Director, Regulatory Counsel

Edwards Lifesciences

San Francisco (CA)

On-site

USD 174,000 - 246,000

Full time

19 hours ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Edwards Lifesciences seeks a Director, Regulatory Counsel to provide practical, timely legal guidance across the company’s Healthcare Regulatory activities. The role focuses on reviewing advertising and promotional materials, advising on fraud and abuse issues, and supporting strategic clinical and commercial contracts.

The successful candidate will partner with Marketing, Regulatory Affairs, Compliance and other functions, ensuring compliance with FDA-regulated processes and 510(k)/PMA pathways

Qualifications

  • Juris Doctor from ABA-accredited law school.
  • 8+ years of legal experience in law firm or in-house.
  • Strong written and verbal communication with business audiences.
  • Ability to work under pressure and prioritize conflicting demands.

Responsibilities

  • Provide legal guidance to Edwards across business units and corporate functions.
  • Review and advise on advertising and promotional materials for regulatory compliance.
  • Advise on fraud and abuse issues and clinical contracts.
  • Negotiate and advise on strategic clinical and commercial contracts.
  • Develop and harmonize standard processes and templates for the Healthcare Regulatory team.
  • Deliver legal education on regulatory pathways and FDA processes.
  • Monitor healthcare regulatory developments and build area expertise.

Skills

Legal communication
Problem solving
Strategic thinking
Team collaboration

Education

Juris Doctor (ABA-accredited)

Job description

Make a meaningful difference to patients around the world! Our Legal team works to protect our patients, team members, and innovations with the utmost diligence and care. You’ll have the opportunity to work with a dedicated team and build lasting partnerships with stakeholders across our global organization. Your legal knowledge and contributions will help us ensure that we are supporting the needs and interests of the patients we serve.

The Director, Regulatory Counsel reports to the Vice President, Regulatory Counsel and will be responsible for timely review and approval of advertising and promotion materials, provision of advice and counsel with respect to fraud and abuse issues, analysis of clinical contracts, assistance with state licensing, support for sales contracting, and other legal regulatory duties as needed. The Director, Regulatory Counsel will closely partner with Marketing, Clinical Affairs, Regulatory Affairs, Compliance and other functional groups within Edwards, and will require a thorough understanding of each of Edwards’ business units and the products they manufacture and sell. The successful candidate will have a unique opportunity to help Edwards achieve its business objectives by providing practical, timely and effective legal counsel, while minimizing potential legal risks (and having fun doing it as part of a great team).

Work Schedule:

Given the collaborative and complex nature of this work, this role is in person full time in Irvine, California. Relocation will be provided for qualified candidates.

How you’ll make an impact:

Providing legal guidance to Edwards, including working closely with each of the business units and Corporate functions. Reviewing and advising on a variety of advertising and promotional pieces, including print and digital ads, social media campaigns, speaker presentations, and other materials to determine compliance with applicable regulations and policies and assess corporate risk.

  • Providing advice and counsel with respect to fraud and abuse issues.
  • Reviewing and advising on clinical contracts and a variety of legal issues related to clinical trials.
  • Reviewing, negotiating, and advising on strategic clinical and commercial contracts across business units
  • Developing and harmonizing standard processes and templates; creating, improving, and institutionalizing knowledge base for the Healthcare Regulatory team.
  • Developing and delivering legal education to business colleagues in specific areas (e.g., regulatory approval processes, pathways to market (510(k), PMA, etc.), requirements for FDA-regulated clinical investigations, etc.).
  • Monitoring legal developments applicable to the Healthcare Regulatory and medical device spaces and developing expertise in strategic focus areas.
  • Other duties and responsibilities as assigned.
What you'll need (Required):
  • Juris Doctor from ABA-accredited law school with 8 years of legal experience at a law firm or in-house legal department.
  • Strong written and verbal communication and interpersonal skills, including the ability to convey nuanced legal concepts/issues clearly and succinctly to legal and business decision makers.
  • Excellent independent problem-solving, critical thinking, and investigative skills
  • Strategic thinking, proactive mindset, and excellent problem-solving abilities.
  • Ability to be a team player and a trusted business partner.
  • Ability to work under pressure and prioritize projects and tasks appropriately.
What else we look for (Preferred):
  • Background in life sciences, MedTech, pharmaceuticals, or related healthcare industry experience preferred.
  • Experience in advertising and promotion in the medical device or pharmaceutical industry or at a healthcare system.
  • Experience providing advice and counsel with respect to fraud and abuse issues in the medical device or pharmaceutical industry.
  • Prior-in house experience in life sciences, MedTech, pharmaceuticals, or related healthcare industry preferred.

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

For California (CA), the base pay range for this position is $174,000 to $246,000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Director, Regulatory Counsel
Director, Regulatory Counsel

Edwards Lifesciences • Washington

On-site
USD 174,000 - 246,000
Competitive salaries
Performance-based incentives
Benefits programs
Director, Regulatory Counsel
Director, Regulatory Counsel

Edwards Lifesciences • Irvine (CA)

On-site
USD 174,000 - 246,000
Competitive salary
Incentives
Benefits program
Senior Manager of US Healthcare Regional Compliance
Senior Manager of US Healthcare Regional Compliance

Edwards Lifesciences Gruppe • California (MO)

Hybrid
USD 121,000 - 170,000
Senior Director, Global Compliance Policy and Program
Senior Director, Global Compliance Policy and Program

YourGeneralCounsel • Irvine (CA)

Hybrid
USD 173,000 - 245,000
Analyst, Clinical Contracts and Budgets
Analyst, Clinical Contracts and Budgets

Edwards Lifesciences Gruppe • Irvine (CA)

On-site
USD 68,000 - 96,000
Senior Director, Global Compliance Policy and Program
Senior Director, Global Compliance Policy and Program

Edwards Lifesciences • Irvine (CA)

Hybrid
USD 173,000 - 245,000
Senior Director, Global Compliance Policy and Program
Senior Director, Global Compliance Policy and Program

Edwards Lifesciences Gruppe • California

Hybrid
USD 173,000 - 245,000
Competitive salaries and incentives
Comprehensive benefits
Senior Manager of US Healthcare Regional Compliance
Senior Manager of US Healthcare Regional Compliance

Edwards • Irvine (CA)

Hybrid
USD 121,000 - 170,000
Senior Director, Clinical Affairs
Senior Director, Clinical Affairs

Edwards Lifesciences • Irvine (CA)

On-site
USD 209,000 - 296,000
Senior Director, Clinical Affairs
Senior Director, Clinical Affairs

Edwards Lifesciences Gruppe • Redhill (MD)

On-site
USD 209,000 - 296,000