Jeanette (Jenny) G.
About Jeanette (Jenny) G.
Jeanette (Jenny) G. serves as the Director of Clinical Operations, overseeing the strategic planning and implementation of clinical development programs. With extensive experience in managing clinical trials across various therapeutic areas, she has held multiple roles in prominent organizations within the pharmaceutical industry.
Current Role at Nektar Therapeutics
Jeanette G. serves as the Director of Clinical Operations at Nektar Therapeutics, a position she has held since 2021. In this role, she is responsible for the strategic planning and implementation of clinical development programs. Her responsibilities include scenario planning, protocol review, and managing Study Management Team (SMT) meetings. She also oversees database lock management and contributes to the forecasting of timelines, resource estimation, and budget planning for clinical development programs.
Previous Experience at Nektar Therapeutics
Prior to her current position, Jeanette G. worked at Nektar Therapeutics as the Associate Director of Clinical Operations from 2019 to 2020. During her tenure, she gained valuable experience in clinical operations, further developing her expertise in managing clinical trials and supporting regulatory inspections.
Education and Expertise
Jeanette G. holds a Bachelor of Arts (BA) in Microbiology from Sonoma State University, where she studied from 2000 to 2004. She later earned a Master of Science (M.S.) degree from San Jose State University, completing her studies from 2012 to 2015. Her educational background has equipped her with a strong foundation in the biological sciences, which supports her extensive experience in clinical research and operations.
Clinical Research Experience
Jeanette G. has extensive experience in managing clinical trials across various therapeutic areas, including AL Amyloidosis, Neuroscience, Dermatology, Oncology, and Ophthalmology. Her career includes roles at several organizations, such as ProTrials Research, Janssen, and Prothena Corporation plc. She has been involved in risk management, issue escalation management, and the preparation and support of mock and FDA inspections throughout her career.
Professional Contributions
In her roles, Jeanette G. has authored and reviewed Standard Operating Procedures (SOPs) and has played a significant role in clinical trial management. Her responsibilities have included managing clinical trial teams and ensuring compliance with regulatory requirements. She has developed skills in scenario planning and protocol review, contributing to the overall success of clinical development programs.