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Weekend Clinical Research Jobs in Silver Spring, MD

ObjectiveHealth

Clinical Research Coordinator I

Laurel, MD · On-site

$24 - $32/hr

Description Clinical Research Coordinator I Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate ...

PRISM Vision Group

Clinical Research Coordin

Fairfax, VA · On-site

$49K - $70K/yr

NJ Eye LLC Clinical Research Coordinator NJ Eye LLC is a private equity backed, independent, integrated eye care organization with its corporate headquarters in Union, New Jersey. The company has ...

Pharmaron

Clinical Research Nurse Coordinator

Baltimore, MD · On-site

$68K - $85K/yr

Clinical Research Nurse Coordinator FLSA Status: Exempt Salary Range: $100.000 - $113.000 / yr Location: Baltimore, MD About Pharmaron Pharmaron is a global CRO (Contract Research Organization ...

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Weekend Clinical Research information

See Silver Spring, MD salary details

$50.7K

$111K

$195.4K

How much do weekend clinical research jobs pay per year?

As of Aug 9, 2026, the average yearly pay for weekend clinical research in Silver Spring, MD is $110,962.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,700.00 and $126,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in weekend clinical research?

To thrive in Weekend Clinical Research, you need a background in life sciences or healthcare, experience in clinical trial processes, and attention to detail. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and proficiency in using Microsoft Office Suite are often required. Strong organizational skills, effective communication, and the ability to work independently during off-hours are key soft skills. These capabilities are crucial to ensure accurate data collection, adherence to regulatory standards, and smooth collaboration with research teams outside standard work hours.

What is a weekend clinical research?

A Weekend Clinical Research job involves conducting or supporting clinical trials on weekends, typically for medical or pharmaceutical research. Responsibilities may include patient recruitment, data collection, monitoring study protocols, and ensuring regulatory compliance. These roles are ideal for professionals looking for flexible work schedules while contributing to medical advancements. Weekend clinical research positions are often available at hospitals, research institutions, or pharmaceutical companies.

What does a typical weekend schedule look like for weekend clinical research?

Weekend Clinical Research roles often involve supporting ongoing clinical trials by assisting with patient visits, data entry, and documentation tasks that must be completed outside of regular business hours. You may work independently or as part of a small team, coordinating closely with principal investigators and other study staff to ensure continuity and compliance with study protocols. Flexibility and reliability are important, as your work ensures that weekend operations integrate seamlessly with weekday research activities. This role is ideal for candidates looking for part-time opportunities or those balancing other weekday commitments with their passion for clinical research.

What are the most commonly searched types of Clinical Research jobs in Silver Spring, MD? The most popular types of Clinical Research jobs in Silver Spring, MD are:
What are popular job titles related to Weekend Clinical Research jobs in Silver Spring, MD? For Weekend Clinical Research jobs in Silver Spring, MD, the most frequently searched job titles are:
What job categories do people searching Weekend Clinical Research jobs in Silver Spring, MD look for? The top searched job categories for Weekend Clinical Research jobs in Silver Spring, MD are:
What cities near Silver Spring, MD are hiring for Weekend Clinical Research jobs? Cities near Silver Spring, MD with the most Weekend Clinical Research job openings:
Weekend Clinical Research jobs near you
Infographic showing various Weekend Clinical Research job openings in Silver Spring, MD as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $110,962 per year, or $53.3 per hour.

Clinical Research Coordinator

The Geneva Foundation

Bethesda, MD

$60K - $70K/yr

Full-time

Re-posted 15 days ago

Job description

About the Position
The Research Coordinator I oversees and administers research study and associated activities. Assists in project planning, and ensures that pre-established work scope, study protocol and regulatory requirements are followed. May recruit and coordinate research subjects, as appropriate, and serves as principle administration liaison for the project. Oversees and coordinates the provision of administrative and staff services to investigators; develops and maintains record keeping systems and procedures.
About the Project
This position will support multiple research projects under the MIRROR program. Musculoskeletal Injury Rehabilitation Research for Operational Readiness (MIRROR) delivers high value research, education, training, and infrastructure for over 40 clinically relevant musculoskeletal injury (MSI) studies within the military health system (MHS). MIRROR supports a broad scope of projects, including epidemiological investigation, investigator initiated pilots, and prospective randomized multisite clinical trials. Areas of clinical evaluation comprise general MSI care process models and highly prevalent anatomically-specific (e.g. back, knee, shoulder pain, etc.) targeted interventions with protocols examining effective return-to-duty activities. These studies particularly focus on deployment-limiting MSIs, ensuring that research addresses the challenges faced by service members in maintaining operational readiness. Results of these studies generate evidence-based approaches for future clinical practice guidelines as well as educational opportunities for future military and civilian providers at WRNMMC and USU.
Compensation: $60,000 - $70,000

QUALIFICATIONS

  • Bachelors degree or equivalent work experience required
  • 2-4 years experience in clinical research preferred
  • 2-4 years non-profit, research, or healthcare experience desired
  • Demonstrate competence in oral and written communication
  • Must be organized, attentive to detail, and posses a positive, friendly and professionaldemeanor
  • Must be flexible with changing priorities and able to communicate in a diplomatic andprofessional manner
  • Computer skills including at least intermediate level experience with Excel and otherMicrosoft Office Software
  • Knowledge of CFR, GCP and ICH guidelines

RESPONSIBILITIES

  • Promote safety and confidentiality of research participants at all times
  • Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices(GCP), Good Laboratory Practices (GLP), and infection control procedures
  • Plan and coordinate the initiation of research study protocol, and the implementation ofoperating policies and procedures
  • Plan, implement and maintain data collection and analysis systems in support of researchprotocol; may coordinate the collection and analysis of research data
  • Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate tospecific study objectives and work scope
  • Coordinate the day-to-day activities of technical support staff specifically engaged in thecarrying out of research/clinical protocol, as appropriate to the position; may performaspects of research protocol, as required, in accordance with specified program objectives
  • Organize and facilitate meetings, conferences, and other events associated with researchactivities; may perform and/or coordinate outreach activities, as appropriate to researchobjectives
  • Document all correspondence and communication pertinent to the research
  • Interact and communicate effectively with Principal Investigator, other site personnel,research participants, The Geneva Foundation, and the funding organization
  • Comply with all the rules and regulations as applicable to assigned duty station
  • Create and adhere to a data quality and quality assurance plan
  • Assist with interim and annual reports. S/he will be the primary liaison at the data collectionsite and will be responsible for explaining the project to military personnel associated withthe study
  • Demonstrate proficiency in performing basic study related procedures
  • Complete required and applicable research training needed to complete research
  • Maintain and update files of all applicable regulatory documentation for IACUC or IRB(including protocols, approvals, amendments, modifications, etc.) as well as anycommunications with the sponsor or any other Federal or regulatory office (including priorapprovals, change in scope, etc.)

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