Research Scientist: International Surveillance Epidemiologist

Department

Epidemiology

Location

London, United Kingdom

Requirements

  • Experience in epidemiology research and practical applications. Prefer some experience with establishment and research in disease surveillance.

  • Excellent written and oral communication skills; good organizational and planning skills; effective presentation skills for a variety of audiences.

  • Strong computer skills, including working knowledge of epidemiological and safety databases.

  • Ability to build positive and productive professional relationships.

  • Knowledge and experience obtained through completion of a Ph.D. in Epidemiology.

  • Minimum of 2 years of epidemiology research experience

  • Global/international experience is preferred.

  • Fluent in English

    Responsibilities

  • Provide documentation of all work activities as part of assigned project information files.

  • Documentation of activities and contacts as part of business development activities.

  • Tracking and accountability for epidemiology portion of project budgets

  • Maintain appropriate allocation of time contributions to projects, business development and other company activities.

  • Continually seek process and operational improvements to increase value of epidemiology to business and individual projects

  • Effectively support, communicate, and adhere to all Company policies.

  • Development and management of international system for monitoring drug adverse events based on Registrat-Mapi disease area networks.

  • Serve as epidemiologist for global and local (US or Europe) projects.

  • Provide support in development of study designs, protocols, and CRFs and statistical analysis plans. Although analytic support will be provided, hands-on analytic skills would be preferred.

  • Prepare study reports and scientific manuscripts, and be able to present that work to clients and professional organizations in public settings

  • Provide input into the development of risk management and pharmacovigilance programs for sponsors in response to regulatory mandates.

  • Participate as an active member of multidisciplinary study teams to successfully achieve study and corporate goals.

  • Establish and maintain professional working relationships among Sponsors, Scientific Advisory Groups, and participating investigators.

  • Participate in business development activities, including product and therapeutic area research, literature searches, support for proposal development, client presentations, strategic consulting, and bid defenses.

  • Project management and execution of consulting projects including literature reviews, meta-analyses and healthcare database projects.

  • Actively participate in professional meetings and industry conferences to enhance both individual and REGISTRAT-MAPI’s reputation in the industry and maintain current professional knowledge

  • Reports to Vice President, Epidemiology, Drug Safety, Risk Management

  • Domestic and international travel as required.

    To contact Human Resources please click here. Or, feel free to contact us at:

    REGISTRAT-MAPI
    2343 Alexandria Drive, Suite 100
    Lexington, KY 40504.3276
    Tel: 859.223.4334
    Fax: 859.514.4350