ClinTec makes a promotion
Stuart Grant takes newly created role of associate director of regulatory affairs
Based at ClinTec’s headquarters in Glasgow, Scotland, Grant joined ClinTec in 2010 as a senior manager of Medical Writing and Regulatory Affairs with more than nine years of industry experience.
Since joining ClinTec, Grant has initiated several Regulatory and Medical Writing processes. His work in Regulatory Affairs has spanned clinical trial application oversight, orphan drug applications, medical device regulations, therapeutic area consulting and clinical development planning. In the Medical Writing department, he has been responsible for developing and finalising protocols, reviewing documents written by his team and developing the SOP suite.
