Providence
Providence
Posted 3 months ago
Full Time
Portland, Oregon
In Person
Smart Summary
Responsibilities
Coordinates and maintains diverse activities for clinical research trials related to heart and vascular research. Responsibilities include managing regulatory activities, IRB reporting, subject recruitment, and ensuring protocol adherence in compliance with GCP guidelines.
Qualifications
You have at least one year of experience in a healthcare-related field with strong knowledge of medical terminology. A Bachelor's or Associate's degree with courses in healthcare, science, or research is also required, or one year of relevant healthcare experience.
Must Have Skills for ATS
GCP
medical terminology
Job Description
Associate Clinical Research Coordinator - Full-Time, Day Schedule
We have two openings that support Providence St. Vincent's Medical Center and Providence Portland Medical Center
Providence offers a fantastic benefits package which include but is not limited to:
Free, convenient, and ample parking
TriMet annual pass (Hop Fastpass) for benefit eligible staff who work within the Portland Service Area (does NOT include Wilsonville, Newberg, Seaside, Hood River, Washington State, or Medford)
Medical Plan Assistance Program- provides free or reduced-cost coverage to caregivers and their eligible dependents who qualify based on household size and income
Tuition reimbursement/education– includes 100% tuition paid program options; up to $5,250 per year for select undergraduate and masters degrees within Guild catalog. Required books and fees are 100% covered or reimbursable for select schools in the Guild catalog up to program funding cap
Paid Time Off – Benefit eligible caregivers receive up to 25 days per year
Retirement - The Providence retirement program consists of employer match and discretionary contributions that work together with your pre-tax (and/orRoth aftertax) contributions to help you save for retirement.
Lyra Caregiver Assistance program- Up to 25 counseling or coaching sessions per eligible member per year
The Clinical Research Coordinator I will function under the supervision of the Clinical Trials Manager. Coordinates and maintains diverse activities in the conduct of clinical research trials related to heart and vascular research. This includes, but is not limited to: coordinating and maintaining regulatory activities, IRB submissions and ongoing IRB reporting responsibilities, screening and recruitment of study subjects, obtaining informed consent from subjects, assuring protocol adherence for required study procedures, timely and accurate completion of case report forms and related study documentation, coordination of study activities with Investigators, associated departments, staff and sponsor representatives, ongoing maintenance of all study materials, products and documents. All study related activities will be conducted in compliance with the Code of Federal Regulations - Good Clinical Practice (GCP) guidelines.
Providence caregivers are not simply valued – they’re invaluable. Join our team at Providence St Vincent Medical Center in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.
Required Qualifications:
Preferred Qualifications:
Why Join Providence?
Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our Mission of caring for everyone, especially the most vulnerable in our communities.
Accepting a new position at another facility that is part of the Providence family of organizations may change your current benefits. Changes in benefits, including paid time-off, happen for various reasons. These reasons can include changes of Legal Employer, FTE, Union, location, time-off plan policies, availability of health and welfare benefit plan offerings, and other various reasons.
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