Clinic Research Coordinator II
Listed on 2026-10-10
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Healthcare
Cardiology
Multi Care’s Pulse Heart Institute is a physician led institute with multi-specialty partnership with Cardiothoracic surgery, vascular and cardiovascular service lines. Our team and state-of-the-art programs create a world-class health care organization and the destination center for cardiac, thoracic, and vascular care with complex structural heart disease and interventions, advanced heart failure service as well as advanced imaging with cutting edge technologies.
AboutPulse Heart Institute
Multi Care’s Pulse Heart Institute is a physician led institute with multi-specialty partnership with Cardiothoracic surgery, vascular and cardiovascular service lines. Our team and state-of-the-art programs create a world-class health care organization and the destination center for cardiac, thoracic, and vascular care with complex structural heart disease and interventions, advanced heart failure service as well as advanced imaging with cutting edge technologies.
EmploymentDetails
FTE: 1.0,
Shift: Day,
Schedule:
8:00am-4:30pm
Please Note:
Phlebotomy experience heavily preferred
This position requires travel between Tacoma and Auburn locations with Auburn being the primary work site.
This position is not sponsorship eligible nor in the future.
This position does not offer relocation expenses or Interview travel expenses
Position SummaryThe Clinical Research Coordinator II independently develops and implements research project procedures that meet research objectives and ensure compliance with all aspects of Institution, Federal Drug Administration (FDA) and sponsor regulations pertaining to clinical research in human subjects (e.g. investigator financial disclosure requirements of the FDA).
Responsibilities- Develops and continually assesses priorities to ensure that projects are executed successfully and completed within required time frames to meet research objective.
- Follows guidelines for identifying subject populations, complete forms, questionnaires, and clinic procedures for collecting and summarizing observations and data.
- Retrieves medication under the direction of a licensed health care practitioner; maintain and monitor drug accountability records.
- Prepares for and participate in study monitor visits.
- Documents study visits and procedures in timely way for accurate recordkeeping to include financial accrual, source document and eCRF completion, etc.
- Identify and report all unanticipated and other adverse/serious adverse events, as well as protocol deviations, violations or exceptions.
- Modifies procedures for collecting and summarizing data.
- Bachelors’ degree preferred in science, healthcare or other related fields.
- Minimum 3 years of clinical research experience within a healthcare setting serving as a coordinator independently managing late phase drug and device trials.
- Experience using electronic data capture software required;
Clinical Trial Management Systems (CTMS). - CPR required.
- Valid Washington State driver's license
- Exceptions may be granted for internal candidates with equivalent experience instead of the Bachelor's degree
Led by physicians and advanced practice providers who understand patient needs firsthand, ensuring decisions are grounded in clinical expertise and collaboration.
Proven excellencePulse units across Multi Care earned the 2025 Chest Pain – MI Registry™ Platinum Performance Achievement Award — the only facilities in Washington to receive this distinction.
Comprehensive cardiovascular careA fully integrated model across cardiology, cardiothoracic surgery and vascular services, supporting the full continuum of care.
People-first cultureWe invest in our teams through professional development, supportive…
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