
Pharm.D professional with 6+ years of experience in Medical Affairs and Scientific Services within the pharmaceutical industry. Expertise in scientific documentation review, prescribing information support, compliant promotional material evaluation, and effective cross-functional coordination with regulatory and quality teams. Actively pursuing a Regulatory Affairs role to leverage strong scientific and compliance knowledge in regulatory submissions, labeling, and product launches. Highly-motivated employee with a desire to take on new challenges. Strong work ethic, adaptability, and exceptional interpersonal skills. Adept at working effectively unsupervised and quickly mastering new skills.