Clinic Research Coordinator II

MultiCare Health System•Tacoma, WA

3d•$63,232 - $91,000•Hybrid

About The Position

MultiCare’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. FTE: 1.0, Shift: Day, Schedule: 8:00am-4:30pm Please Note: Phlebotomy experience heavily preferred This position requires trave between Tacoma and Auburn locations with Auburn being the primary work site. This position is not sponsorship eligible nor or in the future. This position does not offer relocation expenses or Interview travel expenses Local candidates strongly preferred Position Summary The 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).

Requirements

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

Nice To Haves

Phlebotomy experience heavily preferred

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.