Established • Co-Founded • and Manage OutReach Research Site of B... • Minnesota (founded-December 2006)* *Foun... • monitor • coordinate • and manage an out-reach Clinical Researc... • screening and enrolling subjects for cli... • medication administration and instruction • and safety visits Phlebotomy • processing and shipping of labs IATA... • EDC Maintain source documents and re... • Guideline • protocol and FDA/regulatory compliance ... • training requirements • safety practices and company policies. ...
Aug 2014 to 2000 Certified Clinical Research CoordinatorMinneapolis Heart Institute Foundation
Dec 2006 to 2000 CCRC/Research AssociateRadiant Research Edina, MN Aug 2004 to Jun 2005 Research CoordinatorAnchor Research Naples, FL Apr 2002 to Jun 2003 Research CoordinatorPrivate Duty Nursing Naples, FL Oct 2001 to May 2002 Private Duty CargiverMarriott Brighton Gardens Naples, FL Sep 2001 to Feb 2002 LPN, SupervisorSt. Cloud Hospital
1996 to 2001 LPN-Staff
Education:
St. Cloud Technical College Saint Cloud, MN 1993 to 1995 LPN in NursingSt. Cloud State University General Studies of Continuing Education
Skills:
Established, Co-Founded, and Manage OutReach Research Site of Baxter, Minnesota (founded-December 2006)* *Founded, monitor, coordinate, and manage an out-reach Clinical Research Site for Minneapolis Heart Institute Foundation. I am involved in many aspects of clinical research studies for local and non- local patients including Start-up to close-out Follow-up visits Recruitment, screening and enrolling subjects for clinical trials Obtain informed consent and continued process Conduct study visits including protocol procedures: EKGs, medication administration and instruction, and safety visits Phlebotomy, processing and shipping of labs IATA/Hazmat Complete case report forms, EDC Maintain source documents and regulatory documents Prepare institutional review board and institutional bio-safety committee submissions and reports. Monitor site activities during the study to ensure GCP, Guideline, protocol and FDA/regulatory compliance Perform source document verification Ensure completeness of all essential regulatory documentation Build and maintain positive relationships with the sponsor and investigators. Produce regular communications to encouraging proper completeness Detail oriented; ability to prioritize and manage multiple tasks; ability to manage multiple studies Knowledge of medical terminology Adhere to and promote proper practices and techniques which are consistent with current operating procedures, training requirements, safety practices and company policies. Train physicians and staff to protocol and educate patient population to research CITI train assurance of all persons involved with the conduct of site trials.
Melbourne Australiamulticulturalarts victoria Jill Morgan has worked extensively in multicultural and indigenous arts in Australia. Jill is presently the Executive Officer of Multicultural Arts Victoria and... Jill Morgan has worked extensively in multicultural and indigenous arts in Australia. Jill is presently the Executive Officer of Multicultural Arts Victoria and was previously the Executive Director of Kulcha, Multicultural Arts of Western Australia.
Jill Morgan of Poway said 11 of her family members who live in various different counties have recently tested positive as have she and her husband. Both, she said, made it through the entire pandemic and the following years of relative calm without getting sick.