New · posted Oct 15
Mirum Pharmaceuticals · Pharmaceuticals
Associate Director, Regulatory Affairs Advertising and Promotion
- Foster City, CA
- Hybrid
- Full-time
- Director
Open until filled
The role
The Associate Director, Regulatory Affairs Advertising and Promotion provides regulatory guidance on commercial regulatory activities to enable the business to meet its commercial needs in a compliant manner. This position will provide regulatory guidance as a member of the Medical, Legal and Regulatory (MLR). This role is accountable for helping develop strategies and timelines, and managing internal team discussions to support preparation of advertising and promotional materials for regulatory submissions. This role will report to the Director, Global Regulatory Affairs Advertising and Promotion.
MISSION
Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.
What you need
Education /Experience
- Bachelor’s or advanced degree in a scientific discipline, with a minimum of 8 years in Regulatory Affairs with a minimum of 6 years of experience in the regulatory review of advertising and promotional materials for prescription drug and/or biologic products.
- Experience representing Commercial Regulatory Affairs on cross functional teams is desirable.
- Excellent planning and organizational skills and the ability to work simultaneously on multiple projects with tight timelines.
- Excellent communication skills both in writing and verbally.
Knowledge, Skills and Abilities
- Experience with FDA’s Office of Prescription Drug Promotion (OPDP) submissions and strategies.
- In-depth knowledge of regulatory requirements associated with advertising and promotion of prescription drug products is required.
- Knowledge of and experience with laws and regulations regarding marketing pharmaceuticals in rest of world (ROW) is highly desired.
- Excellent verbal, written, negotiation, influence and interpersonal communication skills are required.
- Capable of critically reviewing complex technical/scientific documents and influencing colleagues across functions.
- Requires ability to work both independently and in a team environment, to set priorities to meet timelines, to influence others.
- Ability to engage multiple stakeholders to achieve the business objective.
- Organized with systematic approach to prioritization.
- Process oriented to achieve the business objective.
Skills named in this posting
Pay
$205,000 – $225,000 a year
Employer providedThe salary range for this position is $205,000 to $225,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.
Where you'll work
Foster City, CAHybridOpen in Maps (opens in a new tab)
More jobs in Foster City, CAWorking conditions
- This is a high growth, fast paced organization. The ability to be productive and successful in a work environment is critical.
- Some travel required. Responsibilities may require a work schedule that may include working outside of “normal” work hours, to meet business demands of a global company.
JOB FUNCTIONS/RESPONSIBILITIES
- Responsible for providing commercial regulatory oversight for assigned programs.
- Manage and author commercial regulatory submissions, working closely with the Publishing vendor to ensure timely publishing and submission of promotional materials to the Office of Prescription Drug Promotion (OPDP).
- Provide regulatory guidance on new concepts and new campaigns.
- Maintain a continued awareness and understanding of FDA regulations, guidance documents, and enforcement actions with regards to advertising and promotion of pharmaceutical products. Help monitor enforcement trends and provide timely advice to the team.
- Recognized as a resource for commercial regulatory advice across departments.
- May contribute to process improvements relevant to commercial regulatory activities, including the MLR Committee.
- Aid in the development and implementation of regulatory advertising and promotional processes, as necessary.
Equal opportunity, accessibility and legal noticesMirum Pharmaceuticals's statements, word for word
Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.
Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is 5% above the US median for Labeling & Promotion roles at this level.
This roleEmployer provided
Director roles in California11 roles publishing pay
Director roles in the US35 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $205,000 | — | $225,000 |
| California (middle half) | $205,500 | $210,000 | $237,000 |
| All US (middle half) | $197,500 | $205,500 | $216,750 |
This role: Mirum Pharmaceuticals's own published range. Comparisons: the base pay employers published on open Labeling & Promotion roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Labeling & Promotion
The general path across 74 open Labeling & Promotion roles on Regulatory Jobs, with the titles they carry most. Not Mirum Pharmaceuticals's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 15 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership7
- Documentation and SOPs3
- Regulatory submissions2
- GMP and compliance1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
From Regulatory News
Manufacturing and quality coverage for this professionCompany hiring pulse
Mirum Pharmaceuticals on Regulatory Jobs
- 7
- Open roles
- 7
- Distinct roles
- 1
- Locations
By discipline
- Regulatory5 71%
- Quality2 29%
By level
- Director5 71%
- VP & Executive1 14%
- Manager1 14%
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Associate Director, Regulatory Affairs Advertising and Promotion at Mirum Pharmaceuticals
Open until filled. $205K–$225K a year, employer provided.