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Director Regulatory Intelligence Jobs (NOW HIRING)

McKesson

Sr. Director, Regulatory Affairs

Richmond, VA · Hybrid

$148K - $195K/yr

The Sr. Director of Regulatory Affairs leads the development and execution of regulatory strategies ... Regulatory Intelligence & Sensing * Create programs to monitor the evolving regulatory landscape ...

McKesson

Sr. Director, Regulatory Affairs

Richmond, VA · Hybrid

$148K - $195K/yr

The Sr. Director of Regulatory Affairs leads the development and execution of regulatory strategies ... Regulatory Intelligence & Sensing * Create programs to monitor the evolving regulatory landscape ...

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Director Regulatory Intelligence information

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$91K

$176.2K

$248.5K

How much do director regulatory intelligence jobs pay per year?

As of Jul 7, 2026, the average yearly pay for director regulatory intelligence in the United States is $176,150.00, according to ZipRecruiter salary data. Most workers in this role earn between $150,000.00 and $198,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Director of Regulatory Intelligence, and why are they important?

To thrive as a Director of Regulatory Intelligence, you need deep expertise in regulatory affairs, strategic analysis, and industry guidelines, often backed by an advanced degree in life sciences or law. Familiarity with regulatory databases, global compliance platforms, and relevant certifications like RAC is highly beneficial. Exceptional communication, leadership, and critical thinking skills set successful candidates apart by enabling effective cross-functional collaboration and proactive risk management. These skills ensure that organizations stay ahead of regulatory changes, maintain compliance, and achieve business objectives in dynamic markets.

What is the difference between Director Regulatory Intelligence vs Regulatory Affairs Manager?

AspectDirector Regulatory IntelligenceRegulatory Affairs Manager
Required CredentialsBachelor's or Master’s in Life Sciences, Regulatory Affairs Certification (RAC)Bachelor's or Master’s in Life Sciences, Regulatory Affairs Certification (RAC)
Work EnvironmentStrategic, cross-functional teams, senior managementOperational, project management, compliance-focused
Employer & Industry UsagePharmaceutical, biotech, healthcare companiesPharmaceutical, biotech, healthcare companies
Search & Comparison IntentUnderstanding strategic regulatory rolesManaging regulatory submissions and compliance

The main difference is that the Director Regulatory Intelligence focuses on analyzing and interpreting regulatory trends to inform strategic decisions, while the Regulatory Affairs Manager handles day-to-day regulatory submissions and compliance activities. Both roles require similar credentials and are common in the pharmaceutical and biotech industries, but they differ in scope and strategic versus operational focus.

How does a Director of Regulatory Intelligence typically collaborate with cross-functional teams within an organization?

A Director of Regulatory Intelligence regularly partners with departments such as clinical, legal, quality, and R&D to interpret and communicate evolving regulatory requirements. This collaboration ensures that all functions are aligned with current global regulations and that strategic decisions are informed by the latest intelligence. Effective teamwork is critical for anticipating regulatory changes, guiding product development, and maintaining compliance across markets. Strong communication and relationship-building skills are essential, as the role often involves leading cross-functional meetings and providing actionable insights to senior leadership.

What does a Director of Regulatory Intelligence do?

A Director of Regulatory Intelligence is responsible for monitoring, analyzing, and interpreting regulatory trends, policies, and changes that could impact their organization, particularly in highly regulated industries like pharmaceuticals or medical devices. They lead teams to gather intelligence on global regulations, assess the potential impact on business strategies, and advise leadership on compliance and risk management. This role often involves liaising with regulatory agencies, developing strategies to address regulatory challenges, and ensuring the company's products and operations remain compliant with current and emerging regulations.
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Director Regulatory Intelligence jobs near you
Infographic showing various Director Regulatory Intelligence job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $176,150 per year, or $84.7 per hour.

Senior Director, Regulatory Affairs

Clinical Dynamix, Inc.

Jersey City, NJ

$164K - $216K/yr

Full-time

Posted 22 days ago

Be an early applicant

Job description

Senior Director, Regulatory Affairs - Northern NJ (Hybrid)

Client is seeking a capable, insightful, experienced Senior Director, Regulatory Affairs

Position Summary:

The Senior Director, Regulatory Affairs is responsible for providing subject matter expertise on matters related to global regulatory activities, as well as providing leadership for the growth and responsibilities of the regulatory department. The Senior Director will represent Company in key stakeholder and strategy meetings on regulatory matters related to medical product development and commercialization, including meetings with executive leadership, meetings with the Food and Drug Administration (FDA) and other regulators. This role leads preparation, review, and submission of documents to the FDA and other regulatory authorities to support product development leading to marketing authorization and lifecycle management. This role combines scientific, regulatory, and business knowledge to assure that Company products are developed and distributed according to all applicable regulations in alignment with the company’s strategic goals. The role requires a mastery of medical product regulations to develop efficient solutions to the evolving regulatory needs of the industry.

Responsibilities:

  • Secure US and global regulatory marketing authorization for new products, product updates, and product expansions. This includes preparation and filing of submissions, responding to regulatory authorities and auditors, and leading meetings with regulatory authorities.
  • Develop and implement a comprehensive set of policies, processes, and SOPs in support of the organization’s regulatory responsibility.
  • Formulate regulatory strategies for pipeline products.
  • Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develop strategies for resolution.
  • Perform global regulatory intelligence including monitoring regulatory updates, workshops, discussions, and other news sources.
  • Advance internal awareness of current and upcoming regulations, requirements, and expectations, and identify training and educational needs for the organization.
  • Manage processes involved with maintaining annual licenses, registrations, and listings.
  • Serve as an internal go-to subject matter expert on regulatory and quality matters.
  • Represent the company in external meetings on regulatory matters, including with regulators and auditors and development partners.

Requirements and Preferred Skills:

  • Advanced degree in Life Sciences required (PharmD, PhD, MD, MA)
  • 15+ years of progressive experience in regulatory affairs, with increasing scope of responsibility and demonstrated leadership at the global level
  • Knowledge of global regulatory agencies/processes/regulations
  • Record of successful medical product filings such as INDs, NDAs, BLAs, MAAs
  • Excellent writing and oral communication skills, with the ability to convey complex scientific and regulatory concepts clearly and persuasively
  • Ability to form and maintain working professional relationships with external stakeholders, regulatory authorities and scientific and clinical advisors
  • Prior experience and demonstrated ability to work in diverse therapeutic areas
  • Strong leadership skills with ability to set a vision, lead change, grow a team and mentor others
  • Experience leading regulatory authority communications and meetings