General Manager jobs in the Biotech, R&D, Science category at Smith Hanley Consulting Group

Job Description: QA Program Manager Contract: 6 Months - Permanent Hire Bachelor’s degree + 4years experience Relocation Available The QA Manager will be responsible for setting up a non-existent QA Program. Individual will be directing our QA group in developing metrics and determining work load. Provide insight as to how to review the literature and pull into and customize. Successful candidate ...
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Job Description: The CEP (Customer Engagement Programs) Review and Remediation Project Manager will support the global project for assessment, review, and remediation of CEPS by tracking and coordinating activities related to this project. This role reports to the CEP BPO Key Responsibilities • Create a process to track and prioritize review and remediation activities that arise from the Global MQ...
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This position reports into Head of Global Sourcing Area and works within Procurement across legal entities and national boundaries with a strong focus on procurement strategy and service delivery. This position would provide contract support within a therapeutic or division specialty. This position will also support the identification, selection, and management of suppliers and contracts across th...
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Minimum Requirements • University Degree or equivalent • A specialist knowledge of contract and procurement management, with specific reference to the pharmaceutical/health care industry. • A demonstrated knowledge of contracting/commercial processes preferably from the CRO industry • A good understanding of procurement and project management tools and processes. • Comprehensive knowledge of clini...
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The Sr. Clinical Research Coordinator will, in collaboration with the Senior Clinical Manager(s) oversee the appropriate conduct of clinical trials being conducted within their assigned Group. This will include, but not be limited to subject participation activities, maintenance of protocol data, oversite of adherence to protocol specifics as well as specific regulatory functions. The Sr. CRC will...
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REQUIRED • Must be Pharm.D. with 3-5 years pharmaceutical industry experience or relevant clinical experience DESCRIPTION • Participate in ongoing comprehensive product/disease area training to serve as Medical Information expert within area of responsibility • Ability to communicate on professional level with physicians, nurses, pharmacists, and other professional staff when discussing products. ...
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Job Description: · Support company internal customers in the development of outsourcing requirements for Phase I-IV global clinical trials · Lead and support the qualification and evaluation process for new service providers · Lead the process of Request for Proposal (RFP) development from service provider selection through final contract execution · Manage the contracting process including prepar...
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