Future Tech Jobs
Future Tech Jobs
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...
The role involves leading statistical strategy and execution across clinical development programs, including study design, data analysis, and regulatory submissions. The individual will provide expert statistical input, manage internal or outsourced programming teams, and represent biostatistics in interactions with global regulatory agencies. Emphasis is placed on innovation, cross-functional collaboration, and delivery of high-quality statistical outputs for clinical trials and submissions.
This role leads global regulatory strategy for high-profile cell therapy programs, shaping end-to-end development from discovery to approval. The individual will direct complex health authority engagements, define target product labeling, and drive regulatory innovation to accelerate patient access. They will also lead and develop regulatory teams, influence policy, and ensure strategic alignment across cross-functional and international stakeholders.
Lead CMC strategy and execution for small molecule drug development from Phase 2 through commercialization, managing cross-functional teams and global regulatory filings. Oversee tech transfer, process scale-up, and lifecycle planning while ensuring compliance with US, EU, and international standards. Interface with senior leaders and health authorities to drive successful product launches and post-approval activities.
This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regulatory leads, partnering on global strategies, and representing the function in senior interactions and health authority meetings.
This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology R&D. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive strategic alliances and complex collaborations.
This role involves leading the development and implementation of biomarker strategies for neuroscience drug programs, integrating translational data science, and guiding cross-functional teams through clinical and regulatory processes. The Director will oversee biomarker components in clinical studies, mentor specialists, and ensure regulatory compliance while advancing precision medicine in a collaborative, innovation-driven environment.
The Senior Regulatory Associate at Pfizer is responsible for managing regulatory activities for assigned products and markets, including new registrations, MA variations, and renewals. They will work closely with cross-functional teams, national regulatory authorities, and above-country hubs to ensure compliance and support clinical development activities.
In this role, you will develop and lead complex projects, manage economic research studies for clinical trials, and formulate research plans to enhance the value of Pfizer's medicines. You will collaborate with sales teams and utilize health economic models to maximize sales and improve customer interactions.
As a DMPK Lead, you will drive the DMPK strategy for drug discovery projects, integrating quantitative pharmacology and AI-first approaches. You will design and implement DMPK strategies, optimize the use of datasets, and collaborate with interdisciplinary teams to advance drug design and development.
This role involves leading quality strategy across the full product lifecycle in a pharmaceutical development environment. You'll drive design reviews, risk management, and quality system implementation while working closely with project teams and stakeholders. The position emphasizes proactive quality integration rather than post-hoc review, with a focus on influencing technical decisions and ensuring compliance through GMP and ISO standards.
