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Weekend Clinical Research Jobs in Silver Spring, MD

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Concentric Methods is seeking an experienced Clinical Research Coordinator to independently provide support services to the NIH. The total hourly pay for this non-exempt position is $30.00 for up to ...

Looking for a Clinical Research Coordinator or a Clinical Research Associate to join our team! About this role: - Hybrid 2 Days onsite & 3 Days Remote - Must have CRO experience!!!! The In-House ...

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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 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:
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

Cape Fox SS

Bethesda, MD

$26 - $34.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago


Job description

Concentric Methods is seeking an experienced Clinical Research Coordinator to independently provide support services to the NIH. The total hourly pay for this non-exempt position is $30.00 for up to 40 hours per week. This rate represents the company's good faith and reasonable estimate of possible compensation at the time of posting

In addition, for eligible positions we offer a variety of benefits including specified holidays, paid leave, health insurance, dental insurance, vision insurance, life and disability insurance, tuition reimbursement, as well as 401K with company match. This job will be posted until filled or withdrawn. Supports clinical staff develop, implement and maintain clinical research data files and materials.

- Assist preparing and submitting for review accurate source documents related to all research procedures. Collects research data and prepares information for inputs and analysis. - Work with staff on data acquisition and analysis using a variety of methods, including recruitment, entry, management and display for the Department of Bioethics research studies.

Supports the development of forms and questionnaires. - Work with staff to coordinate the logistics of courses and workshops, including the course Ethical and Regulatory Aspects of Clinical Research, and the Empirical Research Lab. Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.

- Conduct literature searches; gather and synthesize background information. Monitors subject's progress and reports adverse events. - Assist staff writing progress reports and contributions to peer-reviewed scientific manuscripts.

Supports assembly, development and review of new research projects. - Work with staff on manuscript preparation for research studies and manuscript submission. - Prepare materials for IRB submission, manuscript transmittals and other necessary approvals and reviews.

Supports the creation and management of clinical websites and web-based tools. - Collaborate with staff on the maintenance of Departmental metrics, databases and website.Preferred Professional Experience: Manuscript preparation - Data acquisition - Coordinating events - Protocol development - Statistical Analysis - Recruitment - Research Familiarity with STATA and NVivo Education and Certifications: Bachelor's Degree Required Two years of related experience Core Skills: Strong organizational and time management skills. Excellent interpersonal and communication skills

Attention to detail in data collection and documentation. Proficiency in relevant computer applications and software. Ability to work both independently and collaboratively.

Problem-solving and critical-thinking abilities.Preferred Professional Experience: Manuscript preparation - Data acquisition - Coordinating events - Protocol development - Statistical Analysis - Recruitment - Research Familiarity with STATA and NVivo Education and Certifications: Bachelor's Degree Required Two years of related experience Core Skills: Strong organizational and time management skills. Excellent interpersonal and communication skills. Attention to detail in data collection and documentation

Proficiency in relevant computer applications and software. Ability to work both independently and collaboratively. Problem-solving and critical-thinking abilities.