Mr. Paul G Dionne

biography

Paul reaches out to busy senior leaders, vice presidents and CEOs that don't have the time or resources to screen and interview a slew of candidates. His team aims to provide three excellent candidates in less than 21 business days for your Regulatory, Quality, Clinical or Medical position.

Here are some great passive candidates I am representing:

**** Board certified DO who is a Medical Director for Global Safety. For our previous client, he wrote all the phase 3 safety sections and phase 2 CSR's, setting up and running their safety and pharmacovigilance operations, while keeping operations lean until the company was sold. Before that, he spent 9 years at Amgen where he started as individual contributor and ended overseeing 150 people in therapeutic areas including Oncology, Hematology, Nephrology, Rheumatology, Neurology, Cardiovascular and Bone. For both companies he helped them build in-house safety -data databases using cloud based systems. He holds a DO [licensed in CA and AZ] and a MS in Public Health. [

**** VP Medical Affairs with 10 years of oncology (including cancer stem cells) experience including time Bayer and Sanofi . At Sanovi he was the medical lead when phase 3 data was better than expected. In 8 weeks he led a $150m launch for which his team won the Pinnacle Award. He also created and implemented medical strategy for a growing biotech firm and successfully built and led Medical Affairs teams in multiple therapeutic areas. He holds a MD. [active 5yrs now inactive -open to relocation] [ready to relocate nationally]

**** VP of Clinical Development providing cross functional leadership for an oncology drug through its successful Phase III study. She served as the clinical representative on a team that closed a $1B exclusive with a major pharmaceutical company. Prior to that she oversaw a development portfolio of 5 drugs concurrently (preclinical to phase 3) She is a licensed MD, a PhD in Neurology and is DEA registered. [ Immunotherapy; Neurology; Autoimmune ] [west coast positions only]

**** National Director of Clinical Research Operations with 11 years of clinical trials experience and 8 years of leadership experience in infectious, metabolic & cardiovascular diseases. His current position is with a clinical trials site overseeing a staff of 50. Fluent in Spanish, he has setup and overseen sites in Mexico and Argentina serving as their medical liaison in the event of a SAE. He has experience working with US, EU, South American, and South East Asian regulatory agencies. He serves on a prestigious FDA Advisory committee and is a boarded MD with a PhD in immunology. [willing to relocate self globally]

**** Sr. Director of Device Packaging and Engineering. Focused on site equipment capacity and design for scalability. Oversees team of 55 people spread across the world. He is a certified packaging professional (lifetime achievement) BS in Industrial Technology and Packaging. [will to relocate globally]