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  • Senior Program Manager- Interventional Studies in Aging Center (ISAC) at the Institute for Aging Research

    Job Locations US-MA-Roslindale
    Job ID
    2018-2409
    Category
    Research/Medicine
  • Overview

    The Interventional Studies in Aging Center (ISAC) at the Institute for Aging Research (IFAR) is seeking a Senior Program Manager to work with the Directors in growing all aspects of ISAC.  The Senior Program Manager will provide support to investigators conducting clinical trials. This is an exciting and visible opportunity for an experienced professional to take on a key role at IFAR, one of the leading research institutes in the field of aging. The position will include program development and project management related to human investigations in aging.

    Responsibilities

    • Manage key administrative and programmatic processes within ISAC including carrying out the strategic plan for building a new clinical trials center focused on healthy aging
    • Coordinate communications and outreach for ISAC events (i.e. seminars and teaching workshops) within IFAR
    • Coordinate consultation services provided by ISAC faculty and staff to investigators
    • Manage solicitation and administrate the pilot study program
    • Guide investigators through project management and regulatory issues faced with clinical trials
    • Collaborate with ISAC team members on development and testing of data capture, management and analysis tools
    • Lead by example by serving as project manager on one or more active projects

    Qualifications

    • Minimum 3-5 years of experience in the management and execution of clinical trial operations, preferably multi-site investigations in older populations
    • An advanced degree (e.g., Master’s, NP, PA-C, PhD, MD) in clinical research, medicine, nursing, psychology, sociology, epidemiology or a related discipline required
    • Certified in Good Clinical Practice; comprehensive understanding of regulatory requirements in human subjects research; familiarity with ICH guidelines, 12 CFR Part 11 and other relevant regulatory requirements
    • Experience with IND applications and interactions with the FDA is considered an asset
    • Solid knowledge and experience in state-of-the-art clinical trial project management
    • Soft skills: collaboration, independence, ambition, pragmatism, able to communicate to scientific and lay audiences in English
    • Desire to participate as a leader in a growing biomedical research organization;
    • Outstanding organizational skills; ability to lead, take instruction and adapt to change
    • Independent thought and ability to execute and share ideas with confidence

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