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  1. Reporter

    We currently have several opportunities for reporters to join our NYC editorial team!   On a typical day reporters at Law360 will file four stories.  These stories cover a wide array of practice areas, including employment law, environmental law, intellectual property law and securities law; and most recently, mergers & acquisitions, private equity, real estate, project finance, and capital markets; in industries such as energy, financial services, health-care, media and technology.   ...

  2. Corporate Director of Organizational Development

    Axion is currently looking for a Corporate Director of Organizational Development for a perm position in the Bronx.  The salary is $135-165k.  Job description is as follows: JOB PURPOSE: Acts as Organizational Development liaison and advisor to clients leadership and facilitates clients initiatives across the enterprise. Oversees and monitors interventions and learning activities conducted by training and learning vendor. Plans, develops, implements and administers HR programs for clients employees. ...

  3. Attorney, Director, Commercial and Regulatory Counsel

    A bio pharmaceutical company based in Central CT, is seeking an attorney with: 6+ years experience as a practicing attorney, with at least 3 years' experience in the pharmaceutical/biotech industry. Significant legal experience in fraud and abuse counseling and FDA issues, with a working understanding of the OIG’s Guidance for the Pharmaceutical Industry, applicable regulations and laws relating to the development, sales and marketing of pharmaceutical products, the enforcement landscape from a U.S. ...

  4. Quality Manager Clinical Trials - Tarrytown, NY

    Plan and conduct GCP audits, issue audit reports, recommend corrective action and conduct follow up to audits and corrective actions for a company currently involved in several clinical trials Shall assist in preparing investigational sites for FDA inspection, review and recommend compliance related policies and procedures and evaluate impending regulations, guidelines and industry standards and their impact on the clinical trials and the company. Must possess at least 5 years experience in ...