Clinical Research Coordinator Sr

MultiCare Health System•Tacoma, WA

4d•$32 - $46

About The Position

The Senior Clinical Research Coordinator is responsible for a variety of activities in support of clinical research studies. In addition to serving as lead coordinator on multiple clinical trials, the Senior Clinical Research Coordinator provides training, mentorship, project leadership, and quality control oversight of Coordinators and Research Assistants in assigned areas.

Requirements

Bachelors’ degree required preferably in science, healthcare, or other related fields. Equivalent combination of education and experience may be substituted for the educational requirements
Clinical Research Coordinator professional certification required.
Minimum 4 years of experience serving as lead coordinator conducting clinical trials required; worked as primary research coordinator for at least 10 drug or device trials.
Experience in startup, recruiting, and overall implementation of research protocols and clinical trials processes required.
Experience using electronic data capture software required; Clinical Trial Management Systems (CTMS).

Responsibilities

Implement and monitor clinical trials and research projects that meet MIRI and facility/clinic objectives and ensure compliance with protocol and sponsor requirements.
Identify and report all unanticipated and other adverse/serious adverse events, as well as protocol deviations, violations or exceptions.
Maintains contact with community agencies, health care providers, and/or study sponsors (i.e., NIH, pharmaceutical, and other institutions); serve as site contact and inform sponsors of status of research.
Responsible for pursuing and recruiting new studies
Verifies and coordinates all aspects of data development, maintenance, tracking, and reporting using statistical and database management programs.
Determine effective strategies for promoting/recruiting research participants and retaining participants in long term clinical trials.
Provides thoughtful, accurate input on study feasibility review, communicating on behalf of Manager with internal and external partners.
Coordinates multidisciplinary team to carry out research protocol procedures and ensures adequate training and resources are available to team.