Associate Clinical Research Coordinator

Providence • Portland, OR

1d • Onsite

About The Position

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.

Requirements

• Bachelor's Degree With courses related to healthcare, science or research. Or 1 year healthcare related experience
• Associate's Degree With courses related to healthcare, science or research. Or 1 year healthcare related experience
• Upon request: Driving may be necessary as part of this role. Caregivers are required to comply with all state laws and requirements for driving. Caregivers will be expected to provide proof of driver license and auto insurance upon request. See policy for additional information.
• 1 year Experience in healthcare related field with strong knowledge of medical terminology.

Nice To Haves

• Experience with clinical research.

Responsibilities

• 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

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree