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Part Time Weekend Clinical Research Jobs in Silver Spring, MD

Clinical Research Nurse

Baltimore, MD · On-site

$31.73 - $42.31/hr

The primary responsibilities include planning and implementing clinical research protocols, delivering direct nursing care, and providing clinical coverage including nights and weekends. Key ...

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 ...

... 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 Weekend Clinical Research information

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

As of Sep 2, 2026, the average hourly pay for part time weekend clinical research in Silver Spring, MD is $23.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.88 and $26.83 per hour, depending on experience, location, and employer.

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The most popular types of Weekend Clinical Research jobs in Silver Spring, MD are:

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

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Cities near Silver Spring, MD with the most Part Time Weekend Clinical Research job openings:

Part-time or Full-time Physician - Clinical Research

Headlands Research

Baltimore, MD

Full-time, Part-time

Re-posted 12 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.