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Virtual Senior Clinical Research Associate Jobs (NOW HIRING)

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Senior Clinical Research Associate

Houston, TX · Hybrid

Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or Clinical Research Associate (CRA) to join our dynamic, collaborative team. In this role, you will be a key ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

Job Advert Posting We are currently seeking a Contractor Senior Clinical Research Associate to join our diverse and dynamic team. This will be for a 6 month contract. As a Clinical Research Associate ...

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Virtual Senior Clinical Research Associate information

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$36K

$94.3K

$143.5K

How much do virtual senior clinical research associate jobs pay per year?

As of Jul 19, 2026, the average yearly pay for virtual senior clinical research associate in the United States is $94,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $128,000.00 per year, depending on experience, location, and employer.

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

AspectVirtual Senior Clinical Research AssociateVirtual Clinical Research Associate
Required CredentialsTypically requires 3+ years of experience, relevant certifications (e.g., CCRP), and advanced knowledge of clinical trialsEntry to mid-level experience, often with similar certifications but less experience required
Work EnvironmentRemote, overseeing multiple sites, managing complex trial phasesRemote or hybrid, supporting trial activities under supervision
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsSimilar employers, often as entry-level or supporting roles

The Virtual Senior Clinical Research Associate typically has more experience and handles complex trial oversight, while the Virtual Clinical Research Associate is often an entry or mid-level role supporting clinical trial activities remotely.

More about Virtual Senior Clinical Research Associate jobs
What cities are hiring for Virtual Senior Clinical Research Associate jobs? Cities with the most Virtual Senior Clinical Research Associate job openings:
What states have the most Virtual Senior Clinical Research Associate jobs? States with the most job openings for Virtual Senior Clinical Research Associate jobs include:
What job categories do people searching Virtual Senior Clinical Research Associate jobs look for? The top searched job categories for Virtual Senior Clinical Research Associate jobs are:
Virtual Senior Clinical Research Associate jobs near you
Infographic showing various Virtual Senior Clinical Research Associate job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.

Senior Clinical Research Associate

410 ICR United States USA

United, PA • Remote

Full-time

Posted 22 days ago

Job description

Senior CRA / CRA II - Home-Based (United States)

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.


We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

  • Collaborating with investigators and site staff to facilitate smooth study conduct.

  • Performing data review and resolution of queries to maintain high-quality clinical data.

  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports


Your profile

  • Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role

  • Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.

  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

  • Strong organizational and communication skills, with attention to detail.

  • Ability to work independently and collaboratively in a fast-paced environment.

  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

#LI-KC2 #LI-REMOTE


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.

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