Greg Feitl Email & Phone Number

Stillwater, Mn

Chaska, Mn

Chaska, Mn

Chaska, Mn

Design, organize, and conduct complex internal and external clinical studies for new and improved products. Develop comprehensive clinical plans. Create clinical protocols. Design CRFs and eCRFs. Identify and contact potential investigators. Negotiate study budgets and financial payments. Ensure adequacy of clinical research staff/facilities. Site selection. Monitoring clinical studies consistent with GCP. Analyze the clinical data. Writing summary reports. Prepare technical articles for publication in professional journals and company literature.

University Of Minnesota

Facilitate the compliant execution of cancer clinical trials from protocol inception through study closure. Complete regulatory submissions to scientific review and IRB committees, and study sponsors and CROs. Create and adapt informed consents to comply with local and industry standards. Serve as liaison with sponsor, principal investigator, research coordinator, IRB, review committees, and monitors (internal and external) to gather additional documents/ information and address issues of study rationale, implementation, and safety monitoring. Manage regulatory documentation of affiliate research sites. Assist in the development and maintenance of regulatory standards. Maintain and apply current working knowledge of relevant federal, state, and local laws and regulations, and University policies regarding research activities. Create and maintain research documents and ensure all are filed and archived properly in accordance with regulatory agency requirements. Monitor trends in regulatory/protocol processes and make recommendations for improvement. Provide education, training, and serve as a resource to improve research compliance.

Plymouth, Mn

AGA Medical Corporation, Plymouth, MN. Design, monitor, and close out clinical investigations. Set up clinical research sites. Prepare and maintain manuals of operation, case report forms, informed consent documents, and other specialized clinical documents. Assist in development and maintain clinical research protocols. Lead interdisciplinary team meetings. Train staff and site personnel regarding research protocols and procedures. Prepare annual reports and assist in preparing progress reports to the FDA. Organize investigator, data safety monitoring board, and echo board meetings. Clinical forms and data review. Query generation and resolution. Conduct field audits to assure protocol compliance and data integrity. Process emergency and compassionate use cases. Generate presentations for meetings. Generate follow-up and IRB renewal reminder reports for investigators. Adherence to and review of standard operation procedures.

Bloomington, Mn

Design and create case report forms to ensure completeness and consistency with protocol requirements, as well as printing and maintenance of inventory. Write validation procedures, CRF guidelines, and data review guidelines. Perform clinical data review and discrepancy management. Coordinate data reviews and responsible for performing data audits to ensure accuracy of the clinical database. Review data tables, listings, annual reports, investigators’ brochures, study reports, and publications. Provide status reports to team members. Work with contract research organizations in managing outside data management processes. Organize and maintain data management study files. Adherence to and review of standard operating procedures.

Minneapolis, Mn

Manage and train research clinic staff for cardiovascular, genetic, and pharmaceutical studies. Develop and implement research protocols, manuals of procedure, and case report forms. Establish and manage clinical research site. Develop and manage project budgets for multi-center, collaborative research projects. Coordinate activities and direct communication between subcontracts of multi-center research studies. Conduct monitoring visits of collaborative agencies (research sites, laboratories, reading centers, and data coordinating centers). Develop and lead centralized training sessions. Organize meetings/conference calls and prepare official minutes. Prepare grant submissions and project update reports to funding agencies. Prepare and submit IRB human subjects approvals and develop informed consent forms. Manage data collection and data entry processes. Reconcile data queries. Database creation and management. Obtain informed consent and conduct clinical interviews. Report severe adverse events. Clinical data review. Establish methodologies for quality control and assurance. Train staff in human subjects and good clinical practices.

Minneapolis, Mn

Manage data collection and data entry processes. Clinical data review. Reconcile data queries. Database creation and management. Assist in managing clinical research studies. Obtain informed consent and conduct clinical interviews. Establish methodologies for quality control and assurance.

St. Paul, Mn

Managed ticket takers, ushers, and security personnel at stadium/arena/auditorium events. Responsible for accurate ticket counts for establishing precise attendance figures. Supervised stadium security and fan relations. Office duties.