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ICON plc logo

CRA

ICON plc·Austin, Texas

$91,336 - $114,170/yrFull TimeRemote OkRemote friendly2-5 yrsPosted 5 days ago
Practice for this role

CRA · $91,336 - $114,170/yr

How this role compares

Computed from live listings

  • +26% vs. median posted salary for healthcare roles in Austin, Texas ($72,694, n=487)
$20,000 · lowesthighest · $725,850
this role: $91,336median $72,694

Shaded band: the middle 50% of 487 posted healthcare roles in Austin, Texas salarys. This role sits in the 62nd percentile.

About the role

Pay for this role is about 26% above the Austin, Texas median for similar positions.

The Clinical Research Associate will conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. They will also collaborate with site staff and investigators while performing data reviews to maintain high-quality clinical trial documentation.

Clinical Research Associate - Women's Oncology - West / Central / South Region 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 Do

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Focus is early-stage development clinical trials (non-oncology)

Key responsibilities include

  • 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: You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience

Bachelor's degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. Oncology monitoring experience required 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. Willingness to travel as required up to 50% within their region (West, Central or South)

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

$91,336.00-$114,170.00 Are you a current ICON Employee? Please click here to apply

Requirements

Candidates must hold a bachelor's degree in a scientific or healthcare-related field and possess at least 2 years of experience as a Clinical Research Associate. Additionally, oncology monitoring experience and in-depth knowledge of ICH-GCP guidelines are required.

  • bachelor degree
  • Organizational skills
  • Communication skills
  • Patient safety
  • Data review
  • Clinical research
  • Data integrity
  • Protocol compliance
  • ICH-GCP guidelines
  • Site initiation
  • Clinical trial monitoring
  • Query resolution
  • Clinical study reports
  • Oncology monitoring
  • Site qualification

Posting details

Employment type
Full Time
Work arrangement
Remote Ok
Experience
2-5 yrs
Salary
$91,336 - $114,170/yr
Locations
Austin, Texas; Chicago, Illinois; Long Beach, California; Arizona; Texas; California; Kansas; Colorado
Posted
Sep 8, 2026
Application
Employer website
ICON plc logo

Hiring organization

ICON plc

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an...

IndustryBiotechnology Research
TypePublic Company
Size10,001+ employees
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Market context

Texas CRA Roles Favor Oncology and GCP Expertise

Clinical Research Associate roles in Texas commonly emphasize scientific or healthcare degrees, prior CRA experience, oncology monitoring, and strong ICH-GCP knowledge. This combination can make candidates more competitive, particularly for positions offering salaries of $91,336–$114,170 annually and benefits such as medical, dental, vision, retirement, and professional development. Before applying, compare your oncology monitoring examples with the posting; requirements and benefits here are AI-summarized from the original description, saving research time.

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