Clinical Research Coordinator Job at IsoTalent, Portland, OR

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  • IsoTalent
  • Portland, OR

Job Description

Job Description

Clinical Research Coordinator

Location/Onsite: Portland, OR – Onsite (Tigard area)

Our client, a leading clinical research site in the Portland metro area, is looking for a Clinical Research Coordinator to join their growing team onsite in Portland, OR. Do you have a keen eye for detail and a passion for advancing healthcare through research? Are you comfortable working directly with patients and clinical data in a fast-paced environment? Do you want to grow your skills in a supportive and mission-driven setting? If yes, this may be the perfect Clinical Research Coordinator position for you. Keep scrolling to see what this company has to offer.

The Perks!

  • Compensation: $23.00–$25.00/hour, based on experience
  • 401(k) with employer matching
  • Health insurance
  • Dental insurance
  • Paid time off
  • Flexible spending account

A Day in the Life of the Clinical Research Coordinator

As a Clinical Research Coordinator, you'll play a critical role in supporting clinical trials from start to finish. You'll work closely with investigators and research teams to ensure trial protocols are followed, data is accurately collected, and patient safety is prioritized. Your contributions help bring new treatments and medical solutions to life.

Responsibilities include:

  • Assist with the setup, coordination, and execution of clinical trials
  • Follow clinical trial protocols and ensure compliance at all stages
  • Interact directly with patients to explain studies, obtain consent, and guide them through visits
  • Collect medical histories, perform basic lab procedures, and conduct phlebotomy
  • Document data accurately in case report forms (CRFs) and resolve any data queries
  • Monitor clinical and lab data for accuracy and regulatory compliance
  • Help complete and manage required regulatory documentation
  • Maintain a professional, ethical, and compassionate approach with all study participants

Requirements and Qualifications:

  • 1+ year of experience in the healthcare industry
  • 1+ year of experience coordinating and executing clinical drug trials under the direction of site leadership and investigators
  • Ability to reliably commute to Tigard, OR
  • Experience working in a startup culture or similar - understanding that things change quickly and you may have to pivot quickly
  • Strong communication skills and attention to detail
  • Willingness to learn and grow with on-the-job training and continuing education

About the Hiring Company:

Our client is a respected clinical research site. They specialize in conducting high-quality clinical drug trials across a variety of therapeutic areas. With a strong focus on patient safety, protocol adherence, and operational excellence, they offer a collaborative environment where every team member plays a vital role in driving medical progress.

Come Join Our Clinical Research Team!

Start by filling out this 3-minute, mobile-friendly application here. We look forward to hearing from you!

Job Tags

Flexible hours,

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