Technical Writer • Lead

Who you are

You have extensive experience in medical writing, particularly in the biopharmaceutical industry, and a deep understanding of health authority guidance and requirements for clinical and regulatory documents. Your expertise allows you to navigate complex regulatory landscapes and ensure compliance with public disclosure requirements in applicable regions. You thrive in collaborative environments, working alongside scientists and regulatory professionals to produce high-quality documentation that supports clinical trials and regulatory submissions.

You possess strong leadership skills, having previously established and managed teams focused on medical writing. You understand the nuances of developing clinical documents, including protocols, investigator brochures, and clinical study reports. Your attention to detail ensures that all documents are not only scientifically accurate but also clearly communicate complex information to diverse audiences.

You are adept at mentoring and guiding junior writers, fostering a culture of continuous improvement within your team. You believe in empowering others to excel in their roles and are committed to professional development. Your ability to communicate effectively with cross-functional teams enhances collaboration and drives project success.

Desirable

Experience in rare diseases or specific therapeutic areas relevant to BridgeBio's mission would be a plus. Familiarity with electronic submission processes and tools used in regulatory submissions can further strengthen your candidacy. You are also comfortable working in a fast-paced environment where adaptability and innovative thinking are essential.

What you'll do

In this role, you will lead the Medical Writing group for the Cardiorenal affiliates at BridgeBio, overseeing the development and finalization of clinical and regulatory documents. You will collaborate closely with clinical teams to ensure that all documentation meets regulatory standards and supports the advancement of groundbreaking therapies for patients with unmet needs. Your responsibilities will include developing and maintaining writing standards and templates, ensuring consistency across documents, and implementing best practices in medical writing.

You will also be responsible for reviewing and editing documents produced by your team, providing constructive feedback to enhance clarity and precision. Your leadership will guide the team in managing timelines and deliverables, ensuring that all projects are completed on schedule and to the highest quality standards. You will represent the Medical Writing group in cross-functional meetings, advocating for the importance of clear and compliant documentation in the drug development process.

What we offer

BridgeBio offers a competitive salary range of $260,000 to $300,000 USD, reflecting the importance of this role in our mission to develop life-changing medicines. We provide a supportive and innovative work environment where you can collaborate with some of the most respected minds in the industry. Our hybrid work model allows for flexibility while maintaining strong team connections. You will have the opportunity to contribute to meaningful projects that directly impact patients' lives, making your work both rewarding and impactful.