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Clinical Research Practitioner Jobs (NOW HIRING)

Spire Orthopedic Partners

Clinical Research

Wakefield, RI · On-site

$16.25 - $20.30/hr

The Clinical Researcher will develop, implement, and coordinate research and administrative ... Access to a diverse network of practitioners * Broad infrastructure of tools and programs to ...

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How much do clinical research practitioner jobs pay per hour?

As of Aug 17, 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 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.

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.
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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, 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 Sub-Investigator (NP/PA)

ObjectiveHealth

Springboro, OH • Hybrid

Part-time

Re-posted 12 days ago

Job description

Description

Clinical Research Sub-Investigator (NP/PA)

ObjectiveHealth is seeking a licensed Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) to serve as a Sub-Investigator at our Dayton, OH research site. This is a unique opportunity for an advanced practice provider in Internal Medicine, Family Medicine, or a related field to contribute to innovative clinical research while maintaining a flexible schedule. This role is not benefit-eligible; however, it provides a flexible work arrangement and meaningful opportunities for professional growth and development.


Schedule:

  • Part-time
  • Daytime hours
  • 2-3 days/week (flexible days) (onsite)
  • 16-24 hours/week

ObjectiveHealth is a clinical research company transforming how research is conducted at the point of care. Using our proprietary technology, we aim to:

  • Increase patient access to research trials within our communities
  • Provide physicians with enhanced care options for current patients
  • Deliver superior clinical research enrollment metrics to Pharma sponsors

All with the ultimate goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.


Key Responsibilities:

  • Serve as the Sub Investigator for assigned clinical trials, ensuring overall study oversight.
  • Oversee and enforce compliance with study protocols while prioritizing subject safety at all times.
  • Conduct and document physical examinations and medical assessments in accordance with research protocol requirements.
  • Provide continuous medical oversight throughout all phases of the clinical trial lifecycle.
  • Collaborate effectively with study coordinators, site staff, and other research team members to ensure smooth study execution.
  • Participate in sponsor meetings, site initiation visits, monitoring visits, and audits as needed.
  • Maintain strict compliance with GCP, ICH guidelines, FDA regulations, and internal SOPs.

Qualifications:

  • Licensed Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) with an active license in the state of Ohio.
  • Leadership experience in clinical or healthcare settings is preferred.
  • Ability to perform study-related clinical assessments and procedures under the guidance of the Principal Investigator.
  • Strong attention to detail and commitment to maintaining high ethical, clinical, and regulatory standards.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively in a multidisciplinary research environment.


Requirements

This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant

Apply