Medical Director • Senior

Who you are

You have a strong background in drug safety and risk management, with a proven track record of overseeing safety profiles from clinical development to post-approval surveillance. Your experience includes managing relationships with CROs and other partners to ensure comprehensive safety data collection and analysis. You are adept at leading safety management committees and have a deep understanding of regulatory requirements and industry standards. Your ability to communicate effectively with cross-functional teams and external collaborators is essential for success in this role. You thrive in a fast-paced environment and are motivated by the challenge of developing life-changing medicines for patients with unmet needs. You are someone who defies convention and is excited about pushing the boundaries of biopharma innovation.

Desirable

Experience in a commercial-stage biopharmaceutical company is a plus, as is familiarity with rare diseases and innovative treatment approaches. A strong network within the industry can enhance your effectiveness in this role, and any additional certifications in drug safety or pharmacovigilance will be beneficial.

What you'll do

As the Senior Medical Director of Drug Safety, you will be responsible for the overall safety strategy of assigned products, ensuring that all aspects of safety are managed effectively. You will chair the Safety Management Committee for designated products, leading discussions on risk assessment and mitigation strategies. Your role will involve engaging with internal teams and external partners to gather and analyze safety data, making informed decisions that impact product development and patient safety. You will oversee the preparation of safety reports and ensure compliance with regulatory requirements, contributing to the overall success of the company's drug development programs. Collaboration with clinical development teams will be crucial as you work to integrate safety considerations into all phases of product development. You will also mentor junior staff and contribute to the development of best practices within the organization.

What we offer

BridgeBio offers a competitive salary range of $310,000 to $340,000 USD, reflecting the importance of this role within our organization. We provide a supportive and innovative work environment where you can collaborate with some of the most respected minds in the industry. Our commitment to groundbreaking advancements in rare disease treatment means that your work will have a direct impact on the lives of patients. We encourage you to apply even if your experience doesn't match every requirement, as we value diverse perspectives and backgrounds in our team.