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Part Time Clinical Research Contract Jobs in Silver Spring, MD

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 ...

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Part Time Clinical Research Contract information

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$42

$72

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

As of Aug 18, 2026, the average hourly pay for part time clinical research contract 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 is a part time clinical research contract?

A part-time clinical research contract is a work agreement where an individual is hired to assist with clinical research projects on a part-time basis, typically for a set duration or specific project. These contracts often involve roles such as study coordination, data collection, patient recruitment, or regulatory compliance. The part-time nature allows flexibility in hours and workload, making it ideal for students or professionals seeking supplementary experience. Contract terms, responsibilities, and compensation are usually outlined clearly before work begins. This arrangement benefits both employers needing temporary or specialized help and workers seeking flexible opportunities.

What are the typical responsibilities and challenges faced in a part time clinical research contract role?

In a part-time clinical research contract role, you may be responsible for tasks such as data collection, patient recruitment, regulatory documentation, and coordinating study visits, often within a limited number of hours each week. One common challenge is balancing multiple studies or priorities while adhering to strict compliance and reporting deadlines. You’ll frequently collaborate with research coordinators, principal investigators, and sometimes sponsors to ensure the smooth progress of clinical trials. Adapting quickly to evolving protocols and maintaining clear communication with the team are key to success in this flexible, yet demanding, position.

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

To thrive in a Part Time Clinical Research Contract role, you need a solid understanding of clinical research processes, regulatory compliance, and relevant science or healthcare education. Familiarity with tools such as clinical trial management systems (CTMS), electronic data capture (EDC), and knowledge of GCP (Good Clinical Practice) guidelines or related certifications is often required. Strong organizational skills, attention to detail, and effective communication are critical soft skills for coordinating studies and liaising with stakeholders. These competencies ensure protocol adherence, data integrity, and successful collaboration within research teams.

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

AspectPart Time Clinical Research ContractPart Time Clinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree in health sciences or related field; often holds certifications like CCRP or CRC
Work EnvironmentTemporary, project-based settings within research organizations or pharmaceutical companiesOngoing role within clinical sites or research organizations, overseeing study activities
Employer & Industry UsageUsed by research organizations, pharmaceutical companies, and CROs for specific projectsCommonly employed by hospitals, research centers, and clinical trial sites

In summary, a Part Time Clinical Research Contract is a temporary, project-specific role often filled by professionals with relevant certifications, while a Part Time Clinical Research Coordinator is a more ongoing position responsible for managing daily study activities at clinical sites. Both roles require similar credentials but differ in scope and employment type.

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 Contract jobs in Silver Spring, MD?

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

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

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

Part Time Clinical Research Contract jobs near you

Part-time or Full-time Physician - Clinical Research

Headlands Research

Baltimore, MD • On-site

Full-time, Part-time

Re-posted 28 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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