With more than 20 years of experience in the pharmaceutical industry, I am Director, Operations at MMS – a global, leading clinical research organization. On a daily basis, I work with the global team members to ensure outstanding services that meet regulatory requirements and high-quality standards.Prior to my tenure at MMS, I spent over 15 years at Pfizer where I led the regulatory operations team supporting global regulatory submissions across many therapeutic areas and indications as Associate Director.As a leader, I am a focused on encouraging the skills and strength of each individual that contribute to our exceptional high-quality services.
Listed skills include Regulatory Submissions, Pharmaceutical Industry, Clinical Trials, Regulatory Affairs, and 17 others.