ZipRecruiter

Log In

2

Part Time Duke Clinical Research Jobs in Silver Spring, MD

IQVIA

Freelance Independent Rater

Washington, DC · Remote

$62K - $156K/yr

... clinical research services, commercial insights and healthcare intelligence to the life sciences ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Freelance Independent Rater

Washington, DC · Remote

$62K - $156K/yr

... clinical research services, commercial insights and healthcare intelligence to the life sciences ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

BCC - LH

QA Specialist

Bethesda, MD · On-site

This opportunity is part-time with BCC and it is on-site in Bethesda, MD and/or remote. Position ... facilitates new research efforts, clinical studies, or other initiatives. Evaluates the ...

BCC - LH

QA Specialist

Bethesda, MD

This opportunity is part-time with BCC and it is on-site in Bethesda, MD and/or remote. Position ... facilitates new research efforts, clinical studies, or other initiatives. Evaluates the ...

previous pagenext page

Showing results 21-40

All JobsDuke Clinical Research JobsPart Time Duke Clinical Research JobsPart Time Duke Clinical Research Jobs in Silver Spring, MD

Part Time Duke Clinical Research information

See Silver Spring, MD salary details

$19

$31

$44

How much do part time duke clinical research jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for part time duke clinical research in Silver Spring, MD is $31.18, according to ZipRecruiter salary data. Most workers in this role earn between $26.59 and $33.03 per hour, depending on experience, location, and employer.

What is the difference between Part Time Duke Clinical Research vs Part Time Clinical Research Coordinator?

AspectPart Time Duke Clinical ResearchPart Time Clinical Research Coordinator
Required CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusUsually requires a bachelor's degree; certifications like CCRP or CCRC are common
Work EnvironmentConducts research at Duke University or affiliated sites, often in academic or hospital settingsWorks in hospitals, clinics, or research sites, often in academic or healthcare environments
Employer & Industry UsagePrimarily employed by Duke University or research institutions involved in clinical trialsEmployed by hospitals, research organizations, or academic institutions conducting clinical studies

Both roles involve coordinating clinical research activities, but Part Time Duke Clinical Research is specific to Duke University and may involve more academic research settings, while Part Time Clinical Research Coordinator is broader across various healthcare and research organizations.

What are the most commonly searched types of Duke Clinical Research jobs in Silver Spring, MD?

The most popular types of Duke Clinical Research jobs in Silver Spring, MD are:

What are popular job titles related to Part Time Duke Clinical Research jobs in Silver Spring, MD?

For Part Time Duke Clinical Research jobs in Silver Spring, MD, the most frequently searched job titles are:

What job categories do people searching Part Time Duke Clinical Research jobs in Silver Spring, MD look for?

The top searched job categories for Part Time Duke Clinical Research jobs in Silver Spring, MD are:

What cities near Silver Spring, MD are hiring for Part Time Duke Clinical Research jobs?

Cities near Silver Spring, MD with the most Part Time Duke Clinical Research job openings:

Part Time Duke Clinical Research jobs near you

Sub-Investigator

Patient First Clinical Trials LLC

Lutherville Timonium, MD • On-site

$55 - $65/hr

Part-time

Re-posted 14 days ago

Job description

About PFCTrials

Patients First Clinical Trials (PFCTrials) is a community-focused, patient-centric research site connecting diverse patient populations with innovative clinical trials. Our mission is to advance patient care through high-quality, ethical research while fostering strong relationships with local healthcare providers and the community.

Position Summary

PFCTrials is seeking an experienced Sub-Investigator (MD, DO, or NP) with strong clinical and patient care experience to provide medical oversight, support patient care, ensure protocol adherence, and collaborate with the study team. This role is ideal for clinicians who want to participate in research while maintaining direct patient care involvement.

Key Responsibilities

Clinical Oversight

  • Assist the Principal Investigator in protocol implementation and study oversight.
  • Conduct study-related procedures such as patient assessments, including medical history, physical exams (as within scope of practice), medical rating scales and adverse event evaluation.
  • Ensure participant safety, monitor protocol adherence, and make medically appropriate decisions.

Patient Care & Engagement

  • Build rapport with participants and provide guidance throughout the study.
  • Obtain informed consent and clearly explain study procedures.
  • Implement strategies to maximize participant retention and adherence.

Regulatory Compliance & Documentation

  • Ensure all study activities comply with GCP, FDA, and IRB requirements.
  • Review source documents and eCRFs for accuracy and completeness.
  • Assist with monitoring visits, audits, and inspections.

Collaboration

  • Work closely with the Principal Investigator, Research Coordinator, and study staff.
  • Provide mentorship and guidance on clinical aspects of trials.
  • Collaborate with sponsors and CROs as needed.

Must-Have Qualifications

  • MD, DO, or Nurse Practitioner (NP) license eligible to serve as Sub-Investigator.
  • Minimum 3+ years of clinical/patient care experience in fast-paced clinical setting.
  • Strong clinical judgment and decision-making skills.
  • Excellent communication and interpersonal skills for patient and team interactions.

Nice-to-Have Qualifications

  • Prior Sub-Investigator or research experience.
  • Familiarity with EDC/CTMS and clinical trial documentation.
  • Commitment to community engagement and diverse patient recruitment.
  • Mentoring or supervisory experience.

Why PFCTrials?

  • Participate in high-impact, patient-centered clinical trials.
  • Work in a flexible, mission-driven environment.
  • Opportunities for professional growth and involvement across multiple therapeutic areas.

Job Types: Part-time, Contract

Work Location: In person