A biotechnology consulting firm is seeking a Regulatory Affairs Consultant to support projects with about 10-20 hours of work per week. This remote position requires expertise in regulatory strategy development, especially in relation to in-silico modeling. Candidates must possess an advanced degree and a minimum of 10 years of experience in global regulatory applications for pharmaceutical products. Responsibilities include leading regulatory submissions, engaging with the FDA, and providing guidance on in-silico strategies. #J-18808-Ljbffr