Avera
Healthcare
ClinicalResearchCoordinatororResearchAssistant
“Clinical Research Coordinator or Research Assistant at Avera. Skills: implementation of the study protocol, recruitment plan, study visits, data, study assessments, informed consent, data documentation, reporting deviations, violations, serious adverse events. implementation of the study protocol. recruitment plan”
What You'll Achieve.
improving health and wellbeing of individuals and the community
Industry & Context.
relocation to Pierre, South Dakota
What They're Looking For.
Must Have
High School Diploma or GED
Nice to Have
Bachelor's From a four year college or university within the health and science field, 1-3 years Human Research, 1-3 years Laboratory or clinical
What You'll Do.
implementation of the study protocol
collects and manages data
timely entry into the electronic data capture system
Collects and assists with processing all laboratory specimens
Maintains inventory of laboratory supplies and study kits
and enrolls study participants
Preforms the informed consent
answering all participant questions
obtaining appropriate sign-off
Ensures the adherence to ethical practices
Ensures validity of research results
and complete data documentation
and serious adverse events
Develops relationships with referring physicians
and ancillary departments
How You'll Work.
Team & Collaboration
close collaboration with the study team and investigator; Work effectively in a team environment, coordinating work flow with other team members
Communication Scope
communicate effectively with others; hear, understand and distinguish speech and other sounds
Process & Methodology
implementation of the study protocol, recruitment plan, study visits, data, study assessments
Applying for this Clinical Research Coordinator or Research Assistant role?
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