Home › Companies › Headlands Research › Clinical Research Coordinator I or II
Clinical Research Coordinator I or II
Headlands Research · Portland, Oregon · Remote · Active · Greenhouse
Job facts
| Field | Value |
|---|---|
| Company | Headlands Research |
| Title | Clinical Research Coordinator I or II |
| Normalized title | - |
| Department / team | Clinical: Clinical Research Coordinators |
| Location | Portland, OR, United States |
| Work model | Remote / Remote |
| Employment type | - |
| Salary | - |
| Status | active |
| ATS provider | Greenhouse |
| Posted / first seen | 2026-04-22 / 2026-05-29 |
| Changed / last seen | 2026-06-06 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Headlands Research. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Greenhouse. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Portland. | Open |
| Department jobs | Active postings in Clinical: Clinical Research Coordinators. | Open |
| Work model jobs | Active Remote postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Headlands Research |
| Source | e23d6a19-316a-4d35-86ab-185a78ba56af |
| ATS provider | Greenhouse |
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.
📍 Portland, OR 🏥 Summit Research Network 🕒 Full-time | Onsite (no opportunities for hybrid or remote)
For experienced CRCs looking for stability, collaboration, and meaningful work
If you’re an experienced Clinical Research Coordinator who values strong operations, multidisciplinary collaboration, and a schedule that actually supports work–life balance , Summit Research Network may be the right next step in your career.
Our Portland site is known for its depth of experience, thoughtful study execution, and team-based approach to clinical research—particularly in memory studies.
About Summit Research Network
Since 1976, Summit Research Network has worked in cooperation with pharmaceutical companies to develop new medical treatments for various of conditions by conducting 500+ clinical trials. With decades of experience, Summit Research Network provides the most advanced clinical research, including our Memory Health Center, to help develop better treatments and better future health for individuals with psychiatric, dementia, age related memory issues and many other health conditions.
Why Experienced CRCs Choose Summit
Multi-disciplinary collaboration with seasoned investigators and clinical staff
Strong operational support and clear SOPs
Exposure to complex, meaningful studies—not just high-volume turnover
Backing of a growing research network with resources and stability
This role is ideal for CRCs who enjoy owning their studies , working with competent teams , and being trusted to execute with precision.
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.
Full job record
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| Source ID | e23d6a19-316a-4d35-86ab-185a78ba56af |
| Board ID | e23d6a19-316a-4d35-86ab-185a78ba56af |
| Provider | greenhouse |
| Provider Job Key | 4226823009 |
| Title | Clinical Research Coordinator I or II |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Portland, Oregon |
| Department | Clinical: Clinical Research Coordinators |
| Team | — |
| Employment Type | — |
| Workplace Type | remote |
| Remote Policy | remote |
| Country | United States |
| Region | OR |
| City | Portland |
| Salary Raw | — |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://job-boards.greenhouse.io/headlandsresearch/jobs/4226823009 |
| Apply URL | https://job-boards.greenhouse.io/headlandsresearch/jobs/4226823009 |
| First Seen At | 2026-05-29 23:03:28Z |
| Last Seen At | 2026-06-06 07:35:27Z |
| Last Checked At | 2026-06-06 07:35:27Z |
| Last Changed At | 2026-06-06 07:35:27Z |
| Inactive At | — |
| Source Posted At | 2026-04-22 13:37:43Z |
| Source Updated At | 2026-06-05 21:10:24Z |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=greenhouse/board=headlandsresearch/date=2026-06-06/2026-06-06T07-35-27-471Z-d629580194ffb9338d4a5a9fffd7c22e9f2a892d18626c9981b7afa9b7fe7951.json |
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