Clinical Research Administrator
Clinical Operations Manager (2), Immune Tolerance Network, University of California at San Francisco, San Francisco, California
Submitted by Roger Evans on Fri, 01/07/2011 - 00:34.Clinical Operations Manager (2), Immune Tolerance Network, University of California at San Francisco, San Francisco, California
Description:
The Clinical Operations Manager will lead, direct, and coordinate the operational efforts in the development and implementation of research-driven, investigator-initiated clinical trials, supported and conducted by the Immune Tolerance Network (ITN) at UCSF and sponsored by the National Institutes of Health (NIH); ensure the efficient conduct of all activities from protocol development through completion of the trial; assemble and lead the multidisciplinary study management team charged with establishing the project goals for protocol development and trial implementation by preparing and/or reviewing all trial-related documents and budgets, planning and documenting trial activities, providing CRO/vendor management, and clinical trial site management; and perform other duties as assigned.
Required Qualifications:
BA/BS in a health-related science or RN or a related field and six years of experience in administrative analysis or operations research; or an equivalent combination of education and experience; 5 years of experience in clinical research, clinical coordinator, clinical nurse role; in-depth knowledge of FDA/ICH guidelines and significant experience managing clinical trials in academic clinical research or pharmaceutical/biotechnology company; expert knowledge of MS Office Suite; Working knowledge of MS Project; knowledge and experience with medical and scientific terminology and concepts; effective communication and interpersonal skills; demonstrated ability to prioritize and multitask to meet multiple deadlines; work independently and as part of a team; fluency in English (verbal and written).
Preferred Qualifications:
Clinical Trials Professional certification; clinical trials project management experience; knowledge of UC/UCSF and NIH policies and procedures; experience in Diabetes, Allergy, Autoimmune Disorders, or Transplant.
Contact:
This is a courtesy position posting. Please contact Dr. Evans by e-mail or telephone 507-206-3700 for additional information as to whom you should contact to apply. All inquiries are strictly confidential.
Identifiers:
Main Category: Research
Subcategory: Clinical Research Administrator
TPDC Position ID: CASF-2011-0006
Position ID or Job Requisition No: 34503BR
UNOS ID or Other ID: CASF
City: San Francisco
State/Province: California
Country: USA
Date Posted: 01-07-11
Clinical Operations Manager (1), Immune Tolerance Network, University of California at San Francisco, San Francisco, California
Submitted by Roger Evans on Fri, 01/07/2011 - 00:32.Clinical Operations Manager (1), Immune Tolerance Network, University of California at San Francisco, San Francisco, California
Description:
The Clinical Operations Manager will lead, direct, and coordinate the operational efforts in the development and implementation of research-driven, investigator-initiated clinical trials, supported and conducted by the Immune Tolerance Network (ITN) at UCSF and sponsored by the National Institutes of Health (NIH); ensure the efficient conduct of all activities from protocol development through completion of the trial; assemble and lead the multidisciplinary study management team charged with establishing the project goals for protocol development and trial implementation by preparing and/or reviewing all trial-related documents and budgets, planning and documenting trial activities, providing CRO/vendor management, and clinical trial site management; and perform other duties as assigned.
Required Qualifications:
BA/BS in a health-related science or RN or a related field and six years of experience in administrative analysis or operations research; or an equivalent combination of education and experience; 5 years of experience in clinical research, clinical coordinator, clinical nurse role; in-depth knowledge of FDA/ICH guidelines and significant experience managing clinical trials in academic clinical research or pharmaceutical/biotechnology company; expert knowledge of MS Office Suite; Working knowledge of MS Project; knowledge and experience with medical and scientific terminology and concepts; effective communication and interpersonal skills; demonstrated ability to prioritize and multitask to meet multiple deadlines; work independently and as part of a team; fluency in English (verbal and written).
Preferred Qualifications:
Clinical Trials Professional certification; clinical trials project management experience; knowledge of UC/UCSF and NIH policies and procedures; experience in Diabetes, Allergy, Autoimmune Disorders, or Transplant.
Contact:
This is a courtesy position posting. Please contact Dr. Evans by e-mail or telephone 507-206-3700 for additional information as to whom you should contact to apply. All inquiries are strictly confidential.
Identifiers:
Main Category: Research
Subcategory: Clinical Research Administrator
TPDC Position ID: CASF-2011-0005
Position ID or Job Requisition No: 34610BR
UNOS ID or Other ID: CASF
City: San Francisco
State/Province: California
Country: USA
Date Posted: 01-07-11
