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Per Diem Sub Investigator information

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How much do per diem sub investigator jobs pay per year?

As of Aug 23, 2026, the average yearly pay for per diem sub investigator in the United States is $75,325.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $98,500.00 per year, depending on experience, location, and employer.

What is the difference between Per Diem Sub Investigator vs Clinical Research Coordinator?

AspectPer Diem Sub InvestigatorClinical Research Coordinator
CredentialsMedical degree or relevant clinical experienceBachelor's degree, often in health or science fields
Work EnvironmentConducts clinical trial visits, reviews data, and ensures protocol complianceManages daily trial operations, patient recruitment, and data collection
Employer & IndustryResearch institutions, hospitals, pharmaceutical companiesResearch sites, hospitals, clinics

Per Diem Sub Investigators typically have medical credentials and focus on overseeing clinical trial protocols, while Clinical Research Coordinators handle daily trial management and patient interactions. Both roles are essential in clinical research but differ in responsibilities and qualifications.

What cities are hiring for Per Diem Sub Investigator jobs?

Cities with the most Per Diem Sub Investigator job openings:

What are the most commonly searched types of Sub Investigator jobs?

The most popular types of Sub Investigator jobs are:

What states have the most Per Diem Sub Investigator jobs?

States with the most job openings for Per Diem Sub Investigator jobs include:

Per Diem Sub Investigator jobs near you

Endocrinologist - Clinical Research Investigator

ECN Operating LLC

Las Vegas, NV • On-site

$120 - $180/hr

Other

Posted 9 days ago

Job description

Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Physician – Endocrinologist to join our expanding team of clinical professionals. The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. This is a part time/per diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies.

Key Responsibilities
  • Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV clinical trials.
  • Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.
  • Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.
  • Provide medical oversight for clinical trial participants, including safety assessments, adverse event evaluations, and ongoing care.
  • Collaborate closely with Clinical Research Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.
  • Review and sign off on source documents, case report forms (CRFs), and regulatory documentation.
  • Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP, FDA, and sponsor requirements.
  • Participate in Site Initiation Visits (SIVs), Monitoring Visits, and Audits as needed.
  • Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.
  • Educate and counsel patients on study procedures, informed consent, and potential side effects.
  • Support recruitment efforts and promote patient retention in trials.
Qualifications
  • MD or DO degree from an accredited medical school.
  • Valid, unrestricted medical license in the state of employment.
  • Board Certified or Board Eligible (BC/BE) in Endocrinology.
  • BC/BE in Family Medicine or Geriatric Medicine will also be considered.
  • Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
  • Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.
Preferred Skills
  • Familiarity with FDA, ICH-GCP, and clinical trial protocols.
  • Experience managing or participating in industry-sponsored clinical trials.
  • Strong attention to detail and ability to document accurately.
  • Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.
  • Ability to work collaboratively with a cross-functional team in a fast-paced research environment.
  • Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).
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