📍 Portland, OR 🏥 Summit Research Network 🕒 Full-Time | 4x10 Schedule (Mon–Thurs, 7:00am–5:30pm)

Looking for more than just high-volume blood draws?

If you’re an experienced phlebotomist or lab technician who takes pride in precision, patient care, and doing things the right way—not just the fast way—clinical research may be the next step in your career.

At Summit Research Network, our lab professionals work in a structured, calm, and purpose-driven environment, supporting clinical trials that help advance new treatments for psychiatric, dementia, and memory-related conditions.

Why Lab Professionals Choose Clinical Research

• Predictable weekday schedule (no nights, no weekends, no emergency draws)

• More time and control during patient visits and specimen handling

• Specialized lab work beyond routine phlebotomy (processing, PK handling, shipping)

• Smaller, collaborative teams where your role is respected

• Meaningful purpose—your work directly supports future medical treatments

• Clear growth pathway into higher-paying clinical research roles

This role is ideal for lab professionals who value accuracy, organization, and consistency, and who want to grow their skills beyond traditional lab or hospital settings.

Career Growth Opportunity

Summit strongly supports internal growth. High-performing Laboratory Technicians / Phlebotomists have the opportunity to progress into a Clinical Research Coordinator (CRC) role, which offers:

• Increased responsibility

• Broader study ownership

• Higher compensation

• Long-term career growth within clinical research

If you’re curious about research and want a role that can evolve with you, this position offers a clear entry point.

Position Details

• Position Type: Full-time

• Schedule: Monday–Thursday, 7:00am–5:30pm (4x10 schedule)

• Location: Onsite in Portland, OR (no remote or hybrid)

The Role

The Laboratory Technician / Phlebotomist is a key member of the clinical research team, supporting studies through specimen collection, processing, documentation, and shipment in compliance with Good Clinical Practice (GCP), study protocols, and safety regulations.

You’ll work in a controlled clinical research environment with scheduled visits, detailed protocols, and strong operational support, allowing you to focus on quality and precision.

Who Thrives in This Role

• Lab professionals who value precision over speed

• Phlebotomists looking for predictability and balance

• Candidates curious about clinical research and career growth

• Team players who take pride in quality, compliance, and patient experience

Responsibilities:

• Laboratory and Clinical Procedures
  • Perform phlebotomy, urine collection, and sample processing (centrifuging, aliquoting, labeling).
  • Prepare lab kits for each subject based on study protocols.
  • Ship biological specimens following IATA guidelines and protocol requirements.
  • Maintain specimen logs, shipping records, temperature logs, and other documentation.
  • Conduct point-of-care tests (e.g., urine drug screens, pregnancy tests).
  • Assist with patient procedures including vital signs, ECGs, and physical/neurological exam setups.
  • Clean and sanitize lab equipment and work areas daily.
  • Perform and document equipment calibration and ensure safety compliance (OSHA, HIPAA).
• Data and Documentation
  • Accurately record lab results and maintain electronic and paper logs in systems such as CRIO or eCRFs.
  • Respond to and resolve electronic data queries.
  • Verify accuracy and completeness of data entries and study documentation.
  • Participate in quality control and assurance initiatives to ensure regulatory compliance.
• Operational Support
  • Monitor and maintain inventory of lab kits and supplies.
  • Order dry ice and other lab necessities.
  • Destroy expired kits and log per protocol.
  • Support preparation of study-specific training materials and lab manuals.
  • Collaborate with study coordinators and medical staff to meet visit protocol requirements.
  • May assist with infusion monitoring under clinician supervision.

Requirements:

• Must be certified in phlebotomy
• Must have at least one full year of experience performing phlebotomy multiple times daily (preferrably with the geriatric population)
• Previous experience in clinical research is a huge plus
• Proficient with Microsoft Office (Excel, Outlook, Word) and database systems.
• Must be comfortable with performing Research Assistant tasks when the lab is slow.
• Ability to handle potentially hazardous materials safely.
• Strong organizational, time management, and multitasking skills.
• Excellent verbal and written communication; strong interpersonal skills.
• Ability to work independently and as part of a cross-functional team.
• Customer-service mindset and high level of professionalism.