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Sr Clinical Data Manager Jobs in Reston, VA (NOW HIRING)

GRVTY

Data Manager - Senior

Falls Church, VA · On-site

The role involves overseeing data management, ensuring compliance with requirements, and serving as the primary communication interface between the customer and the team. Responsibilities : • ...

GeneDx, Inc

Senior Clinical Scientist

Gaithersburg, MD · On-site

Senior Clinical Scientist Whole Exome Sequencing Program (WES) GeneDx, Inc Gaithersburg, MD MD/PhD ... time management and communication skills are key. Expertise in pertinent areas such as Next ...

GRVTY

Data Manager - Senior

Falls Church, VA · On-site

$160K - $190K/yr

Oversee and manage data, databases, and pipelines across the full data acquisition, curation, and preprocessing lifecycle, ensuring compliance with specified requirements and priorities * Conduct ...

GRVTY

Data Manager - Senior

Falls Church, VA

What Impact You'll Have GRVTY is seeking a motivated and experienced Data Manager to provide technical and managerial leadership over our overhead satellite imagery preprocessing operations. The ...

GRVTY

Data Manager - Senior

Falls Church, VA · On-site

$160K - $190K/yr

Oversee and manage data, databases, and pipelines across the full data acquisition, curation, and preprocessing lifecycle, ensuring compliance with specified requirements and priorities * Conduct ...

Emmes

Sr. Clinical Research Associate

Rockville, MD · Hybrid

Clinical Study Manager, Lead CRA, Project Manager, etc.) independently schedules and conducts ... As part of the site visits, independently conducts Informed Consent (ICF) review, source data ...

Emmes

Senior Clinical Research Associate

Rockville, MD · On-site +1

Clinical Study Manager, Lead CRA, Project Manager, etc.) independently schedules and conducts ... As part of the site visits, independently conducts Informed Consent (ICF) review, source data ...

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Showing results 21-40

All JobsSr Clinical Data JobsSr Clinical Data Manager JobsSr Clinical Data Manager Jobs in Reston, VA

Sr Clinical Data Manager information

See Reston, VA salary details

$82.2K

$128K

$191.9K

How much do sr clinical data manager jobs pay per year?

As of Aug 11, 2026, the average yearly pay for sr clinical data manager in Reston, VA is $128,021.00, according to ZipRecruiter salary data. Most workers in this role earn between $108,700.00 and $143,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Sr Clinical Data Manager?

To thrive as a Sr Clinical Data Manager, you need expertise in clinical data management, knowledge of regulatory requirements (such as GCP and FDA), and typically a degree in life sciences or related fields. Proficiency with data management systems like Medidata Rave, Oracle Clinical, and experience with CDISC standards or relevant certifications are commonly required. Strong project management, leadership, and communication skills help you effectively oversee teams and ensure data quality. These skills and qualifications are crucial for ensuring accurate, compliant, and timely clinical trial data that supports successful regulatory submissions.

What does a Sr Clinical Data Manager do?

A Sr Clinical Data Manager oversees the collection, management, and quality control of clinical trial data. Their responsibilities include designing data collection systems, ensuring data accuracy and integrity, managing databases, and coordinating with clinical research teams. They play a critical role in ensuring that clinical data meets regulatory standards and is ready for analysis and submission. Typically, Sr Clinical Data Managers also mentor junior staff and help develop data management protocols and best practices.

What are some typical challenges a Sr Clinical Data Manager might face when overseeing multiple clinical trials simultaneously?

A Sr Clinical Data Manager often manages several trials at once, which can lead to challenges such as coordinating data collection across diverse study sites, ensuring consistent data quality, and meeting tight regulatory deadlines. Balancing these demands requires strong organizational skills, proactive communication with cross-functional teams, and effective delegation of tasks to junior data managers. Staying updated on evolving data standards and regulatory requirements is also crucial to avoid delays or compliance issues.
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Sr Clinical Data Manager jobs near you
Infographic showing various Sr Clinical Data Manager job openings in Reston, VA as of August 2026, with employment types broken down into 85% Full Time, 10% Part Time, and 5% Contract. Highlights an 78% In-person, and 22% Remote job distribution, with an average salary of $128,021 per year, or $61.5 per hour.

Senior Clinical Research Associate

Icon plc

Washington, DC • Hybrid

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 24 days ago

Job description

Senior Clinical Research Associate - Oncology - Washington DC

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


The Sr. Clinical Research Associate (Sr. CRA) willbe responsible forperforming investigative site 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, andinspectionreadiness at the clinical investigative sites.

Responsibilities:

  • Perform site management activities to support the client's Oncology site successandmaintainacontinuous state of inspection readiness

  • Act as the primary contactandfacilitateefficientcommunications between the client's clinical trial team and the sites

  • Perform remote and on-sitemonitoring/co-monitoringvisits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials

  • May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs

  • Promptly document monitoring activitiesandsubmit/approvevisit reports

  • Manage site essential document collection and TMF reconciliation with site files

  • Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals

  • Regularly review site Key Risk Indicator (KRI)metrics,issuesandaction items to detect trends and ensure prompt resolution

  • Independentlydeterminerootcauses and develop/implement site Corrective Action and Preventive Action (CAPA) plans

  • Deliver training to ensure sitescomply withthe protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs)and regulations

  • Support sites and the client's regulatory inspections

  • Contribute to site identification; drive site feasibility and qualification progress; and support site activationactivities

  • Lead site engagement initiatives and foster relationships with key Oncology sites and networks

Qualifications

  • Bachelor's degree (scientific field preferred)

  • 5+yearsmonitoringclinicaltrials independently conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials.

  • 1+ years early development trialexperience

  • Solidtumorclinicaltrial experience is required

  • Experience utilizing Veeva systems is highly preferred

  • Demonstrated experiencedeveloping/maintainingsiterelationships and securing compliance

  • ExpertiseinGxPsandOncology monitoring techniques (including Risk-Based Monitoring) and terminology

  • Experience collaborating with sitesfrominitialengagementthrough close-out phases

  • Experience activating sites

  • Experience training site staff

  • Experience supporting sites and/or sponsors in regulatory inspections

  • Experience working within a Functional Services (or in-house) monitoring model is preferred

  • Willing to travel up to 50%


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Salary Range

$110,520.00-$138,150.00

Are you a current ICON Employee? Please click here to apply

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