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Clinical Trials Manager Jobs in Reston, VA (NOW HIRING)

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

Coordinate operational and startup activities for clinical trials, including feasibility ... Develop and implement risk management strategies, including mitigation plans and resolution of ...

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

Coordinate operational and startup activities for clinical trials, including feasibility ... Develop and implement risk management strategies, including mitigation plans and resolution of ...

Job Summary: Responsible for assisting with coordinating clinical trials with the strictest ... Crisis management and problem solving skills; ability to react calmly and effectively in emergent ...

... management and monitoring activities throughout the clinical trial lifecycle. This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and ...

Showing results 21-40

Clinical Trials Manager information

See Reston, VA salary details

$30

$65

$100

How much do clinical trials manager jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical trials manager in Reston, VA is $65.04, according to ZipRecruiter salary data. Most workers in this role earn between $52.79 and $73.27 per hour, depending on experience, location, and employer.

What does a clinical trials manager do?

A Clinical Trials Manager oversees the planning, coordination, and execution of clinical trials to ensure they are conducted safely, efficiently, and in compliance with regulatory requirements. They manage teams, budgets, timelines, and communication between stakeholders such as sponsors, investigators, and regulatory bodies. Their responsibilities also include monitoring trial progress, resolving issues, and ensuring data integrity throughout the study.

What are some common challenges faced by clinical trials managers and how can they be addressed?

Clinical Trials Managers often encounter challenges such as ensuring regulatory compliance, managing complex timelines, and coordinating communication among diverse stakeholders. Balancing the needs of sponsors, investigators, and regulatory bodies requires strong organizational skills and attention to detail. Proactively addressing these challenges involves implementing robust project management tools, maintaining clear documentation, and fostering open communication within the team. Building relationships with site staff and regularly updating all parties can help anticipate issues early and keep trials on track.

What are the key skills and qualifications needed to thrive as a clinical trials manager, and why are they important?

To thrive as a Clinical Trials Manager, you need expertise in clinical research processes, regulatory compliance, and project management, often supported by a degree in life sciences and experience in clinical trial coordination. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring protocol adherence. These skills and qualities are crucial for maintaining trial integrity, regulatory compliance, and successful project outcomes.

What is the difference between Clinical Trials Manager vs Clinical Research Coordinator?

AspectClinical Trials ManagerClinical Research Coordinator
ResponsibilitiesOversees entire clinical trial process, manages teams, ensures compliance, and handles budgets.Assists with patient recruitment, data collection, and site coordination under supervision.
Required CredentialsBachelor’s or higher in life sciences, often with project management experience.Typically holds a bachelor’s degree in health sciences or related field; certification may be preferred.
Work EnvironmentWorks in clinical trial sites, research organizations, or pharmaceutical companies.Primarily works at clinical sites, hospitals, or research facilities.

In summary, Clinical Trials Managers oversee the entire trial process and manage teams, while Clinical Research Coordinators support daily trial activities at the site level. Both roles require relevant education and work in clinical research settings, but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Trials jobs in Reston, VA?

The most popular types of Clinical Trials jobs in Reston, VA are:

What are popular job titles related to Clinical Trials Manager jobs in Reston, VA?

For Clinical Trials Manager jobs in Reston, VA, the most frequently searched job titles are:

What cities near Reston, VA are hiring for Clinical Trials Manager jobs?

Cities near Reston, VA with the most Clinical Trials Manager job openings:

Infographic showing various Clinical Trials Manager job openings in Reston, VA as of August 2026, with employment types broken down into 87% Full Time, 11% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $135,282 per year, or $65 per hour.

Licensed Independent Social Worker (LICSW) Clinical Trials

ABSS SOLUTIONS INC

Washington, DC • On-site

$90K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 20 days ago


Job description

Job description


ABSS Solutions, Inc. (ASI), formed in 2007 and headquartered in Prince George's County, Upper Marlboro, MD is positioned to be a leader as a full service Medical & Behavioral Services provider with a global footprint. ASI is an 8(a) certified by the U.S. Small Business Administration as well as small business and Minority Business Enterprise certified by multiple jurisdictions. We pride ourselves on offering high quality specialized medical services personnel, customized consulting and training services, as well as IT products, services and staff to a variety of commercial and government agencies.

We are currently looking for a Licensed Clinical Social Worker to provide onsite mental health support for participants in ongoing clinical trials for life threatening illnesses with the NIH in Bethesda, MD. The candidate must possess Independent Licensure (LCSW-C, LICSW, or equivalent) in any of the 50 states.

Provides clinical social work services:

  • Performs individual and family supportive and psychoeducational counseling about the patient physical and/or psychiatric illness and effective ways to cope.
  • Independently provides various treatment modalities, including crisis intervention, individual, family or group psychotherapy, emotional and environmental support and resource planning.
  • Provides education regarding adjustment to illness and managing protocol related logistics.
  • Develops recommendations and plans to address areas of identified need and provide ongoing care to help participants and families access needed services.
  • Identifies possible resources and services for which research participants and families may be eligible.
  • Discusses resource options with research participants and families and refers as appropriate, based on agreement and understanding by the participant and family.
  • Explains eligibility criteria and discusses needs, educates resource participants about agency and community resources and services for which they are eligible.
  • Develops and implements treatment plans based on assessments.
  • Provides short term counseling related to adjustment to illness and protocol participation.
  • Addresses and follows up on problems requiring clinical social work services, including behavioral health needs and/or coping difficulties impacting the ability to access services.
  • Provides clinical support to patients and families throughout the time they are participating in research protocols.
  • Makes recommendations for and implements appropriate discharge plans, including psychotherapy, community services involvement, special education and activity programs
  • Documents all patient contacts and interventions in accordance with Social Work Department Policies and Procedures.
  • Complies with agency and departmental standards for documentation of patient work and data collection for performance improvement and workload tracking.
  • Conducts interviews with patients and their families and caregivers.
  • Gathers selected information through in-person and phone-based interviews, medical record review and consultation with interdisciplinary team members.

Coordinates care with medical, nursing, teaching and occupational staff as part of an interdisciplinary team:

  • Coordinates patient and family care with clinical center staff.
  • Participates in research group meetings and makes recommendations in the decision-making process regarding inclusion in studies and diagnosis.
  • Attends and participates in rounds and interdisciplinary team meetings in order to enhance team understanding of the psychosocial factors impacting research participants their health care and ability to comply with protocol participation.
  • Attends and participates in team and department meetings.

Education & Experience Requirements:

  • Must possess a Master's Degree in Social Work
  • Must be a U.S. Licensed Clinical Social worker (LCSW-C, LICSW, or equivalent)
  • A minimum of 2 years' experience working with medical patients with cancer and/or other life-limiting diagnoses.
  • Interested in being part of a team supporting clinical trial participants
  • Individual and group counseling

Job Type: Full-time

Pay: From $90,000.00 per year

Benefits:

  • 401(k)
  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance

Medical Specialty:

  • Psychiatry


Schedule:

  • 8 hour shift
  • Day shift
  • Monday to Friday


Experience:

  • Hospital Based Social Work: 2 years (Required)


License/Certification:

  • Independent Clinical Social Worker License (Required)


Work Location: Bethesda, MD 20892

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