1

Clinical Research Study Manager Jobs in Reston, VA

Clinical Study Manager, Lead CRA, Project Manager, etc.) independently schedules and conducts ... Expertise in clinical research operations, including interpretation and implementation of country ...

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Support maintenance of databases, tracking systems, and study metrics * Ensure compliance with data management plans and quality standards * Coordinate multiple clinical research studies ...

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Support maintenance of databases, tracking systems, and study metrics * Ensure compliance with data management plans and quality standards * Coordinate multiple clinical research studies ...

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Support maintenance of databases, tracking systems, and study metrics * Ensure compliance with data management plans and quality standards * Coordinate multiple clinical research studies ...

next page

Showing results 1-20

Clinical Research Study Manager information

See Reston, VA salary details

$51K

$111.7K

$196.6K

How much do clinical research study manager jobs pay per year?

As of Jul 27, 2026, the average yearly pay for clinical research study manager in Reston, VA is $111,668.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,300.00 and $127,400.00 per year, depending on experience, location, and employer.

What does a Clinical Research Study Manager do?

A Clinical Research Study Manager oversees the planning, execution, and completion of clinical trials to ensure they are conducted ethically and in compliance with regulatory standards. They coordinate with research teams, manage budgets and timelines, and ensure accurate data collection and reporting. Their role is crucial in ensuring that clinical studies run smoothly and produce reliable results that can be used for regulatory submissions or scientific publications.

What are the key skills and qualifications needed to thrive as a Clinical Research Study Manager, and why are they important?

To thrive as a Clinical Research Study Manager, you need expertise in clinical trial management, regulatory compliance, and protocol development, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as GCP (Good Clinical Practice) are typically required. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure smooth study execution. These skills and qualifications are crucial for maintaining study integrity, meeting regulatory standards, and delivering successful clinical trial outcomes.

What are some common challenges faced by Clinical Research Study Managers in coordinating multi-site studies?

Clinical Research Study Managers often encounter challenges in ensuring consistent protocol adherence and data integrity across multiple study sites. Coordinating communication between site teams, managing timelines, and troubleshooting unexpected issues such as recruitment delays or regulatory hurdles are frequent tasks. Successful managers use strong organizational skills and proactive planning to mitigate these challenges, and often rely on regular meetings and digital tools to keep all stakeholders aligned. Establishing clear processes and fostering open communication are key to overcoming these complexities and ensuring study success.

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

AspectClinical Research Study ManagerClinical Research Coordinator
CredentialsBachelor's degree, often with experience in project managementBachelor's degree in health sciences or related field, certification optional
Work EnvironmentOversees multiple studies, manages teams, and coordinates with sponsorsHandles daily study activities, patient interactions, and data collection
Employer & IndustryPharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentUnderstanding managerial roles, responsibilities, and qualificationsFocus on operational tasks and patient management

The Clinical Research Study Manager typically oversees multiple studies, manages teams, and liaises with sponsors, requiring project management skills. In contrast, the Clinical Research Coordinator handles daily study activities, patient interactions, and data collection at research sites. Both roles are essential in clinical research but differ in scope and responsibilities.

What are popular job titles related to Clinical Research Study Manager jobs in Reston, VA? For Clinical Research Study Manager jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Clinical Research Study Manager jobs in Reston, VA look for? The top searched job categories for Clinical Research Study Manager jobs in Reston, VA are:
What cities near Reston, VA are hiring for Clinical Research Study Manager jobs? Cities near Reston, VA with the most Clinical Research Study Manager job openings:
Clinical Research Coordinator 1 - Oncology

Clinical Research Coordinator 1 - Oncology

Inova Primary Care

Fairfax, VA • On-site

$24.75 - $33/hr

Full-time

Medical, Dental, Vision, PTO

Posted 8 days ago


Inova Health System rating

7.5

Company rating: 7.5 out of 10

Based on 251 frontline employees who took The Breakroom Quiz

230th of 890 rated healthcare providers


Job description

Inova Schar Cancer Research is looking for a dedicated Clinical Research Coordinator 1 - Oncology to join the Team. This full-time role will be day-shift working Monday - Friday located in Fairfax, VA. 

The Clinical Research Coordinator 1 - Oncology implements research studies and ensures research and human subject protection within Inova from site selection to study closure. Coordinates financial aspects of study implementation and management from protocol feasibility through study closure. Develops a basic level of understanding of study coordination and the ability to perform a variety of tasks under direct supervision. Participates in several different types of clinical studies (investigational products, study phases, therapeutic areas and indications).

Inova is consistently ranked a national healthcare leader in safety, quality and patient experience. We are also proud to be consistently recognized as a top employer in both the D.C. metro area and the nation.

Featured Benefits:

  • Committed to Team Member Health: offering medical, dental and vision coverage, and a robust team member wellness program. 
  • Retirement:Inova matches the first 5% of eligible contributions - starting on your first day. 
  • Tuition and Student Loan Assistance: offering up to $5,250 per year in education assistance and up to $10,000 for student loans. 
  • Mental Health Support:offering all Inova team members, their spouses/partners, and their children 25 mental health coaching or therapy sessions, per person, per year, at no cost. 
  • Work/Life Balance:offering paid time off, paid parental leave, flexible work schedules. 

Clinical Research Coordinator 1 - Oncology Responsibilities:

  • Identifies and explains key protocol elements and performs study tasks under direct supervision.
  • Explains basic elements of subject safety including the reasoning behind the required use of an Institutional Review Board/Independent Ethics Committee, study activity documentation, and event reporting requirements.
  • Demonstrates subject protection under direct supervision.
  • Explains the investigational products development process and identify key regulations to control these processes.
  • Explains and performs study operational activities in compliance with Good Clinical Practice (GCP), and non-GCP related study management activities.
  • Explains how to document data according to ALCOA-C (Attributable, Legible, Contemporaneous, Original, Accurate and Complete) principles.
  • Explains the importance of professional conduct and describe leadership principles that impact the effective operation of an investigative site.
  • Explains the variety of communication channels, roles and relationship and outlets for study results that impact the conduct of clinical research.
  • May perform other duties as assigned.

Minimum Qualifications:

  • Education: Associate's Degree or relevant experience in lieu of a degree
  • Experience: 2 years of patient care experience or 1 year of clinical research experience with a Bachelor's Degree

Preferred Qualifications:

  • Certified Clinical Research Coordinator preferred.

  • Experience leading informed consent discussions and enrolling participants in clinical research studies preferred.

  • Experience developing, implementing, and/or evaluating clinical research protocols and operational workflows preferred.

  • Experience screening patients for research study eligibility and collaborating effectively within multidisciplinary teams, including physicians, healthcare providers, research coordinators, and other research staff preferred.

  • Experience collecting, managing, and verifying research data for accuracy against source documentation preferred.

We are Inova, Northern Virginia's leading nonprofit healthcare provider. Every day, our 26,000+ team members provide world-class healthcare to the communities we serve. Our people are the reason we're a national leader in healthcare safety, quality and patient experience. And from best-in-class facilities to professional development opportunities, we support them at every step. At Inova, we're constantly striving to be ever better - to shape a more compassionate future for healthcare. 

Inova Health is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, disability, gender identity or expression, marital status, national or ethnic origin, political affiliation, pregnancy (including childbirth, pregnancy-related conditions and lactation), race, religion, sex, sexual orientation, veteran status, genetic information, or any other characteristics protected by law.


What Inova Health System employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom