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Clinical Data Associate Jobs in Gresham, OR (NOW HIRING)

Icon plc

Clinical Sample Processor I

Portland, OR

... associate services for clinical trials. About the Clinical Sample Processor role within ICON: The ... data in ICON's Lab Database, and storing samples based on protocol specifications. The Clinical ...

ICON

Clinical Sample Processor I

Portland, OR · On-site

... associate services for clinical trials. About the Clinical Sample Processor role within ICON: The ... data in ICON's Lab Database, and storing samples based on protocol specifications. The Clinical ...

Sun Life Financial

Director, Data Science

Portland, OR · On-site

We have more than 6,400 employees and associates in our partner dental practices and operate ... Explore opportunities to apply Agentic AI to augment multi-step sales, underwriting, and clinical ...

RXinsider LTD.

Clinical Associate

Portland, OR · On-site

$51 - $101/hr

As a Clinical Associate on the U.S. Abbott EP team, you will provide clinical and technical support ... Participating in clinical studies/data collection; * Troubleshooting; and, * Leading/supporting new ...

UNAVAILABLE

TI Clinical Research Associate

Portland, OR · On-site

$85 - $125/hr

This TI Clinical Research Associate will be known internally as a Float Clinical Research Associate ... Data Management * Collection and entry of oncology data from patient medical records into study ...

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All JobsClinical Data Associate JobsClinical Data Associate Jobs in Gresham, OR

Clinical Data Associate information

See Gresham, OR salary details

$14

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$91

How much do clinical data associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical data associate in Gresham, OR is $41.26, according to ZipRecruiter salary data. Most workers in this role earn between $31.06 and $41.25 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

What are the key skills and qualifications needed to thrive as a clinical data associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

What is the difference between Clinical Data Associate vs Clinical Research Coordinator?

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

More about Clinical Data Associate jobs

What are the most commonly searched types of Clinical Data jobs in Gresham, OR?

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Cities near Gresham, OR with the most Clinical Data Associate job openings:

Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Gresham, OR as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $85,831 per year, or $41.3 per hour.

Clinical Sample Processor I

Icon plc

Portland, OR

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago

Job description

Clinical Sample Processor I - Portland Oregon (OR)

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.


If you have experience handling biological lab specimens and prepping samples for delivery to a laboratory; learn how you can play a key role as an Clinical Sample Processor for ICON Laboratory Services (ILS) which is dedicated exclusively to central laboratory testing and the associate services for clinical trials.

About the Clinical Sample Processor role within ICON:

The Clinical Sample Processor will be responsible for receiving daily shipments of samples and other materials, assessing the samples upon receipt, entering data in ICON's Lab Database, and storing samples based on protocol specifications.

The Clinical Sample Processor will perform a quality check of controlled forms, scan paperwork, archive visits and other regulated documentation. Will perform barcode labeling and validation of specimens and transport specimens to the technicians in the laboratory to be analyzed.

Benefits of working at ICON:

We will provide our Clinical Sample Processors with the resources to be successful in supporting their line of business. In addition, we offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and an annual incentive plan to reward performance.

To succeed you will need:

You will possess a High School Diploma along with a preferred year of relevant accessing or clinical research industry experience, basic working knowledge of computers and accuracy and attentiveness to detail necessary and ability to lift up to 25lbs.

We invite you to review our opportunities atwww.iconplc.com/careers.

What's Next?

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment


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.

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

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