Director, Regulatory Affairs Advertising & Promotion
$193.4k - $241.8kAcadia Pharmaceuticals Inc.
About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer’s disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we’re here to be their difference. Please note that this position can be based in San Diego, CA; Princeton, NJ; San Francisco, CA. Acadia's hybrid model requires this role to work in our office an average of 3 days per week. Position Summary Responsible for leading the regulatory review of advertising, promotional, and other external communications to ensure compliance with applicable regulatory requirements while supporting Acadia's commercial objectives. This role oversees the development, review, and maintenance of product labeling and provides regulatory guidance throughout the Medical, Legal, and Regulatory (MLR) review process. The position partners closely with cross-functional teams to support the timely approval and distribution of promotional and disease state materials, serves as the primary liaison with the FDA's Office of Prescription Drug Promotion (OPDP) for advertising and promotional submissions, and contributes to labeling strategies for regulatory submissions across Acadia's product portfolio. Primary Responsibilities Leads the development and oversight of the processes and procedures relevant to the creation, review and approval of advertising and promotional materials as part of Acadia Medical, Legal and Regulatory review process and other external communication to ensure regulatory compliance. Reviews external communications materials, sales and marketing materials, including training, for compliance to current regulations and guidance. Represents the regulatory department with senior management on regulatory strategy and risk analysis as it relates to Acadia’s commercial strategy and compliance. Participates in training for sales and marketing on advertising and promotional material. Represents the company to outside customers and agencies and makes presentations as needed on current regulatory issues pertaining to advertising and promotional activities. Other responsibilities as assigned Education/Experience/Skills Bachelor’s degree in a scientific discipline or related field. MBA preferred. Targeting 10 years progressively responsible Regulatory Affairs experience with a focus on advertising and promotional regulations. An equivalent combination of relevant education and experience may be considered. Experience communicating and negotiating directly with OPDP and performing risk assessment. Significant demonstrated experience developing and executing complex and innovative global regulatory strategies, assessing & communicating risk/benefit to senior management, and influencing organizational direction as it pertains to compliance advertising and promotion materials. Experience with labeling development and life-cycle management Experience involving complex negotiations with regulatory authorities. Experience in organizational management, including matrix management of senior professionals and higher-level project teams. Thorough knowledge of US and international regulations, as they apply to pharmaceutical drug development. Demonstrated problem solving abilities and conflict resolution skills. Excellent verbal and written organizational and communication skills; Experience influencing and communicating policy issues. Excellent collaboration skills with demonstrated ability to work effectively in cross-functional and/or global teams. Skilled at negotiating with business partners or management and influencing senior level leaders regarding matters of significance to the organization. Proficient at creating and communicating a clear vision among team members effectively aligning resources and activities to achieve functional area and/or organizational goals Must be willing and able to travel both domestically and internationally. Physical Requirements This role involves regular standing, walking, sitting, and the use of hands for handling or operating equipment. The employee may also need to reach, climb, balance, stoop, kneel, crouch, and maintain visual, verbal, and auditory communication in a standard office environment and while working independently from remote locations. The employee must occasionally lift and/or move up to 20 pounds. This position requires the ability to travel independently overnight and/or work after hours as required by travel schedules or business needs.
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In addition to a competitive base salary, this position is also eligible for discretionary bonus and equity awards based on factors such as individual and organizational performance. Actual amounts will vary depending on experience, performance, and location. Salary Range$193,400—$241,800 USD
What we offer US-based Employees: Competitive base, bonus, new hire and ongoing equity packages Medical, dental, and vision insurance Employer-paid life, disability, business travel and EAP coverage 401(k) Plan with a fully vested company match 1:1 up to 5% Employee Stock Purchase Plan with a 2-year purchase price lock-in 15+ vacation days 13 -15 paid holidays, including office closure between December 24th and January 1st 10 days of paid sick time Paid parental leave benefit Tuition assistance EEO Statement (US-based Employees): Studies have shown that women and people of color are less likely to apply for jobs unless they believe they meet every one of the qualifications in the exact way they are described in job postings. We are committed to building a diverse, equitable, inclusive, and innovative company, and we are looking for the BEST candidate for the job. That candidate may be one who comes from a less traditional background or may meet the qualifications in a different way. We strongly encourage you to apply, especially if the reason you are the best candidate isn’t exactly what we describe here. It is the policy of Acadia to provide equal employment opportunities to all employees and employment applicants without regard to considerations of race, including related to hairstyle, color, religion or religious creed, sexual orientation, gender, gender identity, gender expression, gender transition, country of origin, ancestry, citizenship, age, physical or mental disability, genetic information, legally-protected medical condition or information, marital status, domestic partner status, family care status, military caregiver status, veteran or military status (including reserve status, National Guard status, and military service or obligation), status as a victim of domestic violence, sexual assault or stalking, enrollment in a public assistance program, or any basis protected under federal, state or local law. As an equal opportunity employer, Acadia is committed to a diverse workforce. If you are a qualified individual with a disability or a disabled veteran, you have the right to request a reasonable accommodation. Furthermore, you may request additional support if you are unable or limited in your ability to use or access Acadia’s career website due to your disability, along with any accommodations throughout the interview process. To request or inquire about your reasonable accommodation, please complete our Reasonable Accommodation Request Form or contact us at View email address on click.appcast.io or View phone number on click.appcast.io. Please note that reasonable accommodations granted throughout the recruiting process are not guaranteed to be the same accommodations given if hired. A new request will need to be submitted for any ADA accommodations after starting employment. California Applicants: Please see Additional Information for California Residents within our Privacy Policy. Canadian Applicants: Please see Additional Information for Canadian Residents within our Privacy Policy. Applicants in the European Economic Area, Switzerland, the United Kingdom, and Serbia: Please see Additional Information for Individuals in the European Economic Area, Switzerland, the United Kingdom, and Serbia within our Privacy Policy. Notice to Search Firms/Third-Party Recruitment Agencies (Recruiters): The Talent Acquisition team manages the recruitment and employment process for Acadia Pharmaceuticals Inc. (“Acadia”). Acadia does not accept resumes from recruiters or search firms without an executed search agreement in place. Resumes sent to Acadia employees in the absence of an executed search agreement will not obligate Acadia in any way with respect to the future employment of those individuals or potential remuneration to any recruiter or search firm. Candidates should never be submitted directly to our hiring managers or employees.- ...Head of Global Regulatory Advertising and Promotion About the Company Industry shaping biopharmaceutical company Industry Biotechnology Type Public Company About the Role The Company is seeking a Head of Global Regulatory Advertising and Promotion...Suggested
- ...The Director of Regulatory Affairs will be based in San Diego, CA. The role includes but is not limited to the development and implementation... ...documentation for compliance programs such as labeling, promotional material review, and other regulatory requirements. This...SuggestedWork experience placementWork at office
$220k - $245k
...Responsibilities Lead regulatory activities for filing INDs, CTAs, and maintenance activities for open applications, including DSURs... ...life science with at least 10 years of experience in Regulatory Affairs in the biotechnology or pharmaceutical industry; PhD degree...Suggested- ...Regulatory Cmc Leadership Role Responsible for the strategic regulatory CMC leadership for assigned commercial products to ensure regulatory... ...: BS/BA degree AND 12+ years experience in Regulatory Affairs in the Pharmaceutical/Biotech industry. Prior project...SuggestedContract work
$130k - $250k
...Director, Regulatory Affairs FULLY REMOTE Assignment through Temporary Agency - Approximately 6 Months Approximately 40 Hours Per Week... ...based on any protected status. Mapp uses a wide variety of advertising and outreach to find qualified applicants for employment....SuggestedFull timeTemporary workFor contractorsRemote work- ...Fate Therapeutics, Inc. is seeking a Director, Regulatory Affairs to manage global clinical regulatory activities in innovative biotechnology programs. This role includes overseeing IND submissions, ensuring FDA compliance, and collaborating with cross-functional teams...Full time
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...therapies to patients in need. The Position The Director of Regulatory Affairs is Arrowhead's Labeling lead, who drives cross-functional... ...two or more major geographic areas. Knowledge of advertising promotion regulations and FDA Guidance documents issued with...$150k - $194k
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At KPMG, you can become an integral part of a dynamic team at one of the worlds top tax firms. Enjoy a collaborative, future-forward culture that empowers your success. Work with KPMGs extensive network of specialists; enjoy access to our Ignition Centers, where deep industry...Full timeLocal area$141.6k - $212.4k
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...The Position The Associate Director/ Director of Drug Safety & Pharmacovigilance... ...alliance management activities, thus always promoting inspection readiness and maintaining a robust... ...to ensure compliance/alignment with regulatory requirements and internal policies/...- ...from other Teledyne office locations. ** Job Summary The Director, Customs Compliance – Americas is responsible for the... ...audit management, as well as the ability to translate complex regulatory requirements into practical, business‑aligned solutions. The Director...Work experience placementWork at officeLocal areaRemote work
- ...Chief Commercial Officer (CCO) About the Company We are an international full-service media buying and advertising company developing its own ad products. Industry Marketing and Advertising Type Privately Held About the Role The Company is seeking...
- ...What The Role Is The Manager, Regulatory Compliance, will assist in the management of the Clearway Energy Group electric regulatory compliance program and in administering, facilitating, and managing compliance with NERC and other federal electric regulatory requirements...H1bWork at officeVisa sponsorship
- ...executing compliance obligations and embedding AML requirements in product design. Candidates should have over 5 years experience in regulatory compliance and strong communication skills. This is a hybrid position in San Diego, offering competitive pay and diverse...
$228k - $245k
...A biotechnology firm is seeking a Director of Global Regulatory Affairs in San Diego. This role involves developing and executing regulatory strategies to support clinical programs and interaction with global regulatory agencies. Candidates should have a BS in life sciences...- Travere Therapeutics is looking for a Director of Regulatory Affairs Strategy based in San Diego, California. This role will develop and execute global regulatory strategies for Phase 2 and Phase 3 development programs, ensuring alignment with regulatory requirements while...
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$214k - $268k
Senior Director, Pharmaceutical Strategy and Development Leader page is loaded## Senior Director... ...collaborate with Clinical, Commercial, Regulatory, and other functional areas to integrate... ...submissions and briefing booklets.* Promote best practices and lead improvement...Local area$112k - $153k
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- This Director position is located at our new HQ in La Jolla. Eligible to participate in... ...and ensures adherence to all applicable regulatory requirements. Key Responsibilities Gift... ...Program Marketing and Outreach Strategically promote the Gift Planning Program through...
$175k - $200k
...workload ~ Review team members' work schedules/tasks ~ Monitor and evaluate engineers' progress ~ Support and promote a culture that rewards motivation and cooperation ~ Coordinate work with other managers and staff ~ Participate...Long term contractPermanent employmentFull timeContract workFor contractorsFor subcontractorFlexible hours$112k - $153k
...levels, contributing to the Inspection Readiness framework and promoting a continuous quality mindset across Sobi. Author GCP QA... ...GCP guidelines, industry best practices, and FDA, EMA and other regulatory requirements. Understanding of quality assurance activities principles...Temporary workLocal areaFlexible hours$156.5k - $211.5k
Intuit Inc. is seeking a Compliance Manager in San Diego focusing on consumer protection regulations such as EFTA and FCRA. This role emphasizes compliance oversight for financial products and involves working closely with various stakeholders to develop clear product requirements...$220.6k - $275.7k
...days per week on average. Position Summary The Senior Director, Regulatory Operations provides strategic and operational leadership for... .... This role is a key member of the Global Regulatory Affairs Leadership Team and plays a critical role in driving operational...Work at officeLocal areaRemote workWorldwideNight shift3 days per week$220.6k - $275.7k
...Primary Responsibilities Lead and scale global Regulatory Operations (organizational design, talent strategy, performance management).... ...scalable solutions. Champion digital transformation in Regulatory Affairs, including AI/advanced analytics to improve submission...Worldwide
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