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Weekend Clinical Research Jobs in Silver Spring, MD

DelRicht Research

Clinical Research Coordinator

Vienna, VA

$24.25 - $32.25/hr

Who We Are DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new ...

Axle

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Axle is seeking a Clinical Research Coordinator to join our vibrant team at the National Institutes of Health (NIH) supporting the National Cancer Institute (NCI) located in Bethesda, MD. Benefits We ...

Axle

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Axle is seeking a Clinical Research Coordinator to join our vibrant team at the National Institutes of Health (NIH) supporting the National Cancer Institute (NCI) located in Bethesda, MD. Benefits We ...

Axle

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Axle is seeking a Clinical Research Coordinator to join our vibrant team at the National Institutes of Health (NIH) supporting the National Cancer Institute (NCI) located in Bethesda, MD. Benefits We ...

Axle

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Axle is seeking a Clinical Research Coordinator to join our vibrant team at the National Institutes of Health (NIH) supporting the National Cancer Institute (NCI) located in Bethesda, MD. Benefits We ...

Axle

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Axle is seeking a Clinical Research Coordinator to join our vibrant team at the National Institutes of Health (NIH) supporting the National Cancer Institute (NCI) located in Bethesda, MD. Benefits We ...

Axle

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Axle is seeking a Clinical Research Coordinator to join our vibrant team at the National Institutes of Health (NIH) supporting the National Cancer Institute (NCI) located in Bethesda, MD. Benefits We ...

Guidehouse

Clinical Research Coordinator

Bethesda, MD · On-site

$65K - $108K/yr

We are seeking a Clinical Research Coordinator to provide comprehensive clinical research coordination services for oncology and cancer-related clinical trials conducted within the National Cancer ...

Guidehouse

Clinical Research Coordinator

Bethesda, MD

$65K - $108K/yr

We are seeking a Clinical Research Coordinator to provide comprehensive clinical research coordination services for oncology and cancer-related clinical trials conducted within the National Cancer ...

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All JobsClinical Research JobsWeekend Clinical Research JobsWeekend Clinical Research Jobs in Silver Spring, MD

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 Site Director

DM Clinical Research

Baltimore, MD • On-site

Full-time

Re-posted 26 days ago

Job description

Clinical Research Site Director
DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an experienced Clinical Research Site Director to join our team of professionals. This role will be responsible for managing clinical trials from startup to closeout by coordinating site operations.
Responsibilities and Duties:
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents and assigned study protocol(s).
  • Responsible for immediate supervision and performance of the assigned site staff.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include, but is not limited to:
    • Sponsor provided and IRB approved Protocol Training
    • All relevant Protocol Amendments Training
    • Any study specific Manuals Training as applicable
    • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
It is the responsibility of the Site Director to make sure all the relevant training is completed prior to performing any applicable tasks on the assigned study.
  • Working knowledge of the recruitment and relevant cross functional departmental processes for their assigned protocol(s) at their respective site(s).
  • Ensuring visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s) and appropriate as well as timely follow up on the action items, at their respective sites.
  • Making sure that the most recent versions of the Protocol, Informed Consents, Study Manuals and all the other relevant study related documents are utilized and implemented at all times for the assigned protocol(s) at their respective site(s).
  • Working with the Regulatory Team to ensure maintenance of Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their as for their assigned protocol(s) at their respective site(s)
  • Working with the cross functional team(s) and site team(s) to ensure study start readiness on all the aspects and adequate training completed by all the relevant site staff prior to FPFV.
  • Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA Regulations, and ALCOA-C standards, organizational SOPs and guidance documents.
  • Responsible for providing guidance to the site team on planning and monitoring the conduct of the clinical trials.
  • Accomplishing site objectives by managing staff; facilitating staff training as applicable; communicating job expectations
  • Coaching, counseling and disciplining the employees as applicable.
  • Collaborating with both internal and external cross-functional stakeholders for the successful conduct and management of assigned protocol(s) at their respective sites.
  • To develop, coordinate, and enforce site specific systems, policies, procedures, and productivity standards.
  • Communicating and effective implementation of strategic goals from senior management
  • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
  • Striving to ensure weekly, monthly and quarterly assigned goals are met for their respective site(s).
  • Being prepared for and available at all required company meetings.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings.
  • Any other matters as assigned by management.
Experience and Skill Requirements:
  • Minimum of 8-year experience in Clinical Research.
  • 5 years Experience Managing Multiple Clinical Trials
  • Experience Managing Teams

Apply