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Part Time Clinical Research Monitor Jobs in Silver Spring, MD

DC Prep

2026 Bus Monitor - Part time

Washington, DC · On-site

$15.75 - $19.75/hr

Our research-based SEL curriculum is integrated into daily instruction, helping students leverage ... Monitor will ride the bus from the Edgewood campus to the designated stops. This is a part-time, ...

DC Prep

2026 Bus Monitor - Part time

Washington, DC

$15.75 - $19.75/hr

Our research-based SEL curriculum is integrated into daily instruction, helping students leverage ... Monitor will ride the bus from the Edgewood campus to the designated stops. This is a part-time, ...

Howard University

Research Assistant-1

Washington, DC · On-site

$20 - $25/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Part-Time Administrative Assistant will provide essential administrative and coordination ... Coordinate and schedule patient recruitment activities between the clinical and research teams.

Proud Moments

In-Home Based BCBA

Rockville, MD · On-site

$90 - $100/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... 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

$79K - $96K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... 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 ...

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Showing results 21-40

All JobsClinical Research Monitor JobsPart Time Clinical Research Monitor JobsPart Time Clinical Research Monitor Jobs in Silver Spring, MD

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 Aug 15, 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 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.

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 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.

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 Associate (Per Diem Overnight Shift)

Parexel

Baltimore, MD

$20 - $22/hr

Part-time

Medical, Life, Retirement, PTO

Re-posted 27 days ago

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

30th of 73 rated research

Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Job Title: Entry level Research Associate (per diem)

Work Location: onsite in Baltimore, MD

Parexel Early Phase Clinical Unitsupports the development of innovative new medicines which are vital for public health, improving outcomes, and saving lives. The early phase and "first in human" trials are the first step in testing these novel treatments in humans.

At Parexel Baltimore, MD unit our highly trained and skilled Research Associates are crucial to ensuring the successful completion of Phase I trials. This is a great role for anyone that aspires to be an enrollment specialist, clinical research coordinator, or eventually manager. Parexel provides a great system of support to help you grow and advance your career internally.

What you'll do after training is completed(including but not limited):

  • You will understand study protocols and be able to complete required medical procedures.

  • Recruit study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments.

  • Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs.

  • Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results.

  • Prepare/monitor study supplies and stock levels in clinic/hospital.

  • Ensure basic study participant safety is provided.

  • Assist with Monitor visits (i.e., room set up, etc.).

  • Maintain and update knowledge of Clinical Operating Guidelines and their proper application.

  • Assume appropriate role with study participants and caregivers.

  • Assure quality and accuracy of source and CRF documentation.

  • Comply with Quality Management (QM) department guidelines and perform corrections for QM, CRC and Monitor/Sponsor Representative in a timely manner.

Your Profile:

  • Proven customer service experience in a fast-paced environment

  • Background working in a medical or clinical setting

  • Comfortable with prolonged periods of standing and walking

  • B.S.+ in related life science field OR HS diploma/GED with relevant experience

  • CPT/Phlebotomy is highly preferred

Hours/Shift - please note this is not a full-time opportunity we are currently seeking per diem candidates (this role is not eligible for full time benefits)

Required Training: First 4 to 6 weeks required to work 40 hours a week for training (day shift - 6:50am to 3:20pm)

After training is completed:

  • Minimum availability requirements: two 12 hour overnight shifts weekly as well as two 12-hour weekend shifts in a 4-week month OR three 12-hour weekend shifts in a 5-week month

  • The actual number of hours scheduled and confirmed can vary between 0-40 hours a week, depending on business needs (hours are not guaranteed)

  • Shift Details: overnight start usually around 7pm

  • Bi-monthly attendance may be required for training sessions, unless there are no mandatory trainings to complete

Base Pay Range: $20.00 to $22.00 per hour eligible for shift differentials

Actual salaries may vary within the range based on several factors including, but not limited to education, training, experience, professional achievement, and location.

In addition to base salary, some roles may be eligible for participation in Parexel's annual performance-based bonus plan, annual salary review and additional total rewards incentives.

Our talent acquisition team will provide additional details on our bonus plan or incentive programs for those eligible roles. For all eligible employees, we offer market leading benefit programs including paid time off, 401k match, life insurance, health insurance, and other benefit offerings in accordance with the terms of applicable plans.

EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

What Parexel employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

PAREXEL logo

About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983

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