinical trial process, from screening and study visits through procedures, documentation, and follow-up.

This is an excellent opportunity for an RN or NP who enjoys patient care, thrives in a fast-paced environment, and wants to contribute to research that advances medicine and expands treatment options.

WHAT YOU’LL DO: Clinical Research & Study Management
  • Coordinate clinical trial visits from screening through completion.
  • Review protocols and ensure study procedures are completed accurately and on schedule.
  • Maintain complete and accurate source documentation.
  • Support participant screening, enrollment, and ongoing study activities.
  • Collaborate with investigators, sponsors, monitors, and research staff.
  • Ensure compliance with GCP, FDA regulations, sponsor requirements, and internal procedures.
Patient Care & Clinical Responsibilities
  • Provide clinical assessment and care to adult study participants within your scope of practice and study requirements.
  • Perform and/or oversee procedures including:
    • Blood draws/phlebotomy
    • ECGs
    • Pulmonary function testing
    • Vital signs
    • Other protocol-required assessments
  • Review medical history, medications, laboratory results, and other clinical information.
  • Educate participants on study procedures, medications, and follow-up.
  • Recognize and communicate adverse events or clinically significant findings.
  • Deliver a professional, compassionate, and patient-centered experience.
Data & Documentation
  • Document study visits, clinical findings, and patient information accurately.
  • Enter and maintain study data within sponsor systems and required timelines.
  • Process and coordinate laboratory specimens according to protocol.
  • Respond to data queries and maintain accurate, inspection-ready records.
QUALIFICATIONS:
  • Current RN or NP license with the ability to practice with an adult patient population.
  • Bachelor’s degree in nursing required; Master’s degree for NP candidates.
  • Previous direct patient care experience required.
  • Clinical research experience is highly preferred.
  • Strong clinical judgment and commitment to patient safety.
  • Excellent organization, documentation, and attention to detail.
  • Ability to interpret and follow detailed clinical trial protocols.
  • Ability to manage multiple priorities in a fast-paced environment.
  • Strong communication and interpersonal skills.
  • Professional, compassionate, and patient-focused approach.
  • Must commute daily to Monroe, NC daily.
WHY JOIN MONROE BIOMEDICAL RESEARCH?
  • Join a growing clinical research organization.
  • Combine patient care with innovative clinical research.
  • Contribute directly to medical advancements and emerging treatments.
  • Work with a collaborative, mission-driven team.
  • Gain experience across a variety of clinical studies.
  • Build opportunities for professional growth and leadership.
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