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Clinical Sample Processor Jobs in Oregon (NOW HIRING)

Centstone HC

Phlebotomist

Albany, OR · On-site

$30 - $33/hr

Label, handle, and process specimens according to laboratory standards * Support accurate testing for blood, body fluids, tissue, and other clinical samples * Document phlebotomy services accurately ...

IQVIA

Clinical Trial Nurse

Portland, OR · On-site

$50 - $60/hr

Collect samples and data to evaluate the safety and efficacy of new medications. * You may perform ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

Natera

Manager, Clinical Trials

OR · On-site +1

Manage study contracting, budget, forecasting, accruals and payment process for all clinical trial ... Support sample management and prospective sample testing for studies where Natera functions as a ...

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Clinical Sample Processor information

What is a clinical sample processor?

Clinical Sample Processors are laboratory professionals responsible for receiving, preparing, and handling biological specimens such as blood, urine, or tissue for diagnostic testing. They ensure that samples are correctly labeled, processed according to protocols, and delivered to the appropriate departments for analysis. Their work is crucial for maintaining sample integrity and the accuracy of laboratory results, which directly impact patient care. Clinical Sample Processors must follow strict safety and quality control procedures to prevent contamination and errors.

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

To thrive as a Clinical Sample Processor, you need a solid understanding of laboratory procedures, attention to detail, and typically a degree or certification in laboratory science or a related field. Familiarity with laboratory information management systems (LIMS), sample tracking software, and standard safety protocols is essential. Strong organizational skills, reliability, and effective communication help ensure the accuracy and efficiency of sample handling. These skills and qualities are crucial for maintaining sample integrity, ensuring compliance, and supporting accurate diagnostic results.

What are some common challenges faced by clinical sample processors, and how can they be addressed?

Clinical Sample Processors often face challenges such as managing large volumes of specimens, maintaining strict sample integrity, and adhering to tight turnaround times. To address these, it's important to stay organized, follow standardized protocols meticulously, and communicate proactively with laboratory staff and couriers. Familiarity with laboratory information systems and ongoing training on biosafety procedures also help ensure accuracy and efficiency in sample handling.

What is the difference between Clinical Sample Processor vs Laboratory Technician?

AspectClinical Sample ProcessorLaboratory Technician
CredentialsTypically requires a high school diploma or associate degree; certification may enhance prospectsUsually requires a high school diploma or associate degree; certification can be beneficial
Work EnvironmentHospitals, clinics, diagnostic labs handling patient samplesResearch labs, clinical labs, hospitals performing various tests
Industry UsagePrimarily in healthcare and diagnostic settingsBroader in healthcare, research, and industrial labs

Both roles involve working with laboratory samples, but Clinical Sample Processors focus specifically on preparing patient samples for testing in healthcare settings, while Laboratory Technicians perform a wider range of testing and analysis across various laboratory environments.

What cities in Oregon are hiring for Clinical Sample Processor jobs?

Cities in Oregon with the most Clinical Sample Processor job openings:

Infographic showing various Clinical Sample Processor job openings in Oregon as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Clinical Research Coordinator I, II, or III

Portland, OR • On-site

Headlands Research
Scientific Research and Development Services • 51 - 200 employees
Learn more about Headlands Researchexternal

$25.75 - $34.25/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago

Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.
Clinical Research Coordinator (CRC) I, II, or III
Location: Portland, OR | Site Name: Summit Research Network | Full-Time | Clinical Research
Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.
We're seeking a Clinical Research Coordinator (CRC) for our clinical research site located in Portland, OR. The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.
Type: Regular Full-time Employee
Schedule: Mondays through Fridays, 8:00am - 4:30pm or 7:00am - 3:30pm
Location: Onsite in Portland, OR (no capabilities for remote or hybrid work)
Reports to: Site Director
Benefits: Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.
What We Offer
  • Competitive pay + annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays
  • A mission-driven culture focused on advancing medicine and improving patient outcomes

Why Join Us?
You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster-while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you.
Responsibilities:
  • Coordinate all aspects of assigned clinical trials from site initiation to study close-out
  • Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards
  • Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs
  • Manage subject recruitment, informed consent, and retention strategies
  • Ensure timely data entry and resolution of EDC queries
  • Report and follow up on all adverse events, serious adverse events, and deviations
  • Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems
  • Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)
  • Attend investigator meetings and provide cross-functional support as needed
  • Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control

Requirements:
  • Bachelor's degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP
  • Previous experience as a Clinical Research Coordinator required
  • Industry-sponsored trial experience strongly preferred (vaccine study experience a plus)
  • Familiarity with electronic data capture (EDC), IVRS, and other trial platforms
  • Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures
  • Proficiency in medical terminology and clinical documentation practices
  • Strong interpersonal, verbal, and written communication skills
  • Organized, detail-oriented, and capable of managing multiple priorities
  • Proficient in Microsoft Office and other clinical research systems

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Need Assistance?
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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