Project Leader - Biostatistician

Overview Project Leader - Biostatistician US Remote Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose 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. In addition to successful completion of statistical leadership responsibilities, the PL-Stat is responsible for the above named project leadership activities as an integral contributor to project success. Responsibilities Accountable for technical, scientific, and fiscal execution of government research projects through collaboration with staff from multiple departments, including Clinical Operations, Biostatistics, Clinical Data Management, Clinical Data Systems, Program Management, IT, Web Development, Finance, Contracts, Regulatory, and Pharmacovigilance. 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. May provide performance-related feedback to department managers for project staff. 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. Proactively addresses client needs for ongoing studies and engages clients regarding new opportunities. 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 while considering client needs, budget, scope, and the research field. With team input, defines solutions that meet client needs within project-defined scope. Defines and approves approaches or solutions to project requirements, risks, and issues. Communicates risks and contingencies to clients and internal Government Delivery oversight. Develops, maintains, and secures approval of budgets, statements of work, and subsequent modifications prior to client distribution, as well as invoices and subagreements. Liaises with corporate leaders and other departments to ensure staff resources are informed, trained, and efficiently utilized to support execution of the project scope. Represents the project in Corporate meetings (e.g., project reviews) and provides central status reporting and information to Executive leadership, as applicable. 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. Models Emmes values of integrity, accountability, collaboration, innovation, and perseverance. Supports corporate knowledge expansion by participating in internal and external meetings/trainings and sharing insights and best practices with project teams, service groups, and other corporate stakeholders. Promotes and implements corporate initiatives, as directed. Leads or contributes to operational strategy development, budget preparation, and proposal content for new business opportunities. Represents Emmes at proposal meetings, business development activities, conferences, or other events, as requested. Performs other duties as assigned. Complies with all policies and standards. Qualifications Education/Requirements 6 years + Master's or 3 years + PhD of empirical knowledge of the key accountabilities/duties/responsibilities for the position with a typical tenure of at least 3 years project management experience in a research environment. Demonstrated working knowledge of the principles of clinical trial management and operations with at least 3 years of management experience in a research environment Project Delivery Track Record: Demonstratable track record of successfully delivering complex/high-priority clinical trials or clinical research projects within the agreed time, quality, and budget. Experience in federally-funded research is preferred. Clinical Research Knowledge: Demonstrated working knowledge of the principles of clinical research management and operations. Problem-Solving: Demonstrated strong problem-solving and analytical skills, combined with sound business and ethical judgment. 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. Highly motivated with the ability to work independently and as part of a multi-disciplinary team. Ability to supervise, mentor, and support lower-level project leaders and staff. 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 to influence and execute project decisions. Why work at Emmes? At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including: Flexible Approved Time Off Tuition Reimbursement 401k Retirement Plan Work From Home Anywhere in the US Maternal/Paternal Leave Casual Dress Code & Work Environment CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes The Emmes Company, LLC is an equal opportunity employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability or protected veteran status. #LI-Remote