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Part Time Clinical Research Monitor Jobs in Silver Spring, MD

Medix

Clinical Research Nurse

Baltimore, MD · On-site

$31.73 - $42.31/hr

Plan and implement clinical research protocols, including data collection systems and study ... Assess opioid withdrawal using standardized scales and conduct monitoring and documentation.

IQVIA

Clinical Trial Psych Rater

Fairfax, VA · Remote

$62K - $156K/yr

Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Trial Rater

Washington, DC · Remote

... clinical research services. We collaborate with top pharmaceutical and biotech companies to ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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Part Time Clinical Research Monitor information

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$5

$41

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

As of Sep 5, 2026, the average hourly pay for part time clinical research monitor in Silver Spring, MD is $40.01, according to ZipRecruiter salary data. Most workers in this role earn between $39.52 and $40.53 per hour, depending on experience, location, and employer.

What is a part time clinical research monitor?

Part time clinical research monitors are professionals who oversee the conduct of clinical trials on a part-time basis. Their primary role is to ensure that research studies comply with regulatory standards, protocols, and ethical guidelines while monitoring participant safety and data integrity. They may visit research sites, review documentation, verify data accuracy, and communicate with investigators, but work fewer hours than full-time monitors. This role is ideal for individuals seeking flexible schedules or supplementary income in the clinical research field.

How do part time clinical research monitors balance workload and ensure data quality across multiple studies?

Part-time clinical research monitors often manage their time across several studies by prioritizing tasks, maintaining clear communication with site staff, and using detailed tracking systems. They may face challenges in staying updated on protocol amendments and ensuring timely site visits due to limited hours. To maintain data quality, they frequently collaborate with full-time monitors, utilize remote monitoring tools, and keep thorough documentation. Regular check-ins with the research team help address any issues promptly and ensure compliance with regulatory standards.

What are the key skills and qualifications needed to thrive as a part time clinical research monitor?

To thrive as a Part Time Clinical Research Monitor, you need a solid understanding of clinical trial protocols, GCP guidelines, and typically a degree in a health-related field. Familiarity with electronic data capture (EDC) systems, regulatory documentation, and possibly certifications like ACRP or SOCRA is advantageous. Strong attention to detail, effective communication, and organizational skills help you manage site visits and collaborate with research teams. These skills ensure protocol compliance, data integrity, and the ethical conduct of clinical studies.

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

AspectPart Time Clinical Research MonitorPart Time Clinical Trial Coordinator
CredentialsTypically requires life sciences degree, certification (e.g., CCRP), and monitoring experienceUsually requires a degree in health sciences or related field, with project management skills
Work EnvironmentMonitors clinical sites remotely or on-site, ensuring compliance with protocolsCoordinates trial activities, manages documentation, and communicates with sites and sponsors
Employer & Industry UsageCommonly employed by CROs, pharmaceutical companies, and research institutionsEmployed by research sites, hospitals, or sponsors to oversee trial logistics

While both roles support clinical trials, the Part Time Clinical Research Monitor focuses on compliance and monitoring site activities, whereas the Part Time Clinical Trial Coordinator manages trial logistics and documentation. Understanding these differences helps in choosing the right career path or job search focus.

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

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

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

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

Part Time Clinical Research Monitor jobs near you

Part-time or Full-time Physician - Clinical Research

Headlands Research

Baltimore, MD • On-site

Full-time, Part-time

Re-posted 15 days ago

Job description

Pharmasite Research, located in the greater Baltimore area, is a dedicated clinical research site with over twenty years of experience across multiple therapeutic areas, with a particular focus on mental health and central nervous system (CNS) conditions. The site is committed to delivering high-quality, patient-centered research, prioritizing participant care, safety, and study integrity. With an experienced team serving a diverse population, Pharmasite Research partners with sponsors and CROs to advance innovative therapies and improve health outcomes.

Championing Diversity in Clinical Trials

Diversity isn't just a checkbox for us-it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.

The Role of a Lifetime

Are you ready to make a difference? With ample support and a culture of collaboration, you'll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands. 

Responsibilities:

  • Lead and oversee clinical trials, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
  • Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
  • Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
  • Obtain IRB approval for study initiation and any protocol modifications.
  • Oversee subject safety, trial conduct compliance, and the informed consent process.
  • Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
  • Provide ongoing training and support to research staff.

Requirements:

  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without.
  • Current and unencumbered license to practice as an MD or DO within the state of Maryland required (or eligible for).
  • Must be board-certified or board-eligible.
  • Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
  • Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.

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