OMNI Human Resource Management

  • Director, Biostatistics

    Job ID
    2018-2169
    Client
    Altasciences Clinical Research
    Job Location(s)
    US | CA
  • Overview

    Altasciences- Vince and Asso

    Do you want a fast-paced, exciting and innovative career in research? Altasciences Preclinical Services is hiring a full-time Director, Biostatistics to be located anywhere in the US or Canada.

     

    Altasciences Preclinical Services encompasses Algorithme Pharma in Montreal, QC, Vince & Associates Clinical Research in Overland Park, KS, and Algorithme Pharma USA in Fargo, ND. One of the largest early phase clinical research organizations (CROs) in North America, Altasciences focuses on supporting early-stage drug development, providing clinical services to an international customer base of biopharmaceutical companies. With full-services solutions including clinical pharmacology, medical writing, biostatistics, data management and bioanalysis, the approximately 1,000 Altasciences medical/scientific field team members work together to contribute to the advancement of pharmaceutical science.

     

    Working in conjunction with the Biostatistics department, the Director, Biostatistics will oversee the Biostatistician function of all Altasciences clinical studies.

     

    DP-IND

    Responsibilities

    • Manage and execute all statistical aspects of clinical studies, such as statistical input into study design, sample size analysis, Statistical Analysis Plan, and analysis/interpretation of results
    • Develop and implement training curriculum/programming for all aspects of the Biostatistician role
    • Ensure quality client and internal deliverables and associated communications/reports
    • Collaborate with team members to ensure timeline adherence within the Biostatistics Department
    • Collaborate and consult with clients and leaders, providing study design and statistical expertise
    • Strong working knowledge of federal regulatory guidelines (TPD, FDA, EMA), adapting statistical methods and programs which comply with such guidelines
    • Strong working knowledge of CDISC deliverables
    • May be assigned direct reports

    Qualifications

    • Minimum of 7 years CRO related Biostatistics experience- working in all aspects of a full-service Biostatistics Department
    • MSc. or higher-level statistics degree or equivalent fields/experience
    • Working knowledge of SAS programming and CDISC implementation
    • Preferred Phase 1 clinical research experience, including Human Abuse Potential studies
    • Ability to communicate effectively, to correctly and accurately explain the statistical methods, data analyses and application of software
    • Proficient spoken/written English

    Our client has a strong commitment to their associates, clients and community. They offer an excellent compensation and benefits package and a unique culture.

     

    OMNI and our clients are Equal Opportunity Employers and seek diversity in candidates for employment. EEO Employer W/M/Vet/Disabled/Sexual Orientation/Gender Identity.

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