UP Health System – Marquette

Performs a variety of duties to support administration of the assigned department(s).

Coordinates protocols, including subject screening, recruitment, consent, enrollment, implementation, monitoring, and follow-up of research procedures in several acute clinical trials.
Maintains, Administers, and monitors Investigational Study Agents/Device Accountability, and research supplies.
Develops study tools for performing study requirements effectively per protocol.
Documents all study-related procedures/adverse events, including the maintenance of research records, completes case report forms and perform electronic data entry.
Prepares regulatory submissions to the Institutional Review Board and work with monitors/auditors to resolve data queries and ensure data accuracy.
Promotes good clinical practices in the conduct of clinical investigations by possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection.

Job Requirements:

Minimum Education
  • Graduated from a Nursing program required
Required Skills
  • Requires critical thinking skills, decisive judgment and the ability to work with minimal supervision. Must be able to work in a stressful environment and take appropriate action.
  • Licensed Practical Nurse (LPN) in State of Michigan if graduated from LPN program required
  • Registered Nurse (RN) in State of Michigan if graduated from RN program required
  • Basic Life Support Health Care Provider (BLS-HCP) required
Minimum Work Experience
  • 5 years healthcare experience required
  • 1 year research experience preferred

Equal opportunity and affirmative action employers and are looking for diversity in candidates for employment: Minority/Female/Disabled/Protected Veteran

To Apply: https://www.jobg8.com/Traffic.aspx?wOgvsyO7BI8c7umvanfKlAz