Sr. Medical Director

Who you are

You are an experienced safety physician with a strong background in clinical development and postmarketing safety strategy. Your expertise allows you to effectively support the safety evaluation and risk management of assigned products, ensuring compliance and safety standards are met. You thrive in collaborative environments, adapting to complex challenges and driving results through teamwork and innovative thinking.

You possess a deep understanding of the biopharma landscape, particularly in rare diseases, and are passionate about developing life-changing medicines for patients with unmet needs. Your ability to engage with key collaborators, both internally and externally, is crucial in advancing the safety and efficacy of the products you oversee. You are someone who defies convention and is excited about pushing boundaries in the industry.

Desirable

Experience in leading safety evaluations and risk management strategies in a clinical setting is highly valued. Familiarity with regulatory requirements and a proven track record of successful product oversight will set you apart. You are comfortable navigating complex problems and are driven by a desire to innovate and improve patient outcomes.

What you'll do

As the Senior Medical Director, you will take charge of the overall safety evaluation and risk management for your assigned products. This includes collaborating with various stakeholders to ensure that safety protocols are adhered to and that any potential risks are effectively managed. You will lead discussions with internal teams and external partners, fostering a culture of safety and compliance throughout the product lifecycle.

Your role will involve analyzing safety data, identifying trends, and making informed decisions that impact product development and patient safety. You will be responsible for developing and implementing safety strategies that align with the company's mission to deliver groundbreaking advancements in rare disease treatment.

In addition to your safety oversight responsibilities, you will play a key role in mentoring and guiding junior team members, sharing your expertise and fostering a collaborative environment. Your leadership will be instrumental in driving the success of the clinical development programs and ensuring that the highest safety standards are maintained.

What we offer

BridgeBio offers a competitive salary range of $325,000 to $370,000 USD, reflecting the importance of this role within our organization. We are committed to fostering a supportive and innovative work environment where you can thrive and make a meaningful impact in the biopharma industry. Join us in our mission to redefine the future of medicine and improve the lives of patients with rare diseases.