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Part Time Clinical Research Monitor Jobs in Silver Spring, MD

Proud Moments

BCBA In Home - $20,000 Bonus

Fairfax, VA · On-site

$75K - $92K/yr

... or part-time clinical experts. As a Proud Moments BCBA, you'll enjoy professional respect ... Advocate for your clients by monitoring for potential issues and communicating concerns * Share ...

Proud Moments

In-Home Based BCBA

Germantown, MD · On-site

$100K - $115K/yr

... or part-time clinical experts. As a Proud Moments BCBA, you'll enjoy professional respect ... Advocate for your clients by monitoring for potential issues and communicating concerns * Share ...

Proud Moments

BCBA In Home - $20,000 Bonus

Fairfax, VA · On-site

$75K - $92K/yr

... or part-time clinical experts. As a Proud Moments BCBA, you'll enjoy professional respect ... Advocate for your clients by monitoring for potential issues and communicating concerns * Share ...

Proud Moments

BCBA In Home - $20,000 Bonus

Falls Church, VA · On-site

$79K - $96K/yr

... or part-time clinical experts. As a Proud Moments BCBA, you'll enjoy professional respect ... Advocate for your clients by monitoring for potential issues and communicating concerns * Share ...

Proud Moments

BCBA In Home - $20,000 Bonus

Fairfax, VA · On-site

$75K - $92K/yr

... or part-time clinical experts. As a Proud Moments BCBA, you'll enjoy professional respect ... Advocate for your clients by monitoring for potential issues and communicating concerns * Share ...

Proud Moments

BCBA In Home - $20,000 Bonus

Falls Church, VA · On-site

$79K - $96K/yr

... or part-time clinical experts. As a Proud Moments BCBA, you'll enjoy professional respect ... Advocate for your clients by monitoring for potential issues and communicating concerns * Share ...

AllerVie Health

Board Certified Allergist

Towson, MD · On-site

Board Certified Allergist, Greater Baltimore, MD- Part Time and Full time About AllerVie Health: At ... Participate in quality improvement initiatives, clinical research, and continuing medical education ...

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Part Time Clinical Research Monitor information

See Silver Spring, MD salary details

$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

Research Project Interviewer - Baltimore - PT

Sago

Baltimore, MD • On-site

$18/hr

Part-time

Re-posted 26 days ago

Job description

Sago, formerly Schlesinger Group, is the global research and data partner that connects human answers to business questions. Combining our legacy of impact, global reach, and innovative spirit, we enable our clients to solve business problems through extensive audience access and an adaptive range of qualitative and quantitative solutions. We help our clients understand what their customers want and demand - empowering them to make decisions with confidence. As a partner to our clients, their clients, and the industry, Sago seamlessly connects businesses to key insights.

Join our team at SAGO, where happiness thrives in the top 35%, our work culture ranks in the top 10%, and diversity shines in the top 15% compared to peers of our size. Discover more about us athttps://www.comparably.com/companies/sago

Position Summary

The Research Project Interviewer (RPI) plays a critical role in the successful execution of research studies by supporting subject recruitment, informed consent, study visits, investigational product handling, and study documentation. This role requires strong interpersonal skills, attention to detail, and strict adherence to study protocols, regulatory requirements, and ethical research standards.
This is an on-site, part-time position that pays $18 per hour. You will be expected to work 30 hours per week.

Start date: August 17th, 2026

End date: January 29th, 2027

Key Responsibilities

  • Conduct subject interviews to assess preliminary eligibility in accordance with study protocols and defined inclusion/exclusion criteria
  • Clearly explain study objectives, procedures, risks, and participant responsibilities in a professional and participantfriendly manner
  • Obtain informed consent from eligible subjects prior to initiation of any studyrelated procedures
  • Serve as a primary point of contact for enrolled subjects, responding to questions related to study participation, visits, and procedures
  • Provide ongoing support to promote subject compliance, engagement, and retention throughout the study lifecycle
  • Schedule, coordinate, and manage subject study visits in alignment with protocoldefined timelines and visit windows
  • Confirm subject availability and provide visit reminders as needed
  • Prepare visit materials and ensure all protocolrequired assessments and procedures are completed accurately and within required windows
  • Maintain accurate inventory control, accountability, and reconciliation of investigational products
  • Receive, store, dispense, and return IP in accordance with study protocols, sponsor requirements, and regulatory standards.
  • Collaborate effectively with monitors, the Clinical Project Management team, and site staff to support overall study success
  • Assist in the recruitment and scheduling of site subjects via phone screening of potential participants
FocusGroupJobs logo

About FocusGroupJobs

Sourced by ZipRecruiter

FocusGroupJobs, based in Iselin, NJ, US, is a leading company in the market research industry. Functioning via their official website focusgroup.com, the firm connects businesses with their target audience to gather valuable insights. They specializes in organizing and conducting focus group discussions, offering businesses with crucial consumer opinions to help shape products, services, or advertising strategies. Since its foundation, the company has prioritized maintaining quality services and representing the diverse interests of the consumer world.

Industry

Marketing

Company size

51 - 200 Employees

Headquarters location

Iselin, NJ, US

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