BridgeBio Pharma, Inc.

Program Management Sr. Manager

BridgeBio Pharma, Inc.$180K — $195K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • M.S. or B.S. in chemistry, chemical engineering, or equivalent preferred with a solid understanding of drug development science.
  • Minimum of 10 years of project management experience in the biotech/pharma industry.
  • Proven ability to deliver in a fast-paced and dynamic environment with flexibility and resourcefulness.
  • Strong planning and tracking skills with a focus on managing multiple projects efficiently.
  • Capability to work strategically and independently with diverse internal and external teams.

Responsibilities

  • Organize and coordinate CMC/QA team activities, managing team meetings and tracking action items.
  • Collaborate with multiple CDMOs to ensure alignment of manufacturing activities with CMC timelines.
  • Ensure adherence to team goals, coordinating the drafting of regulatory filing sections and conducting document quality control.
  • Engage in long-range and budgetary planning while collaborating with Legal and Finance on vendor contracts.
  • Manage concurrent responsibilities and deliverables effectively.

Benefits

  • Market-leading compensation package
  • 401(k) with employer matching contribution
  • Employee Stock Purchase Program (ESPP)
  • 100% employer-paid medical, dental, and vision premiums for employees and dependents
  • Flexible
  • take-what-you-need
  • paid time off and company-paid holidays
Full Job Description
What You'll Do

The Senior Manager, Project Management will report to the Director, Program Management, and support the CMC team to ensure that cross-functional planning is incorporated in department activities, identified risks, mitigation plans are established to address the risks, and resource needs are identified and addressed proactively. The successful candidate must communicate effectively with internal stakeholders and external partners.

Responsibilities
• Organize and coordinate CMC/QA team activities and deliverables; manage weekly team meetings; prepare agendas and keep track of action items
• Interface and manage multiple CDMOs to drive manufacturing activities in alignment with CMC timelines and clinical and commercial supply needs
• Responsible for ensuring adherence to agreed-upon team goals and deliverables. Coordinate drafting of certain sections of regulatory filing and cross-functional reviews. Organize document QC processes to ensure accuracy of content
• Contribute to long-range planning and budgetary planning. Work with Legal and Finance departments to drive and manage vendor contracts and purchase orders
• Effectively manage multiple responsibilities and deliverables concurrently

Where You'll Work

This is a hybrid role and requires in-office collaboration 2-3x per week in our San Francisco office.

Who You Are

Historically the "Experience, Education, & Skills Requirement" section

(5-7 bullets max)
  • M.S. or B.S. in chemistry, chemical engineering or equivalent preferred. Demonstrated understanding of science behind drug development is required
  • A minimum of 10 years of biotech/pharma industry project management
  • Track record of delivering in a fast-paced, innovative, dynamic environment while remaining flexible, proactive, resourceful, and efficient
  • Expert planning and tracking skills, able to see the big picture, well-organized, focused on results, capable of managing multiple projects, excellent time management concerning priorities and self-management
  • Ability to work strategically and independently with internal and external groups on multiple projects
  • This position may require some (


At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states.

Salary

$180,000-$195,000 USD

As a global company, our comprehensive benefits may vary based on location. We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.

For Full-Time U.S Based Roles:

Financial & Rewards
  • Market-leading compensation
  • 401(k) with employer match
  • Employee Stock Purchase Program (ESPP)
  • Pre-tax commuter benefits (transit and parking)
  • Referral bonus for hired candidates
  • Subsidized lunch and parking on in-office days

Health & Well-Being
  • 100% employer-paid medical, dental, and vision premiums for you and your dependents
  • Health Savings Account (HSA) with annual employer contributions, plus Flexible Spending Accounts (FSA)
  • Fertility & family-forming benefits
  • Expanded mental health support (therapy and coaching resources)
  • Hybrid work model with flexibility
  • Flexible, "take-what-you-need" paid time off and company-paid holidays
  • Comprehensive paid medical and parental leave to care for yourself and your family

Skill Development & Career Paths:
  • People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility
  • We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching
  • We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities

About BridgeBio Pharma, Inc.

BridgeBio Pharma, Inc. is a biotechnology company that focuses on developing medicines for genetic diseases. The company's pipeline includes over 20 development programs, including treatments for diseases such as achondroplasia, adrenoleukodystrophy, and cystinosis. BridgeBio Pharma, Inc. also has a subsidiary, Eidos Therapeutics, which focuses on developing treatments for transthyretin amyloidosis. The company was founded in 2015 and is headquartered in Palo Alto, California.
Learn more about BridgeBio Pharma, Inc.
Size
576 employees
Market Cap
$1 billion
Industry
Net Income
-$448.7 million
Founded
2014
Revenue
$8.2 million
NASDAQ

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