ZipRecruiter

Log In

1

Clinical Research Practitioner Jobs (NOW HIRING)

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 ...

next page

Showing results 1-20

All JobsClinical Research Practitioner Jobs

Clinical Research Practitioner information

See salary details

$16

$72

$131

How much do clinical research practitioner jobs pay per hour?

As of Aug 16, 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.

Is a Clinical Research Practitioner a good career?

A Clinical Research Practitioner is a valuable role in healthcare and medical research, involving managing clinical trials, ensuring compliance, and collecting data. It offers opportunities for specialization, requires knowledge of regulations and good communication skills, and can lead to advancement in the research field.

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.
More about Clinical Research Practitioner jobs

What states have the most Clinical Research Practitioner jobs?

States with the most job openings for Clinical Research Practitioner jobs include:

What job categories do people searching Clinical Research Practitioner jobs look for?

The top searched job categories for Clinical Research Practitioner jobs are:

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, 72% Full Time, 17% 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.

Clinical Research Nurse Practitioner

Monroe Biomedical Research

Louisville, KY • On-site

Full-time

Medical, Dental, Vision

Posted 9 days ago

Job description

MBR - Louisville, KY | Onsite
ABOUT THE ROLE
Monroe Biomedical Research is growing, and we are seeking an experienced, patient-focused Clinical Research Nurse Practitioner to join our Louisville team.
This unique role combines advanced clinical practice with hands-on clinical research coordination. The Clinical Research Nurse Practitioner will work directly with study participants while supporting the successful execution of clinical trials from patient screening and study visits through documentation and follow-up.
This is an excellent opportunity for an NP who enjoys direct patient care, thrives in a fast-paced clinical environment, and is interested in contributing to research that advances medicine and expands treatment options for patients.
WHAT YOU'LL DO
Clinical Research & Study Management
• Coordinate and manage clinical trial visits from screening through study completion
• Review study protocols and ensure required procedures and assessments are completed accurately and within protocol-defined timelines
• Develop and maintain accurate and complete source documentation in accordance with study protocols
• Support participant screening, enrollment, and ongoing study activities
• Work closely with investigators, sponsors, monitors, and internal research staff to support successful study execution
• Ensure clinical trials are conducted in accordance with Good Clinical Practice (GCP), FDA regulations, sponsor requirements, and internal procedures.
Patient Care & Clinical Responsibilities
• Provide clinical assessment and care to adult study participants within the scope of NP practice and study protocol requirements
• Perform and/or oversee study-related clinical procedures, including blood draws, ECGs, pulmonary function testing, vital signs, and other protocol-required assessments
• Review relevant medical history, medications, laboratory results, and other clinical information
• Educate participants regarding study requirements, procedures, medications, and follow-up expectations
• Identify and communicate changes in participant condition, adverse events, or other clinically significant findings to appropriate study team members
• Provide a professional, compassionate, and supportive experience throughout each participant's clinical trial journey.
Data, Documentation & Quality
• Review and process medical records and study-related clinical documentation
• Accurately document study visits and clinical findings
• Enter and maintain study data in sponsor and clinical research systems accurately and within required timelines
• Prepare, process, and coordinate shipment of laboratory specimens according to protocol requirements
• Respond to data queries and assist with maintaining complete, inspection-ready study records
QUALIFICATIONS
• Current Nurse Practitioner (NP) licensure with the ability to practice with an adult patient population
• Master's degree in Nursing or related advanced practice field required
• Previous experience providing direct patient care required
• Clinical research experience strongly preferred
• Strong clinical judgment and commitment to patient safety
• Excellent attention to detail, organization, and documentation skills
• Ability to interpret and follow detailed clinical trial protocols
• Ability to effectively manage competing priorities and multiple studies in a fast-paced research environment
• Strong communication and interpersonal skills with a patient-centered approach
WHY JOIN MONROE BIOMEDICAL RESEARCH?
• Join a growing clinical research organization contributing to the advancement of new treatments and therapies
• Work alongside a collaborative and supportive multidisciplinary research team
• Gain exposure to a diverse portfolio of clinical trials
• Opportunity to combine advanced clinical skills with clinical research experience
• 100% company-paid employee Health, Dental, and Vision insurance

Apply