Senior Industrial Designer

Johnson & Johnson

(Boston, Massachusetts)
Full Time
Job Posting Details
About Johnson & Johnson
Caring for the world, one person at a time, inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people.
Responsibilities
Responsible for managing the planning, implementation, and tracking of clinical projects and activities. Maintains an overview of the clinical trials and their integration into a registration package. At this level, the position has a greater degree of impact on the business results and typically, responsibility for managing a group of professionals Participates in protocol development, case report form design, project plans creation and clinical report writing. Negotiates and prepares project budgets. Reviews weekly status reports on all aspects of progress of the projects and addresses problems, guides the troubleshooting process. Gathers, analyzes and prepares a summary overview to the appropriate management on the status of studies. Ensures that standard operating procedures are reviewed regularly, and remain relevant and adhered to. Recommends policies, procedures and processes to ensure that a high level of quality control and quality assurance is maintained. Participates in development and harmonization of standard operating procedures and departmental procedures. Prepares presentation material for investigator meetings. Manages clinical trials outsourcing activities and maintains ongoing communication of operation issues between vendors, sites and company.
Ideal Candidate
**Education /Training background:** * MD. is mandatory; MSc. or PhD is an asset. **Knowledge/Skills:** * Thoroughly understand and command knowledge of product and relevant diseases * Solid knowledge of clinical development process and HA (especially SFDA) requirements * Thoroughly understand and command GCP * Thoroughly understand and command HCC **Job experience:** * At least 3-year clinical practice in relevant therapeutic area/or 5-year working experience in pharmaceutical industry (especially clinical development, and people management) is preferred **Competency:** * Strategic and creative thinking capabilities; keen clinical development insight; excellent communication and team collaboration skills; leadership capabilities. **Others:** * excellent english ablities of listening, speaking, reading and writing; same level of CET-6

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