
Organized Principal Scientist skilled in designing and executing 5 preclinical and 1 clinical phase research projects per year. Superb written and verbal communication skills. Seasoned at preparing reports, publications and oral presentations for small or large groups. Successfully secured and worked on completing milestones for 3 separate collaborations with industry partners. Oversaw the transition from preclinical to clinical drug use in a Phase 0 and Phase I/II. Synthesized all drug formulations that went into preclinical and Phase 0 clinical work. Successfully optimized and transferred technology for the drug production to the selected CDMO for the primary drug product. Designed and developed drug formulations for the other pipeline projects as well as carried out the synthesis and characterization of all drug material. Well versed now in Chemistry, Manufacturing and Controls (CMC), Quality and Manufacturing on top of laboratory research and development, intellectual design and project/team management.
Analytical mindset
Product Development
Cultural Awareness
Public speaking abilities
Project management experience
Strong leadership abilities
Critical thinking abilities
Subject matter expertise
Collaborative mindset
Interdisciplinary Collaboration
Process Development
Cross-functional Team Coordination
Results-driven focus
Lab Safety Protocols
Clinical Trial Oversight
Technology transfer knowledge
Publication record
Innovative problem-solving
Technical Writing Expertise
Expertise in research
Continuous Improvement Mindset
Laboratory techniques
Quantitative skills
Safety processes and procedures
Research and experiments
Research and publication
Experimental design
Results Analysis