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[Hiring] Project Leader - Biostatistician @Emmes Group

100% remote Flexible hours Hiring now

Role Description The Project Leader - Biostatistician (PL-Stat) is critical to the successful conduct of government-sponsored clinical research projects, serving as the matrix leader of the core project team. In addition to serving as study Biostatistician, the PL-Stat is accountable for successful delivery of clients' statement of work activities within timeline and budget. The PL-Stat develops and maintains a positive relationship with clients and other external stakeholders, oversees deliverable quality, mentors staff, and works collaboratively across departments to accomplish project goals. The PL-Stat is responsible for the continuous monitoring, identification, escalation and mitigation of project risk.

  • Accountable for technical, scientific, and fiscal execution of government research projects through collaboration with staff from multiple departments.
  • Perform statistical duties per statistical JDs level/experience and project SOW.
  • Sets priorities for the project team, ensures quality processes are followed, and collaboratively establishes and maintains deliverable timelines.
  • Identifies statistical issues, proposes solutions, and consults with other statisticians across the company on project-related statistical matters.
  • Serves as the primary point of contact for clients, investigators, and other stakeholders for assigned projects and/or protocols.
  • Develops, reviews, and approves project plans, study documents, and processes/SOPs, as needed.
  • Applies broad knowledge of therapeutic areas, clinical trial design, and process expertise to influence and execute project decisions.
  • Defines and approves approaches or solutions to project requirements, risks, and issues.
  • Develops, maintains, and secures approval of budgets, statements of work, and subsequent modifications prior to client distribution.
  • Liaises with corporate leaders and other departments to ensure staff resources are informed, trained, and efficiently utilized.
  • Represents the project in Corporate meetings and provides central status reporting and information to Executive leadership.
  • Uses key performance metrics to effectively execute the project scope.
  • Mentors project staff and supports staff development; may contribute to the development of new Project Leaders.
  • Supports corporate knowledge expansion by participating in internal and external meetings/trainings.
  • Promotes and implements corporate initiatives, as directed.
  • Leads or contributes to operational strategy development, budget preparation, and proposal content for new business opportunities.
  • Performs other duties as assigned.
  • Complies with all policies and standards.

Qualifications

  • 6 years + Master's or 3 years + PhD of empirical knowledge of the key accountabilities/duties/responsibilities for the position.
  • Demonstrated working knowledge of the principles of clinical trial management and operations.
  • Project Delivery Track Record: Demonstratable track record of successfully delivering complex/high-priority clinical trials or clinical research projects.
  • Clinical Research Knowledge: Demonstrated working knowledge of the principles of clinical research management and operations.
  • Problem-Solving: Demonstrated strong problem-solving and analytical skills.
  • Communication: Excellent verbal and written communication skills for client, team, and scientific interactions.
  • Leadership & Teamwork: Ability to work proactively and effectively, with creative problem-solving and collaboration skills.
  • Project Management: Strong cross-functional project management and time management skills.
  • Therapeutic Expertise (Preferred): Broad understanding of a therapeutic area, clinical trial design, and/or process expertise.

Benefits

  • Flexible Approved Time Off
  • Tuition Reimbursement
  • 401k Retirement Plan
  • Work From Home Anywhere in the US
  • Maternal/Paternal Leave
  • Casual Dress Code & Work Environment

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