Top 7 Senior clinical research coordinator Jobs in Oregon

Senior Clinical Research Coordinator
Headlands Research —Portland, OR
- Full-time
- Customer service
- Mid-level
- Clinic
- Health savings account
- Paid holidays
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Experienced Clinical Research Associate (CRA II / SR CRA) - US West- Multiple Therapeutic Areas Available
Thermo Fisher Scientific —Oregon
- $80,000 - $125,000 a year
- Full-time
- Background check
- Nursing
- RN License
- Commuter assistance
- Paid parental leave
6d
TI Sr Clinical Research Assistant (Clinical Research Coordinator)
Oregon Health & Science University —Portland, OR
- $50,815 - $84,697 a year
- Temporary
- Microsoft Access
- Vital signs
- Mid-level
4d
Community Research Liaison, Sr / Pathways Program Coordinator
Oregon Health & Science University —Portland, OR
- $48,214 - $68,682 a year
- Full-time
- Microsoft Word
- Customer service
- Mid-level
- Health insurance
6d
Sr. TI Clinical Research Assistant
Oregon Health & Science University —Portland, OR
- $50,814 - $84,698 a year
- Full-time
- Mid-level
- Office
- Travel
9d

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Experienced Clinical Research Associate (CRA II / SR CRA) - US West- Multiple Therapeutic Areas Available
Thermo Fisher Scientific —Oregon
Bachelor's degree in a life science related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
$80,000 - $125,000 a year
6d
Clinical Research Budgeting Analyst - Clinical Trials
Providence —Portland, OR
Will complete full evaluation and integration of internal cost during the set-up of a new clinical study; will revise study budgets following revision of study…
$37.84 - $58.75 an hour
12d

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Three years’ experience in clinical research or healthcare related field, required. CCRC or CCRP certification within 12 months of hire and maintained…

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Senior Clinical Research Coordinator

Headlands Research -
Portland, OR

Quick Apply

Job Details

Full-time

Benefits

Health savings account
Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Paid time off
Vision insurance
401(k) matching
Life insurance

Qualifications

Care documentation
Research project coordination
ICH guidelines
IVR
Clinical quality assurance standards
Clinical documentation standards
Clinical trial support in drug product development
Pharmaceutical research experience
Medical terminology
FDA regulations

Full 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.

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 for our clinical research site located in Portland, OR.

Type: Regular Full-time Employee
Schedule: M-Th: 7:30 AM - 5:30 PM
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:

Provide the highest level of care for study patients
Deliver excellent customer service to pharmaceutical clients
Coordinate all aspects of assigned clinical trials from site initiation through close-out
Conduct subject visits and ensure accurate, timely documentation in compliance with protocol and standards
Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs
Manage subject recruitment, informed consent, and retention activities
Ensure timely EDC data entry and resolution of queries
Report and follow up on AEs, SAEs, and protocol deviations
Collaborate with investigators, sponsors/CROs, labs, and internal teams
Prepare for and participate in monitoring visits, audits, and inspections
Maintain regulatory documentation and ensure training compliance for amendments and systems
Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)
Attend investigator meetings and provide cross-functional support as needed
Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory

Requirements:

At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial studies as the primary coordinator required
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 required.
Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations
Experience with EDC, IVRS, and clinical research platforms
Proficiency in medical terminology and clinical documentation
Strong organizational skills with the ability to manage multiple studies
Clear, professional verbal and written communication skills
Comfortable working onsite in a collaborative, clinical environment

Who Thrives in This Role

CRCs who want structure, support, and accountability
Those interested in taking the next step in managing people
Professionals who value teamwork over silos
Coordinators who care about data quality, patient experience, and compliance
Those ready to grow within a stable, well-established research site

Apply today if you're looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.

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 [email protected] 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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senior clinical research coordinator jobs in oregon

Senior Clinical Research Coordinator

Experienced Clinical Research Associate (CRA II / SR CRA) - US West- Multiple Therapeutic Areas Available

TI Sr Clinical Research Assistant (Clinical Research Coordinator)

Community Research Liaison, Sr / Pathways Program Coordinator

Sr. TI Clinical Research Assistant

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