News Releases

News Releases

Synteract Bolsters Regulatory and Medical Writing Expertise

Taking a product from concept to cure is no easy feat. Most often, it’s a tough, expensive, and lengthy process. One difficult area to navigate concerns the regulatory requirements in every country around the world. Our regulatory experts have the proven experience and expertise to help bring products to life.

Angela StokesThat's why we're very excited to add another strong member to our proven regulatory team. Angela Stokes has joined our regulatory team as the vice president of regulatory affairs. She's got an impressive background; most recently she led the regulatory affairs team at Syneos Health. She brings 30 years of experience working across a variety of regulatory documentation preparation, submission, and consulting roles in both start-up and large pharmaceutical companies and CROs worldwide. Her experience spans the U.S., EU, China, Japan, and Australia, as well as other countries.

As the former president and fellow of the Organisation for Professionals in Regulatory Affairs (TOPRA) and as a fellow of the Royal Society of Chemistry, she has leadership skills supported by her extensive expertise in chemistry, math, pharmacology, and toxicology.

Angela has currently been nominated for a 2020 TOPRA Regulatory Affairs Excellence Award in the Inspiration category, reflecting her career-long journey to inspire the regulatory affairs community, encouraging action and innovative outcomes.

Molly RodriguezWe're just as excited to add Molly Rodriguez to our medical writing team as global head. With more than 27 years of experience in CRO, government, and academic backgrounds, Molly is an accomplished researcher, medical writer, and leader with experience in global team management, regulatory affairs, clinical research, and public health. 

Molly has a bachelor's degree in technical writing and biological sciences, as well as a master's degree in public health (MPH). Her therapeutic area experience includes dermatology, oncology, rare and orphan diseases, neuroscience, endocrinology, women's health, devices, pediatrics, anesthesia, infectious disease (acute respiratory illness, HIV, vector-born infection, and bioterrorism threats including anthrax and smallpox), as well as considerable experience in PK/PD drug interaction studies.

Angela and Molly's proven experience will contribute to our "Dossier Submission: Ready, Set, Submit" service offering to help clients manage full marketing authorization application submissions and bring even more clout to our regulatory and medical writing teams as we continue our mission to bring clinical trials to life.

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