Senior Director, Biostatistics, Clinical Operations
About The Position
AskBio Inc., a subsidiary of Bayer AG, is a gene therapy company focused on developing life-saving medicines. The company has a portfolio of clinical programs in various disease areas and a pipeline of investigational therapeutics. AskBio's gene therapy platform includes Pro10™ manufacturing process and an extensive array of capsids and promoters. The company's vision is to pioneer science for transformative molecular medicines, and its mission is to lead innovative science and drive clinical outcomes to transform lives. AskBio operates with principles of advancing innovative science, bringing transformative therapeutics to patients, and providing an environment for employee growth. Their values include being a Pioneer, Cultivating Collaboration, Embracing Responsibility, Raising the Bar, and Acting with Uncompromising Integrity. The Senior Director, Biostatistics, will provide technical leadership and operational oversight for clinical strategies, and the design, implementation, and reporting of non-clinical, CMC, and clinical development programs and studies. This role involves peer review of clinical trial designs and reports, collaboration with cross-functional teams, guidance to statisticians, support for regulatory interactions, and serving as the statistical representative in global drug approvals. This is a US hybrid position based in RTP, NC, Philadelphia, or Ohio, reporting to the Head, Biometrics, Clinical Operations.
Requirements
- Ph.D. or M.S. in Statistics or a related field.
- 10+ years of pharmaceutical experience in a pharmaceutical or biotech R&D environment.
- Knowledge of cardiovascular, metabolic, kidney, CNS, and/or rare disease programs.
- Previous experience preparing and submitting New Drug Applications to regulatory agencies.
- Strong knowledge of design of experiments, clinical trial design concepts or CMC statistics, drug regulation, and management of the statistical function.
- Extensive experience with SAS and/or R.
- Excellent communication skills.
- Experience in CRO selection, contracting, and management.
- Excellent leadership and interpersonal skills, with the ability to build credibility and trust inside and outside the Company.
Nice To Haves
- Experience with adaptive and Bayesian study design simulation techniques.
- Experience in rare diseases and/or gene therapy.
Responsibilities
- Responsible for all deliverables related to statistical content.
- Provide guidance and management to statisticians, programmers, and data managers to ensure high-quality and timely deliverables.
- Advise and influence senior leadership and functional leads on biostatistics strategies and functional issues that have a business impact.
- Oversee the biostatistics function at CROs and manage scopes of work and relationships with external statistical consultants as needed.
- Manage resources, set priorities, and ensure consistency and adherence to standards.
- Collaborate on protocol development, including study design, endpoint selection, and power and sample size assessments.
- Take responsibility for statistical analysis plans, data analysis, and clinical study report content.
- Support Data Monitoring Committee charters and meeting preparation.
- Represent the Company and the Biostatistics function in written and in-person interactions with the FDA, EMA, and other health authorities.
- Support regulatory submissions and interactions, including IND and BLA filings, and support potential partnering requests.
- Serve as an integral member of cross-functional project teams and provide statistical input to clinical development plans, protocols, synopses, investigator brochures, regulatory submissions and responses, scientific publications, and presentations.
- Develop solutions to statistical and data analysis issues for clinical, regulatory, and commercial teams and communicate solutions cross-functionally.
- Contribute to the creation and maintenance of departmental SOPs and standardization efforts, and provide training on statistical topics.
- Maintain current knowledge of developments in statistics, drug development, and regulatory guidance.
- Participate in due diligence evaluations of study designs and clinical trial data for external partnership opportunities as needed.
- Assist with business development activities at key conferences and industry meetings.
- Support scientific and medical meetings, including investigator meetings, advisory boards, DMCs, SABs, and interactions with key opinion leaders.
- Present at industry conferences representing AskBio.
- Participate in vendor evaluation, selection, and management.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Senior
