• Clinical Data Operations Project Manager

    Job ID
    13856
    Type
    Regular Full-Time
    Company
    Fred Hutchinson Cancer Research Center
    Location
    US-WA-Seattle
    Category
    Biostatistics, Bioinformatics and Computational Biology
  • Overview

    Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first and largest cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network (HVTN). Careers Start Here.


    The Biostatistics, Bioinformatics and Epidemiology (BBE) program in the Vaccine & Infectious Disease Division (VIDD) is seeking a Data Operations Project Manager to manage clinical research data-related projects and deliverables in collaboration with BBE faculty and external collaborators evaluating vaccines to prevent HIV, Tuberculosis and other infectious diseases.

     

    Some travel, including international travel, may be required. (less than 10% time). Flexible work hours required due to occasional international conference calls.

    Responsibilities

    The Data Operations Project Manager will apply knowledge of clinical data management & research operations to

    • Prioritize and monitor data operations activities, ensuring that research needs and time lines are met.
    • Serve as a liaison with internal project teams and external organizations.
    • Define and track deliverables, budgets, milestones, and timelines for new and existing research projects.
    • Review project plans and data specifications to identify discrepancies and inconsistencies.
    • Coordinate and oversee the investigation and resolution of data discrepancies.
    • Manage projects, plan and facilitate meetings, and document activities described above.
    • Perform other tasks related to study data management operations, as required.

    Qualifications

    Required:

    • Bachelor's degree in biological science-related field
    • Five years of related experience in a research setting
    • Strong interpersonal and organizational skills
    • Excellent written and verbal communication skills
    • Experience with Microsoft Office suite, especially Word and Excel
    • Experience working with clinical trial data in a multidisciplinary team environment
    • Experience reading and writing technical documents
    • Experience managing projects with multiple stakeholders
    • Critical thinking skills and collaborative approach to problem solving


    Desired:

    • Experience with and knowledge of clinical trial data entry and management systems (e.g. Medidata Rave)
    • Familiarity with CDISC data standards
    • Experience managing budgets
    • Experience with Business Intelligence software (e.g. Power BI, Tableau)

    Our Commitment to Diversity

    We are committed to cultivating a workplace in which diverse perspectives and experiences are welcomed and respected. We are proud to be an Equal Opportunity and VEVRAA Employer. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability, marital or veteran status, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We are an Affirmative Action employer. We encourage individuals with diverse backgrounds to apply and desire priority referrals of protected veterans. If due to a disability you need assistance/and or a reasonable accommodation during the application or recruiting process, please send a request to our Employee Services Center at escmail@fredhutch.org or by calling 206-667-4700.

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