• Clinical Trials Monitor - Neuro-Oncology

    Location US-MA-Boston
    Job Posted Date 2 weeks ago(10/30/2018 1:54 PM)
    Job ID
    2019-13001
    Category
    Clinical Research
    Type
    full time
    Grade
    21
  • Overview

    Located in Boston and the surrounding communities, Dana-Farber Cancer Institute brings together world renowned clinicians, innovative researchers and dedicated professionals, allies in the common mission of conquering cancer, HIV/AIDS and related diseases. Combining extremely talented people with the best technologies in a genuinely positive environment, we provide compassionate and comprehensive care to patients of all ages; we conduct research that advances treatment; we educate tomorrow's physician/researchers; we reach out to underserved members of our community; and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.

    The Clinical Research Specialist performs, coordinates, and monitors all aspects of the regulatory process within clinical trials in accordance with Good Clinical Practice, institutional policies and procedures, and research protocols.  Conducts site visits to determine protocol and regulatory compliance, and prepares required documentation.  Responsible for multiple projects and must work both independently and in a team environment.  May participate in protocol and study development and start up processes including reviewing protocols, designing and/or reviewing Case Report Forms, preparing informed consent documents, developing study specific source document worksheets, and working with study team management on operational strategies.

    Responsibilities

    • Assist in the development and writing of clinical trial protocols.
    • Liaise with investigators and disease groups on conducting clinical trials.
    • Prepare and manage regulatory applications to federal and local agencies (FDA, OHRS, etc.) and the related approval process.
    • Locate and/or assess the suitability of study sites to conduct clinical trials.
    • Monitor trial progress throughout its duration which may include visiting study sites on a regular basis.
    • Verify that data entered on the Case Report Form is consistent with patient clinical notes and other source documentation (source data verification).
    • Act as a regulatory resource for study sites by maintaining regular contact with investigators and study teams during the course of studies to ensure that compliance is maintained.
    • Prepare reports as required regarding the status of ongoing studies and make necessary recommendations for contingency planning.

    Qualifications

    • BS/BA degree required; Master’s preferred. 

    • Minimum of 5 years clinical research experience with oncology background preferred.

    • Requires excellent verbal and written communication skills with an in-depth knowledge of GCP guidelines, medical terminology, and the clinical trial process.  

    • In addition, excellent interpersonal skills with strong organizational skills and an attention to detail are needed.  

    • Must be computer literate and be able to travel depending on project needs.



    Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other groups as protected by law.

    Options

    Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
    Share on your newsfeed

    Connect With Us!

    Not ready to apply? Connect with us for general consideration.