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    Sr Clinical Program Manager - Fishers, United States - Pintail Solutions

    Pintail Solutions
    Pintail Solutions Fishers, United States

    2 days ago

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    Description

    Job Description

    Job DescriptionJOB DESCRIPTIONJob TitleSr. Clinical Program ManagerPosition TypeFull timeLocationremoteTravel RequiredSome travel requiredExternal Posting URLApplications Accepted ByAudra Miller
    Mail:
    Audra Miller
    Pintail Solutions, Suite 1040
    12175 Visionary Way
    Fishers, IN 46038Job DescriptionOverview
    Pintail Solutions is an accomplished advisory firm in the life sciences industry across pharma, biotech and technology companies as well as higher education and non-profit organizations. We specialize in providing services for complex projects to help improve global health. We're passionate about delivering innovative solutions and sustainable plans for an organizations most intricate challenges. Pintail Solutions offers a dynamic work environment, grounded in the entrepreneurial offices of Launch Fishers in central Indiana.

    The Senior Clinical Program Manager will be focused on partnering with a large renowned academic research institution on government funded global clinical trials. Qualified candidates will have 15+ years experience leading global clinical trials and a strong understanding of FDA regulations and processes.

    This individual(s) will need an entrepreneurial spirit, deep project management and planning experience in both industry as well as academia. Candidates must have a mature business perspective to engage with internal and external business partners.

    The following roles and responsibilities entail most of what these roles may require, but may expand based on the individual and organizations needs.

    Roles and Responsibilities
    Project Management
    • Candidates should have a strong background in project/program management within clinical trials, pharma, biotech, academic research and regulatory processes.
    • Ability to lead global, FDA regulated trials.
    • Experience in all phases of clinical research.
    • Ability to liaise with leadership and PM teams on integrated planning and detailed project plans including deliverables, milestones, timelines, risks, capabilities needed and budget.
    • Ability to identify and deliver process improvement and documentation where needed to further enable success across the institution.
    • Ability to mentor and train junior pm staff to elevate experience within the organization.

    Communication
    • Effectively communicate across all levels of the organization.
    • Liaise both internally and externally on project deliverables, solving challenges and issues.
    • Drive operational meetings including agendas, facilitation, meeting minutes etc.
    • Ensure seamless communication across the entire program.
    • Ability to influence decision making and issue resolution across the organization.

    Vendor Management
    • Research, identify and potentially qualify vendors.
    • Communicate and manage vendor relationships.
    • Partner and engage with vendors to direct work across projects.

    Qualifications and Education Requirements
    Candidates should have a 4-year college degree and a minimum of 10+ years project management experience within pharma, biotech, academic research etc. leading preclinical through Phase IV clinical trials. Candidates should be demonstrated in leading others through influence and be technically savvy.

    Preferred Skills
    Candidates will need to thrive in a dynamic, service-minded, entrepreneurial environment and have a consultant mentality. Abilities to make immediate impact are necessary. Mature and effective communication skills and business acumen are key to success.

    Additional Notes
    This role is expected to be full time and remote.
    • Some travel may be required

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