Associate Director/Director, IT Business Systems R&D

Who you are

You have a strong background in IT business systems, particularly within the pharmaceutical or biotech industries. With at least 5 years of experience, you have a proven track record of leading system implementations and migrations, particularly in pharmacovigilance. Your expertise in Veeva Vault Safety and related systems is complemented by a deep understanding of compliance and data integrity requirements in the industry. You thrive in collaborative environments and are adept at aligning technology with business processes to drive operational efficiency.

You are a strategic thinker who can define and execute roadmaps that support both commercial and clinical functions. Your ability to communicate complex technical concepts to non-technical stakeholders is one of your key strengths. You are passionate about leveraging technology to improve patient safety and outcomes, and you are excited about the opportunity to work with a team that is dedicated to innovation in rare disease treatment.

Desirable

Experience with other Veeva vaults such as Quality, RIM, and eTMF is a plus. Familiarity with data migration processes and tools will enhance your ability to succeed in this role. You are comfortable working in a fast-paced environment and are eager to take on challenges that push the boundaries of traditional biopharma practices.

What you'll do

In this role, you will lead the design and implementation of BridgeBio's global pharmacovigilance systems landscape. You will oversee the migration of safety data and processes from Argus to Veeva Vault Safety, ensuring that all data is handled with the utmost integrity and compliance. Your leadership will be critical in defining the Safety Systems roadmap, aligning technology with business needs across the organization.

You will collaborate closely with cross-functional teams, including clinical, commercial, and IT departments, to ensure that the systems you implement meet the diverse needs of the organization. Your role will involve continuous improvement of existing systems and processes, identifying opportunities for optimization and innovation.

You will also be responsible for training and supporting users of the pharmacovigilance systems, ensuring that they are equipped to utilize the tools effectively. Your insights will help shape the future of BridgeBio's approach to safety and compliance, making a tangible impact on the lives of patients with unmet needs.

What we offer

BridgeBio offers a competitive salary range of $216,530—$245,000 USD, reflecting the importance of this role within our organization. We provide a supportive and collaborative work environment where innovation is encouraged, and your contributions will be valued. You will have the opportunity to work alongside some of the most respected minds in the industry, contributing to groundbreaking advancements in rare disease treatment.

We believe in empowering our employees to achieve their best work and offer opportunities for professional growth and development. Join us in our mission to redefine the future of biopharma and make a difference in the lives of patients around the world.