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Part Time Clinical Research Associate Jobs in Silver Spring, MD

ICF

On-Call Research Associate

Reston, VA · On-site

ICF Next is looking for a Research Associate to play a critical role in supporting Federal ... This is an On-Call/Part-Time role with the expectation that the successful candidate will work on ...

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

Part Time Clinical Research Associate information

See Silver Spring, MD salary details

$12

$42

$72

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

As of Jul 29, 2026, the average hourly pay for part time clinical research associate in Silver Spring, MD is $42.51, according to ZipRecruiter salary data. Most workers in this role earn between $29.81 and $54.42 per hour, depending on experience, location, and employer.

What are some common challenges faced by part-time Clinical Research Associates, and how can they be managed effectively?

Part-time Clinical Research Associates (CRAs) often face the challenge of balancing multiple study sites and projects within limited working hours. Time management and clear communication with both the research team and site staff are crucial to ensure all monitoring visits, documentation, and regulatory requirements are met on schedule. Additionally, part-time CRAs may need to be proactive in staying updated on study protocols and industry regulations, as they may not be present for all in-person team meetings. Establishing structured routines and leveraging digital tools for remote collaboration can help manage these challenges effectively.

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

AspectPart Time Clinical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often certifications like CCRP or RACBachelor's degree, often certifications like CCRP or RAC
Work EnvironmentMonitoring clinical trials at sites, remote or onsiteManaging trial operations at research sites
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinics
Search & Comparison IntentUnderstanding monitoring roles in trialsManaging trial activities at sites

Part Time Clinical Research Associates primarily focus on monitoring clinical trial progress, ensuring compliance, and verifying data accuracy, often working remotely or onsite. Clinical Research Coordinators handle the day-to-day operations at research sites, including patient recruitment and data collection. Both roles require similar credentials but differ in responsibilities and work settings.

What are the key skills and qualifications needed to thrive as a Part Time Clinical Research Associate, and why are they important?

To thrive as a Part Time Clinical Research Associate, you need a background in life sciences or healthcare, knowledge of clinical research protocols, and often a bachelor’s degree in a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certification such as ACRP or SOCRA is highly valued. Strong attention to detail, organizational skills, and effective communication are essential soft skills for monitoring trials and collaborating with research teams. These skills ensure regulatory compliance, accurate data collection, and efficient trial execution, all critical for successful clinical research outcomes.

What are part-time Clinical Research Associates?

Part-time Clinical Research Associates (CRAs) are professionals who monitor and manage clinical trials on a flexible or reduced-hour schedule, rather than full-time. They are responsible for ensuring that studies comply with regulatory requirements, collecting data, and acting as a liaison between clinical trial sites and sponsors. Part-time CRAs may work remotely or travel to research sites as needed, and their schedules can vary depending on the needs of the research project. This role is ideal for those seeking work-life balance or supplementing other professional activities. Their work is critical in advancing medical research and ensuring patient safety.
What are the most commonly searched types of Part Time Clinical Research jobs in Silver Spring, MD? The most popular types of Part Time Clinical Research jobs in Silver Spring, MD are:
What are popular job titles related to Part Time Clinical Research Associate jobs in Silver Spring, MD? For Part Time Clinical Research Associate jobs in Silver Spring, MD, the most frequently searched job titles are:
What job categories do people searching Part Time Clinical Research Associate jobs in Silver Spring, MD look for? The top searched job categories for Part Time Clinical Research Associate jobs in Silver Spring, MD are:
What cities near Silver Spring, MD are hiring for Part Time Clinical Research Associate jobs? Cities near Silver Spring, MD with the most Part Time Clinical Research Associate job openings:
Part Time Clinical Research Associate jobs near you
Infographic showing various Part Time Clinical Research Associate job openings in Silver Spring, MD as of June 2026, with employment types broken down into 47% Full Time, 49% Part Time, 1% Temporary, and 3% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $88,431 per year, or $42.5 per hour.

Part-time or Full-time Physician - Clinical Research

Headlands Research

Baltimore, MD • On-site

Full-time, Part-time

Re-posted 8 days ago

Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.
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.

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Need Assistance?
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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