Description
JOB SUMMARY:
Provide cross-site support to the Research Operations Manager in areas of project management, budgeting, outsourcing studies, and operational support to all CBSS departments.
FUNCTIONS (Duties/Accountabilities)
Assist the Research Operations Manager and cross-site departments in timeline management, budgeting, outsourcing studies, invoice creation and payment, report creation and distribution, and ERP support. Create and update Tox plans, APECS templates and APECS timelines to support in-house, outsourced, and Investigative Toxicology studies. Assist in generating and verifying the preclinical Master Schedule to ensure compliance with GLPs. Prepare and distribute customized reports for CBSS Sr. Management and staff. Create and maintain business practices and SOPs for CBSS Operations. Organize and interpret project data and/or business process work flows for broader audiences. Serve as team representative on various cross functional teams. Interact effectively with internal and external pre-clinical study personnel to plan and maintain study timelines and budgets. Attend pre-study meetings with scientific staff to ensure study timelines and protocols adhere to appropriate timeline template standards. Interact with finance personnel and GLP compliance staff to ensure accurate forecasting of study accruals and projected timing of studies.
Requirements
Basic Qualifications:
Bachelor's degree in project management, computer science, or life sciences. Minimum 2 years work experience in project management, computer science, or life sciences.
Preferred Qualifications:
Master's degree or MBA in project management, computer science or toxicology.
Two or more years experience in the pharmaceutical industry; previous Amgen experience desirable. PMI certification preferred.
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