Medical Director

M.D. degree with completion of an ACGME accredited residency 3+ years of experience in academics or industry; candidates without industry experience should preferably have completed a fellowship Experience in clinical trial design, execution, and medical monitoring Strong clinical judgment, scientific rigor, and regulatory knowledge Ability to work independently and thrive in a fast-paced, matrixed environment Ability to manage multiple projects simultaneously and prioritize effectively in a fast-paced environment Strong analytical, problem-solving, and decision-making skills Excellent communication and interpersonal skills High ethical standards and impeccable integrity Exercise sound judgment in managing complex, confidential, and regulated information

Lead the design, execution, and oversight of clinical trials Provide leadership to study teams Serve as a Medical Monitor for clinical trials Analyze, interpret, and report clinical data Ensure timely and accurate completion of trial-related documents Build and maintain relationships with investigative sites, clinical consultants, and key opinion leaders Collaborate with the internal safety team to analyze and report safety data Apply medical expertise and hands-on clinical experience to ensure the relevance and rigor of the development program Collaborate with cross-functional teams to optimize product development Maintain scientific and clinical expertise in the relevant disease-specific area