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Part Time Clinical Trial Management Systems Ctms Jobs

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Clinical Trial Rater

Parsippany, NJ · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Trial Rater

Los Angeles, CA · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Trial Rater

Atlanta, GA · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Trial Rater

Houston, TX · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Trial Rater

New York, NY · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Trial Rater

Boston, MA · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Trial Rater

Durham, NC · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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How much do part time clinical trial management systems ctms jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for part time clinical trial management systems ctms in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What are the most commonly searched types of Clinical Trial Management Systems Ctms jobs?

The most popular types of Clinical Trial Management Systems Ctms jobs are:

Part Time Clinical Trial Management Systems Ctms jobs near you

Endocrinologist - Clinical Research Investigator

ECN Operating LLC

Las Vegas, NV

Part-time, Per diem

Posted 22 days ago

Job description

Position Overview

Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Endocrinologist - Clinical Research Investigator 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).
  • DEA license (preferred).

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