Job Description
Join BioNova Therapeutics, a leader in innovative drug discovery, as we pioneer next-generation therapeutics for unmet medical needs. We seek a passionate Senior Research Scientist to drive our cutting-edge pharmaceutical research initiatives. In this pivotal role, you'll collaborate with multidisciplinary teams to advance drug candidates from conception to clinical trials, leveraging state-of-the-art facilities and a culture of scientific excellence.
Our Cambridge campus offers unparalleled resources for translational research, including a fully equipped GMP lab and partnerships with MIT/Harvard. Enjoy competitive benefits, flexible work arrangements, and opportunities to present at international conferences. Help us shape the future of medicine while advancing your career in one of biotech's most dynamic environments.
Responsibilities
- Lead design and execution of complex in vitro/in vivo pharmacology studies for novel drug candidates
- Develop and optimize biochemical/cellular assays to evaluate compound efficacy and safety
- Analyze and interpret large-scale biological data using advanced statistical methods
- Mentor junior scientists and oversee lab operations ensuring compliance with FDA/ICH guidelines
- Collaborate with regulatory affairs team to prepare IND submissions and clinical trial documentation
- Present research findings at internal/external forums and publish high-impact papers
Qualifications
- PhD in Pharmacology, Molecular Biology, or related life science field with 5+ years industry experience
- Proven expertise in drug discovery pipelines from target identification to preclinical development
- Advanced proficiency in cell-based assays, high-throughput screening, and molecular techniques
- Strong analytical skills with experience in bioinformatics and data visualization tools
- Demonstrated success in leading cross-functional projects and managing research budgets
- Excellent written/verbal communication skills with publication record in peer-reviewed journals
- Knowledge of GMP/GLP regulations and clinical trial design principles