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Senior Cra Jobs in Reston, VA (NOW HIRING)

ICON

Senior CRA

Washington, DC · On-site +1

Sr CRA Northern VA oncology 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 ...

410 ICR United States USA

Senior CRA

Washington, DC

Sr CRA Northern VA oncology 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 ...

New

Icon plc

Senior CRA

Washington, DC

Sr CRA Northern VA oncology 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 ...

IQVIA

CRA 2/Senior CRA 1

Rockville, MD · On-site

$90K - $175K/yr

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical ...

IQVIA

CRA 2/Senior CRA 1

Rockville, MD · On-site

$90K - $175K/yr

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical ...

ICON

Senior Clinical Research Associate

Washington, DC · On-site +1

$110K - $138K/yr

This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites. Responsibilities:

Icon plc

Senior Clinical Research Associate

Washington, DC · Hybrid

$110K - $138K/yr

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 ...

Emmes

Sr. Clinical Research Associate

Rockville, MD

Overview Sr. Clinical Research Associate Be Part of One Team, One Purpose. At Emmes Group , we're ... The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable ...

Emmes

Senior Clinical Research Associate

Rockville, MD · On-site +1

Overview Senior Clinical Research Associate US Remote Emmes Group: Building a better future for us ... The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable ...

EagleBank

Chief Compliance Officer

Bethesda, MD · Hybrid

$176K - $303K/yr

... senior management, management committees, Board committees on the following: * Compliance risks, program effectiveness, and regulatory developments * CRA performance, including lending analysis ...

EagleBank

Chief Compliance Officer

Bethesda, MD · On-site

$176K - $303K/yr

... senior management, management committees, Board committees on the following: * Compliance risks, program effectiveness, and regulatory developments * CRA performance, including lending analysis ...

EagleBank

US-MD-Bethesda

Bethesda, MD · Hybrid

$176K - $303K/yr

... senior management, management committees, Board committees on the following: * Compliance risks, program effectiveness, and regulatory developments * CRA performance, including lending analysis ...

EagleBank

Chief Compliance Officer

Bethesda, MD · On-site

$176.97 - $303.37/hr

... senior management, management committees, Board committees on the following: * Compliance risks, program effectiveness, and regulatory developments * CRA performance, including lending analysis ...

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All JobsCra JobsSenior Cra JobsSenior Cra Jobs in Reston, VA

Senior Cra information

See Reston, VA salary details

$37.5K

$98.1K

$149.3K

How much do senior cra jobs pay per year?

As of Jul 18, 2026, the average yearly pay for senior cra in Reston, VA is $98,121.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,000.00 and $133,200.00 per year, depending on experience, location, and employer.

How does a Senior Clinical Research Associate (CRA) typically collaborate with site staff and project teams during a clinical trial?

A Senior CRA regularly works with site staff, including investigators and coordinators, to ensure clinical trials are conducted according to protocol, regulatory requirements, and Good Clinical Practice (GCP) guidelines. They serve as a key liaison, communicating study updates, addressing site concerns, and providing training when needed. Additionally, Senior CRAs often collaborate with project managers, data managers, and other CRAs to monitor progress, resolve issues, and ensure data integrity. This teamwork is critical for maintaining study timelines and overall trial quality.

What is the difference between Senior Cra vs Clinical Research Associate?

AspectSenior CraClinical Research Associate
Required CredentialsBachelor's degree, experience in clinical trials, often some certificationsBachelor's degree, entry-level to mid-level experience, some certifications
Work EnvironmentLeads monitoring activities, manages sites, mentors junior staffPerforms site monitoring, data collection, and compliance checks
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms

The main difference between a Senior Cra and a Clinical Research Associate is experience level and responsibilities. Senior Cras typically oversee monitoring activities, mentor junior staff, and handle more complex tasks, while Clinical Research Associates focus on site monitoring and data collection. Both roles are essential in clinical trials and share similar industry environments and credentials.

What jobs can I get after being a CRA?

After working as a Clinical Research Associate (CRA), you can transition into roles such as Clinical Project Manager, Clinical Operations Manager, Regulatory Affairs Specialist, or Medical Writer. These positions often require experience in clinical trial management, regulatory knowledge, and strong communication skills, and may involve overseeing study progress, ensuring compliance, or coordinating between teams.

What are the key skills and qualifications needed to thrive as a Senior Clinical Research Associate (CRA), and why are they important?

To thrive as a Senior Clinical Research Associate, you need deep knowledge of clinical trial protocols, regulatory guidelines (such as GCP), and several years of hands-on experience in clinical monitoring. Familiarity with electronic data capture (EDC) systems, CTMS platforms, and certifications like ACRP or SOCRA are commonly required. Excellent organizational skills, attention to detail, and effective communication are soft skills that set top candidates apart. These skills ensure trial integrity, regulatory compliance, and smooth collaboration among sponsors, sites, and teams.

What does a senior CRA do?

A senior Clinical Research Associate (CRA) oversees and monitors clinical trials to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. They coordinate site activities, review data quality, and may mentor junior staff, often using monitoring tools and working closely with investigators and sponsors. Strong organizational skills and knowledge of clinical trial processes are essential for this role.

How much does a senior CRA make at Thermo Fisher?

A Senior Clinical Research Associate (CRA) at Thermo Fisher typically earns between $80,000 and $110,000 annually, depending on experience, location, and certifications. The role involves monitoring clinical trials, ensuring compliance, and working with clinical data management tools.

What are Senior CRAs?

Senior Clinical Research Associates (Senior CRAs) are experienced professionals responsible for overseeing and monitoring clinical trials to ensure compliance with regulatory guidelines, protocols, and good clinical practice. They play a key role in managing study sites, reviewing data, and ensuring the integrity and quality of clinical research. Senior CRAs also mentor junior staff, resolve complex issues, and maintain effective communication between sponsors, sites, and regulatory bodies. Their expertise helps ensure that clinical trials are conducted safely and efficiently.

What is the average salary of a CRA in the US?

The average salary of a Clinical Research Associate (CRA) in the US is approximately $70,000 to $90,000 per year, depending on experience, location, and certifications. Senior CRAs with extensive experience can earn over $100,000 annually, often with additional benefits and bonuses.
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Senior Cra jobs near you
Senior CRA

Senior CRA

ICON

Washington, DC • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 24 days ago

Job description

Sr CRA Northern VA oncology
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.
What You Will Be Doing:
  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:
  • Advanced degree in a relevant field such as life sciences, nursing, or medicine.
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Must be located in the MidWest (Illinois, Indiana, Iowa, Kansas, Michigan, Minnesota, Missouri, Nebraska, North Dakota, Ohio, South Dakota, and Wisconsin)
  • Oncology monitoring experience is required
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license

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 request here.
Salary Range
Are you a current ICON Employee? Please click here to apply

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