- Support the healthcare compliance program, including development, enhancement, and roll-out of policies and procedures, risk assessments, audits, monitoring, training and compliance communications
- Support the implementation of required compliance policies and procedures at the affiliates, including engagement of healthcare professionals, grants, and data privacy
- Advise internal clients on the healthcare compliance program and the related processes
- Partner with the business to proactively identify and mitigate areas of potential risk
- Provide compliance training to field and home office personnel, affiliate personnel and external service providers
- Work with external vendors on addressing issues and improving software and other tools used in the Compliance Program
- Analyze data to identify potential risk areas or concerns
- Proactively identify legal risks and work with other internal stakeholders to effectively eliminate or mitigate those risks while concurrently supporting business strategic goals
- Patient Champions, who put patients first and uphold strict ethical standards
- Entrepreneurial Operators, who drive toward practical solutions and have an ownership mindset
- Truth Seekers, who are detailed, rational, and humble problem solvers
- Individuals Who Inspire Excellence in themselves and those around them
- High-quality executors, who execute against goals and milestones with quality, precision, and speed
- 5-8 years of relevant experience in a pharmaceutical or biotech organization
- Must possess strong written and oral communication skills, ability to influence change/be a change agent, and be able to coach, mentor and train others
- Demonstrated skill in critical thinking and acting strategically
- Very strong problem-solving mindset. Serve as thought partner to compliance leadership
- Able to act as a business partner actively engaging stakeholders across the organization in both pre-commercial and commercial environments
- Comfortable with navigating ambiguity and evolving business models
- Knowledge of data privacy laws in the US
- Experience with contract management
- Patient Days, where we are fortunate to hear directly from individuals living with the conditions we are seeking to impact throughout the year and learn how we can improve our efforts
- A culture inspired by our values: put patients first, think independently, be radically transparent, every minute counts, and let the science speak
- An unyielding commitment to always putting patients first. Learn more about how we do this here
- A de-centralized model that enables our program teams to focus on advancing science and helping patients. Our affiliate structure is designed to eliminate bureaucracy and put decision-making power in the hands of those closest to the science
- A place where you own the vision - both for your program and your own career path
- A collaborative, fast-paced, data-driven environment where we inspire ourselves and each other to always perform at the top of our game
- Access to learning and development resources to help you get in the best professional shape of your life
- Robust and market-competitive compensation & benefits package (Base, Performance Bonus, Equity, health, welfare & retirement programs)
- Flexible PTO
- Rapid career advancement for strong performers
- Potential ability to work on multiple BridgeBio Pharma programs across multiple therapeutic areas over time
- Partnerships with leading institutions
- Commitment to Diversity, Equity & Inclusion
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Sr. Manager/Associate Director, Compliance - San Francisco, United States - BridgeBio Pharma, Inc.
Description
About BridgeBio
BridgeBio is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases and cancers with clear genetic drivers.
We bridge the gap between remarkable advancements in genetic science in academic institutions and the delivery of meaningful medicines to patients.
Founded in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
Our focus on scientific excellence and rapid execution aim to translate today's discoveries into tomorrow's medicines. We have U.S. offices in San Francisco, Palo Alto, and Raleigh, with small satellites in other parts of the country. We also have international offices in Montreal, Canada, and Zurich, Switzerland, and are expanding across Europe.To learn more about our story and company culture, visit us at
Who You Are
You have several years of experience building and supporting healthcare compliance programs within life science organizations within the United States.
One of your strengths is the ability to work closely with your business colleagues to develop and maintain processes to help ensure compliant operations and business success.
Responsibilities