Melinda Whiteside

Melinda Whiteside

Senior Director and Head of Clinical Operations at Armo Biosciences, Inc.

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Location:
575 CHESAPEAKE DRIVE, Redwood City, California, United States
HQ Phone:
(408) 396-1416

General Information

Experience

Project Manager Responsible for Sponsor Management  - Phoenix International Life Science

Clinical Research Consultant  - Genentech , Inc.

Senior Director, Clinical Operations and Project Management  - ACT Biotech Inc

Education

B.S.  - Biology , McGill University

Recent News  

Melinda Whiteside
Senior Director and Head of Clinical Operations Melinda Whiteside, BS has 21 years of experience in the biotech industry. Prior to ARMO, she held positions of increasing responsibility within clinical development at Genentech, Titan Pharmaceuticals and Roche. Most recently, Melinda was Senior Director of Clinical Operations and Project Management at Accelerate Cancer Therapeutics, Inc. Melinda has been responsible for the clinical operations management and execution of Phase 1, 2 and 3 stage clinical studies in cancer and in cardiovascular, metabolic and neurologic diseases. Melinda received a B.S. in Biology from McGill University in Montreal, Canada.

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Melinda Whiteside, Senior Director and Head of Clinical Operations
Melinda Whiteside, BS has 21 years of experience in the biotech industry. Prior to ARMO, she held positions of increasing responsibility within clinical development at Genentech, Titan Pharmaceuticals and Roche. Most recently, Melinda was Senior Director of Clinical Operations and Project Management at Accelerate Cancer Therapeutics, Inc. Melinda has been responsible for the clinical operations management and execution of Phase 1, 2 and 3 stage clinical studies in cancer and in cardiovascular, metabolic and neurologic diseases. Melinda received a B.S. in Biology from McGill University in Montreal, Canada.

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Melinda Whiteside, Director, Clinical Operations
Melinda Whiteside has 15 years of clinical research and project management experience and has joined ACT as Director of Clinical Operations. Prior to joining ACT, Melinda was Director of Clinical Operations at Titan Pharmaceuticals where she was responsible for operational strategic development, management and execution of clinical programs in Phase I-III clinical trials in North America, South America, Europe, Asia, and South Africa in the therapeutic areas of oncology, cardiovascular and central nervous system. She worked as Global Clinical Operations Manager at Roche Global Development managing and leading international teams conducting global trials for products such as Tamiflu® , Xenical® and Tasmar®. Melinda started off her career at Phoenix International Life Science (now MDS), a contract research organization as a Project Manager responsible for sponsor management and overall management of clinical trials and as a Clinical Research Associate responsible for monitoring clinical trials.

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