TI Clinical Research Coordinator

Quest Oracle Community; Portland (OR); Presencial; USD 49.000 - 78.000; Jornada completa

Descripción de la vacante

Oregon Health & Science University (OHSU) invites applications for a Clinical Research Coordinator II within the Cardiomyopathy research team of the Knight Cardiovascular Institute. This onsite role supports patient visits, data collection, regulatory documentation, and travel coordination to ensure study visits accord with protocol.

Responsibilities include preparing visit materials, coordinating imaging and labs, entering data into sponsor systems, and assisting with sponsor visits.

Formación

• Bachelor's in a relevant field or an equivalent combo of training and experience.
• Ability to prioritize multiple tasks with strong communication skills.
• Proficient with Windows PC applications and data entry.
• Demonstrated customer service skills in person and on the phone.

Responsabilidades

• Support patient visits and scheduling with study coordinators.
• Assist data collection and entry for sponsor data systems.
• Coordinate patient travel and prepare visit documents.
• Collaborate with departments to ensure timely imaging, vitals, and tests.
• Support sponsor visits and monitoring as needed.

Conocimientos

Multitasking

Communication

Analytical thinking

Organizational skills

Teamwork

Problem solving

Customer service

Educación

Bachelor's in relevant field

Associate's OR 2 years relevant experience

3 years relevant experience

Equivalent training and experience

Herramientas

MS Excel

Oracle

Access

Word

PowerPoint

Descripción del empleo

TI Clinical Research Coordinator

US-OR-Portland

Requisition ID: 2026-39148

Position Category: Research

Job Type: Research

Position Type: Regular Full-Time

Posting Department: Cardiology Clinical Trials Unit | Knight Cardiovascular Institute

Posting Salary Range: $48,734.40 - $77,521.60 per year with offer based on experience, education and internal equity

Posting FTE: 1.00

Posting Schedule: Monday - Friday, occasional nights/weekends

Posting Hours: 7:00am - 5:30pm

Drug Testable: Yes

LinkedIn Job Code: #LI-CC1

Department Overview

The Clinical Trials Unit supports the vision of the Division of Cardiovascular Medicine, the Knight Cardiovascular Institute (KCVI) and OHSU Health to provide Oregonians with state‑of‑the‑art facilities and outstanding staff to advance treatments for cardiovascular diseases. KCVI and OHSU Health proudly collaborate to support clinical research and bring the future of cardiovascular care to the present. Our clinic, located on the South waterfront in CHH1, supports the complex care initiative and the Healthcare mission's priorities, while the CTU provides in patient trial opportunities and procedural care on OHSU main campus as well. Our unit provides the physical infrastructure to perform pharmacological and medical device trials including trials which require infusions, genetic trials, device implants, and cutting‑edge imaging.

The Knight Cardiovascular Institute Clinical Research Assistant II (Assistant Coordinator) is responsible for various duties related to clinical trials. They will assist the study coordinators in supporting patient visits, assists in data collection and entry for the sponsor, and coordinates patient travel to ensure study subjects are able to meet their visits. This position will primarily support our Cardiomyopathy research team within the division of Cardiology, they may be reassigned secondary duties to support other sections within the Cardiovascular Medicine Clinical Trials Unit and Knight Cardiovascular Institute. This is an onsite role with limited hybrid opportunities.

Function/Duties of Position

• Always promotes the mission of the Knight Cardiovascular Institute through our Professional Standards of timely Customer Service, Reliability, Productivity, Professionalism, Accuracy, Timeliness, Integrity, and Problem‑Solving.
• Responsible for many aspects of clinical trial operations from site initiation visit to closeout and assuring appropriate conduct of protocols to meet FDA guidelines. This includes but is not limited to:
  • Works in collaboration with study coordinator to maintain and file regulatory and study documents of active trials to meet study requirements
  • Create a weekly task list of outstanding items for review to ensure data entry to EDC is captured within obligatory time frames
  • Collection and transcription of all laboratory and imaging data with guidance from the coordinator as needed.
  • Data entry of visit data into central data repositories (eCRIS, internal subject trackers, etc.)
  • Addressing all imaging and laboratory queries in sponsor ERT
  • Maintaining laboratory reporting and signature requests from the PI
• Responsible for elements of patient visits including but not limited to:
  • Work with coordinator in planning visit activities and scheduling participant appointments
  • Take point on patient scheduling
  • Coordination of patient travel
  • Prepping any necessary documents prior to the visit
  • Responsible for communicating with patients regarding scheduled appointments
  • Work with coordinator in collaborating with ancillary departments to make sure all patients receive timely ECHO's, Imaging, vitals (blood pressure, temp, respirations, height, weight) or other study related tasks as needed.
  • Independently provide follow up for subjects who are no longer receiving treatment in the form of phone calls or clinic visits.
  • Work with monitoring groups to ensure all data is captured as per protocol
• Assist the Clinical Trial Leadership, coordinators, or Principal Investigator with other research related projects and administrative/office related duties as needed
• Assist manager and coordinator as needed in supporting sponsor visits (i.e. proctoring visits, monitoring, site initiation, etc.)

Required Qualifications

• Bachelor's in relevant field OR
• Associate's AND 2 years of relevant experience OR
• 3 years of relevant experience OR
• Equivalent combination of training and experience
• Ability to prioritize multiple tasks at one time
• Must have excellent communication, analytical and organizational skills: both written and verbal.
• Ability to work independently and as part of a team while being collaborative in resolving problems.
• Must have proficient with computers running Windows and PC applications e.g. MS Excel, Oracle, Access, Word and PowerPoint).
• Must have demonstrated excellent customer service skills both on the phone and in person.
• Demonstrated ability to work with a variety of diverse individuals and personalities.
• Must possess energy and drive to coordinate multiple projects simultaneously.
• Ability to use tact and diplomacy to maintain effective working relationships
• Ability to perform the job duties with or without accommodation.

Preferred Qualifications

• Bachelor's degree with coursework in Science
• At least one year general office experience
• Knowledge of cardiology. Managing Access database or similar database.
• Microsoft office, medical terminology, analytical skills, trouble shooting skills. Ability to work independently as well as within a team environment.
• BLS

Additional Details

Location: Marquam Hill & South Waterfront Campus

Schedule: Monday Friday, 6am 6pm primary business hours with variability depending on clinical schedules with occasional evenings & weekend work to meet project deadlines/goals. As a salaried employee assistant coordinators are expected to flex their time in conjunction with OHSU policy; this may mean working more than 40 hours in a week and then less another.

Must be able to travel to all KCVI worksite locations, including potentially using the tram numerous times each day. Will work with human biological samples, including samples which may contain infectious disease. Research assistant Coordinator may be expected to travel to conferences, new study meetings. Clinical Research Assistant Coordinator is required to use Personal Protective Equipment (gloves, masks, etc.) as required to maintain a safe and healthy clinical research environment. Additional safety training may be required to work in clinical research. Position requires ability to focus in a busy cubicle environment with multiple distractions. Position requires successful completion of BLS certification.

This is a patient facing on-site roll. Limited remote work is approved on an as needed basis by Clinical Trial Administrator. All obligations to clinical schedules and security of paper PHI and clinical trials regulations must be maintained at all times this severely restricting the ability to conduct work remotely.