Clinical Research Sub-Investigator (PA or NP)
Bethany MedicalHigh Point, NC
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Overview
Schedule
Full-time
Education
Nursing (RN, LPN)
Career level
Senior-level
Benefits
Health Insurance
Dental Insurance
Vision Insurance
Job Description
“Partnering with patients today for tomorrow’s miracles!”“Established Clinical Research Company is seeking a Clinical Research Sub-Investigator, a Physician Assistant or Nurse Practitioner, to join our team in High Point!”Position SummaryThe Physician Assistant or Nurse Practitioner will serve as a Sub-Investigator on clinical research studies and will work closely with the Principal Investigator and clinical research team to support protocol execution, participant safety, and accurate clinical documentation. This role supports the conduct of clinical trials by performing protocol-required clinical assessments, assisting with participant management, and ensuring compliance with study protocols and regulatory requirements. Prior clinical research experience is not required; training in clinical research processes and Good Clinical Practice (GCP) will be provided.Qualifications and Experience
- Licensed Physician Assistant (PA) or Nurse Practitioner (NP) in good standing.
- Minimum of five (5) years of clinical practice experience in a patient care setting.
- Interest in participating in clinical research and clinical trials.
- Strong clinical assessment, patient management, and documentation skills.
- Ability to work collaboratively with physicians, research coordinators, sponsors, and multidisciplinary teams.
- Excellent communication, organizational, and patient interaction skills.
- Serve as Sub-Investigator on assigned clinical research protocols under the supervision of the Principal Investigator.
- Conduct study-related clinical evaluations, including medical histories, physical examinations, and protocol-required assessments.
- Assess and document adverse events, serious adverse events, and protocol deviations in accordance with study protocols and regulatory requirements.
- Ensure participant safety and protocol compliance during study visits.
- Review and contribute to source documentation and medical record documentation to ensure accuracy and completeness for clinical trials.
- Collaborate with the clinical research coordination team to support participant recruitment, eligibility determination, and completion of study visits.
- Communicate with study sponsors and contract research organizations (CROs) regarding protocol execution, participant status, safety reporting, and study-related questions as appropriate.
- Participate in study-related meetings, monitoring visits, and investigator meetings when required.
- Maintain compliance with Good Clinical Practice (GCP), institutional policies, and regulatory standards related to clinical research.
- Standard working hours: Monday–Friday, 8:00 AM – 5:00 PM.
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FAQs About Clinical Research Sub-Investigator (PA or NP) Jobs at Bethany Medical
What is the work location for this position at Bethany Medical?
This job at Bethany Medical is located in High Point, NC, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Bethany Medical?
Employer has not shared pay details for this role.
What employment applies to this position at Bethany Medical?
Bethany Medical lists this role as a Full-time position.
What experience level is required for this role at Bethany Medical?
Bethany Medical is looking for a candidate with "Senior-level" experience level.
What is the process to apply for this position at Bethany Medical?
You can apply for this role at Bethany Medical either through Sonara's automated application system, which helps you submit applications 10X faster with minimal effort, or by applying manually using the direct link on the job page.