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Clinical Data Associate Ii Jobs (NOW HIRING)

ClearNote Health

Clinical Data Engineer II/III

San Diego, CA · On-site

$150K - $190K/yr

Position Summary TheClinicalData Engineer II/IIIownsclinical Data Operations:thedatapipelines, data ... Build andmaintainELT pipelines from clinical source systems -- and non-standard sources such as ad ...

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Clinical Data Associate Ii information

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How much do clinical data associate ii jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for clinical data associate ii in the United States is $38.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $38.94 per hour, depending on experience, location, and employer.

What does a Clinical Data Associate II do?

A Clinical Data Associate II is responsible for managing and validating clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They review clinical data for completeness, identify discrepancies, and work with other clinical team members to resolve data issues. Their role often includes using specialized databases and software, performing quality checks, and generating reports to support clinical research studies. This position typically requires experience in clinical data management and knowledge of Good Clinical Practice (GCP) guidelines.

What are the key skills and qualifications needed to thrive as a Clinical Data Associate II?

To thrive as a Clinical Data Associate II, you need a strong background in life sciences or related fields, experience in clinical data management, and a keen understanding of regulatory standards. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and often certifications like CDM or GCP are typically required. Attention to detail, problem-solving skills, and effective communication set outstanding professionals apart in this role. These skills are crucial to ensure data integrity, regulatory compliance, and successful clinical trial outcomes.

How does a Clinical Data Associate II typically collaborate with other teams during a clinical trial?

As a Clinical Data Associate II, you will work closely with clinical research coordinators, data managers, biostatisticians, and project managers to ensure the accuracy and integrity of clinical data. Collaboration often involves participating in cross-functional meetings, resolving data discrepancies, and supporting the database lock process. Effective communication and teamwork are essential, as you’ll coordinate data query resolutions and contribute to continuous process improvement with other departments. This collaborative environment provides opportunities to expand your knowledge in clinical research operations and build relationships that can support your career growth.

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Clinical Data Associate Ii jobs near you
Infographic showing various Clinical Data Associate Ii job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.

Clinical Research Associate II

Blue Bell, PA • Remote

410 ICR United States USA
See more jobs at 410 ICR United States USAexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 20 days ago

Job description

CRA II or Senior CRA-US-Remote

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 in a scientific or healthcare-related field.

  • 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

#LI-JG1 #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