• Provide strategic leadership for infrastructure, managed services, and digital platform capabilities supporting custom scientific and business applications. • Partner with product owners, engineering teams, and customer programs to identify new service opportunities and translate mission needs into actionable technology solutions. • Lead, mentor, and develop technical teams; set performance expectations, guide career growth, and cultivate a culture of accountability, innovation, and continuous improvement. • Drive the implementation of automation, infrastructure‑as‑code, and modern software delivery approaches to improve scalability, reliability, and efficiency. • Communicate complex technical concepts through clear visualizations, briefs, and presentations for both technical and executive audiences. • Oversee cross‑functional collaboration across engineering, security, architecture, and operations to deliver integrated and resilient solutions. • Contribute to proposal development and technical solutioning to support new business opportunities and expand customer mission impact. • Provide thought leadership on infrastructure technologies, digital modernization, and emerging industry trends that influence long‑term strategy.

Role Description A well-established, secure and commercially active biopharma is expanding its US biostatistics team. This is a specialized role focused on biomarker statistical analysis across an oncology portfolio, within a fully in-house function. - Responsibility for all Biomarker data for the company Oncology portfolio - Develop and review biomarker analysis plans and statistical sections of study protocols - Integrate biomarker data with clinical outcomes to support translational and regulatory objectives - Collaborate with clinical development, translational science, and biometrics teams - Support regulatory interactions and contribute to clinical study reports - Conduct ad hoc biomarker statistical analysis as required Qualifications - PhD in Biostatistics or Statistics; Masters with supplementary experience considered - Extensive oncology experience with a focus on biomarker or translational statistics - Demonstrable experience working directly for a sponsor company - Proficiency in SAS and/or R - Strong understanding of biomarker endpoints and translational study designs - East Coast based only Requirements - Compensation DOE - $180,000 - $240,000 base salary + benefits

Role Description A well-established, secure and commercially active biopharma is building out its US statistical programming team. This is a senior leadership role that will oversee the build-out of a fully in-house function. - Lead the statistical programming function for the oncology portfolio - Build and develop the new US statistical programming team - Define programming strategy, standards, and processes - Oversee in-house development and validation of SDTM, ADaM datasets, and TFLs - Support regulatory interactions, including IND, NDA/BLA submissions - Collaborate with Biostatistics, Clinical Data Management, and Regulatory on submission readiness Qualifications - Bachelor's or Master's degree in a relevant discipline - Extensive SAS programming experience within pharma or biopharma; oncology background required - Demonstrable experience working directly for a sponsor company - Strong knowledge of CDISC standards (SDTM, ADaM) and FDA/EMA submission requirements - Proven leadership of a programming team or function - East Coast based only Requirements - Compensation DOE - $250,000 - $300,000 base salary + benefits

Role Description A well-established, secure and commercially active biopharma is building out its US biostatistics team. This is a senior leadership role that will oversee the build-out of a fully in-house function. - Lead the biostatistics function for the oncology portfolio - Build and develop the new US biostatistics team - Drive statistical strategy across early phase through to registrational trials - Author and review Statistical Analysis Plans (SAPs) and statistical sections of clinical protocols - Oversee production of Tables, Figures, and Listings (TFLs) and clinical study reports - Represent biostatistics cross-functionally and in interactions with regulatory authorities - Support regulatory interactions, including IND, NDA/BLA submissions Qualifications - PhD in Biostatistics or Statistics; Masters with supplementary experience considered - Extensive oncology experience - Demonstrable experience working directly for a sponsor company - Proven leadership within a biostatistics function - Track record of supporting or leading regulatory submissions - Strong communication skills across statistical and non-statistical audiences - East Coast based only Requirements - Compensation DOE - $220,000 - $320,000 base salary + benefits