Senior Program Director, Commercial Regulatory Affairs

Joulé

South San Francisco, CA

JOB DETAILS
SALARY
$120–$122.40 Per Hour
SKILLS
Advertising, Biology, Biotech and Pharmaceutical, Business Administration, Change Management, Clinical Practices/Protocols, Communication Skills, Cross-Functional, Establish Priorities, FDA (Food and Drug Administration), FDA Requirements, Leadership, Legal, Maintain Compliance, Marketing, Mentoring, Negotiation Skills, Outsourcing, Policy Implementation, Product Management, Product/Service Launch, Project/Program Management, Public Policy, Regulations, Regulatory Compliance, Service Delivery, Strategic Planning, Team Player, Willing to Travel
LOCATION
South San Francisco, CA
POSTED
1 day ago

Job Title: Senior Program Director, Commercial Regulatory Affairs
Location: South San Francisco CA
Type: Contract
Compensation: $120.00 - $122.40
Work Model: Remote
Hours: 40.0

Responsibilities

  • Lead Program Review Committees (PRCs) independently, managing complex product launches and cross-functional activities.
  • Act as the primary decision-maker for PRCs within your designated therapeutic or business area.
  • Develop and implement regulatory strategies, including preparing and submitting applications to health authorities.
  • Communicate effectively with the FDA and other regulatory bodies, sign-off on submissions, and address comments or requests.
  • Support development of cross-functional regulatory strategies, providing insights and recommendations.
  • Represent the company in official FDA communications and ensure compliance with evolving regulations.
  • Guide and mentor junior team members, fostering a collaborative and compliant work environment.
  • Participate in ad hoc projects and cross-functional teams to advance regulatory and organizational goals.

Requirements

  • Bachelor’s Degree in life sciences, law, public policy, marketing, business, education, or related discipline. Graduate-level Degree (JD, MBA, MS, PharmD, PhD) preferred.
  • 7+ years of experience in regulatory, legal, compliance, or related disciplines within the bio/pharma industry.
  • Regulatory advertising and promotion experience strongly preferred.
  • 4+ years of experience leading large-scale, cross-functional project teams or strategic initiatives.
  • In-depth knowledge of the bio/pharma industry, including compliance, legal, clinical, regulatory, and marketing aspects.
  • Strong influencing, negotiation, and communication skills, capable of guiding stakeholders at all levels.
  • Excellent project management skills with the ability to prioritize and coordinate multiple initiatives.
  • Ability to manage change effectively and foster innovation across teams.
  • Willingness to travel approximately 10% of the time.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

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Ref: #568-Clinical


About the Company

J

Joulé

With extensive scientific, clinical, and healthcare industry experience, Joulé recruiters excel at placing talent across core specialty areas:

  • Scientific staffing for hard-to-find skills

Working across every scientific discipline, Joulé places biologists, chemists, scientists, technicians and other specialists.

  • Clinical lifecycle recruiting

From research to regulations, safety to statistics, Joulé helps clients manage every stage of the clinical development lifecycle.

  • Equipment calibration, maintenance and validation

Laboratory and facility support comes with a total quality commitment backed by ISO 9001:2008 certification.

  • National healthcare recruitment

Trust Joulé’s extensive experience in physician, advanced practice provider and executive direct placement search.

COMPANY SIZE
500 to 999 employees
INDUSTRY
Biotechnology/Pharmaceuticals
WEBSITE
https://www.jouleinc.com/