Clinical Study Manager/Principal CRA
Sterling Life Sciences - San Francisco, CA

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1) Coordinate and supervise all aspects of a clinical study 2) Monitor clinical trial sites 3) Assist Clinical Program Manager in overall study management 4) Draft and coordinate review of relevant documents, including protocols, informed consents, case report forms, monitoring plans, investigator brochures and clinical study reports 5) Maintain study timelines 6) Contribute to development of study budget and RFPs and participate in selection of CROs/vendors 7) Manage CROs/vendors 8) Coordinate review of data listings and preparation of interim/final clinical study reports 9) Contribute to development of abstracts, presentations and manuscripts 10) Ensure effectiveness of site budget/contract process 11) Participate in meetings and conference calls with CROs, vendors and multi-functional teams 12) Train CROs, vendors, investigators and study coordinators on study requirements 13) Assist in determining the activities to support a project's priorities within functional area 14) Design scientific communications within the company, under supervision
1) University degree is required (preference will be given to those with degree in relevant field, though all candidates are welcome and encouraged to apply)2) Appropriate full-time work experience is mandatory (no students or fresh graduates please)3) Recent experience in the biopharmaceuticals industry is strongly preferred4) Preference will be given to people who have recent experience in Clinical Study Management