Remote Study Manager II I
San Francisco Metro Area, CA 94588 US
A minimum of 5-8 years of Clinical project management experience within an IVD Clinical Trial environment including but not limited to:
- Work experience in research & development strongly preferred
- Work experience in clinical operations strongly preferred
- Work experience in standard project management processes strongly preferred
- Work experience in a regulated Diagnostic, Medical Device, Pharmaceutical Industry strongly preferred
Manages Clinical Operations and Biometrics (COBM) related project information to support decision making by project teams, COBM Leadership Team, Life Cycle Teams (LCTs) and Life Cycle Committee (LCC). Applies project management skills and clinical operations experience to deliver projects on time, within budget and with high customer satisfaction. Assigned projects may include multiple Roche Molecular Solutions (RMS) Business Units (BUs), involve collaboration with other COBM Clinical Project Managers (cPMs), global BU Project Management Offices (PMO) Project Managers (PMs) and/or global PMO Leadership.