Dr. Stuart Grant has been promoted to associate director of regulatory affairs and medical writing at ClinTec International. Dr. Grant joined the company in 2010 as senior manager of medical writing and regulatory affairs with more than 9 years industry experience. Previously he was a regulatory affairs consultant at a global CRO, where he was responsible for managing Phase I–IV regulatory submissions and study start-up activities. His experience covers several therapeutic and research areas including cardiovascular, respiratory, psychiatry, pharmacokinetics and medical devices.
Dr. Grant stated, “I’m delighted to be given this opportunity within ClinTec. The company is continuing to expand into new geographical regions and pharmaceutical sectors, which inevitably require us to adapt our processes to satisfy the various regulatory requirements. I’m excited to be heading these departments and look forward to the challenges and opportunities that our continuing growth will bring in these areas.”