Director, Regulatory Affairs Advertising & Promotion
$193.4k - $241.8kAcadia Pharmaceuticals
Regulatory Affairs Manager
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.
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.
Acadia Pharmaceuticals$193.4k - $241.8k
Position Summary Responsible for leading regulatory review of advertising, promotional, and other external communications to ensure compliance with applicable... .... ~10 years progressively responsible Regulatory Affairs experience focused on advertising/promotional regulations...SuggestedWork at office3 days per week- ...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
- Scorpion Therapeutics is seeking a Regulatory Affairs Leader in San Diego, CA to oversee compliance on advertising and promotional materials. The successful candidate will lead regulatory review processes and provide strategic guidance, ensuring timely approval of materials...Suggested
- ...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...Suggested
$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
- ...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...Contract work
$189k - $246k
...forge new paths as we move toward a common goal of elevating science and service for rare patients.Position Summary:The Director, Regulatory Affairs Strategy is responsible for developing and executing global regulatory strategies for Phase 2 and Phase 3 development programs...Temporary workLocal area- Stryker Corporation is looking for a Director of Regulatory Affairs to lead regulatory strategy and compliance efforts. This fully remote position involves coordination with FDA and overseeing regulatory submissions in the pharma/biotech field. Candidates should have extensive...Remote job
$220k - $245k
...Fate Therapeutic is seeking a strategic and experienced Director, Regulatory Affairs to lead global clinical regulatory activities supporting innovative biotechnology development programs. This role will oversee INDs, CTAs, amendments, DSURs, and Health Authority interactions...Full time$90k - $105k
...America on safety matters while promoting best practices that improve jobsite safety, regulatory compliance, and workforce... ...Communications With the assistance of the Director of Workforce Development,... ...with AGC of America’s government affairs liaison for regulation updates....Contract workFor contractorsApprenticeshipWork experience placementLocal areaMonday to FridayFlexible hoursDay shift$130.8k - $179k
...escalating issues to Clinical Compliance (CC) Director when necessary. Serves as the ClinOps... ...leads when necessary. Participates and promotes collaboration in departmental and cross‑... .... Demonstrates knowledge of applicable regulatory requirements, and business standards....- ...Senior Executive Director, Regulatory Affairs About the Company Well-funded clinical-stage biotech company Industry Biotechnology Type Privately Held About the Role The Company is seeking a Senior Executive Director for Regulatory Affairs...
$252.5k - $344k
...Executive Director, Regulatory Strategy Endocrinology Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company... ...relationships Cultivates a workforce through hiring, promotion, and staff development aligned with current and emerging talent...$87k - $195k
...audit plans, monitoring activities, and gap analyses. Translate regulatory and payer requirements into practical controls, training, and... ...work schedules and a discretionary time off policy to promote work‑life balance and help employees lead fulfilling lives. Learn...Local areaFlexible hours$240k - $275k
...Senior Director, Global Regulatory Affairs The Senior Director, Global Regulatory Affairs will provide strategic regulatory leadership across Janux's clinical-stage oncology pipeline, supporting programs from early development through registration. This individual will...Full timeSummer workWork at officeRemote workRelocation packageMonday to FridayShift work- ...Executive Director, CMC Regulatory Affairs About the Company An oncology biotech developing mid-stage clinical programs and CMC regulatory strategies. Industry Biotechnology Type Privately Held About the Role The Company is seeking a Senior Director...
- ...Executive Director, Regulatory Affairs About the Company Esteemed company developing medicines for inflammatory & autoimmune diseases Industry Biotechnology Type Privately Held, VC-backed Founded 2018 Employees 51-200 Funding $101-$200 million...
$158.1k - $216k
...Regulatory Affairs Manager Responsible for leading the regulatory review of medical education and commercial advertising and promotional materials for product, disease state, and training/education programs. Leads the Promotional Review Committee (PRC) process for assigned...Work at office- ...Regulatory Manager - IVD And 510(K) We are seeking a highly motivated and experienced... ...Regulatory Specialist to join our Regulatory Affairs team. The ideal candidate will have a... ...and provide input on product labeling, promotional materials, and change controls to...
$210k - $230k
...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...$107.16k - $226.32k
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...Local area$180k - $230k
...The Position The Associate Director/Director of Drug Safety & Pharmacovigilance (PV) Quality... ..., and alliance management activities, promoting inspection readiness and maintaining a... ...processes and systems to ensure compliance with regulatory requirements and internal policies....$207.5k - $281k
...Principal Regulatory Compliance Manager Come join our team of leaders, learners, and world-class compliance professionals. We are part... ..., compliance committees, and executive stakeholders. Promote a culture of compliance as a strategic advantage, operating as...3 days per week$141.6k - $212.4k
...sequencing, family planning, health/dental/vision, retirement benefits, and paid time off.### We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation,...Local area$150k - $194k
...Associate Director, Regulatory Affairs CMC page is loaded## Associate Director, Regulatory Affairs CMCremote type: Remotelocations: Remotetime type: Full timeposted on: Posted Yesterdayjob requisition id: JR000594Crinetics is a pharmaceutical company based in San Diego...Contract workLocal area- ...procedures as well as advising the client on various economic and regulatory risks in a specific industry field of expertise by identifying... ...development and marketing Has knowledge of and can promote the use of all BDO client service specialties/offerings, including...Work at office
$132.7k - $182k
...Regulatory Affairs Specialist Responsible for supporting regulatory strategy execution for development programs. Works closely with the Director of Regulatory Affairs to prepare regulatory submissions (strategy, authoring, timeline planning, etc.) and to maintain department...Local area- ...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...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Director, Regulatory Affairs Advertising & Promotion. Be the first to apply!
- regulatory affairs director San Diego, CA
- senior regulatory manager San Diego, CA
- senior director regulatory affairs San Diego, CA
- regulatory affairs manager medical devices San Diego, CA
- compliance director San Diego, CA
- regulatory affairs manager pharmaceutical San Diego, CA
- regulatory manager San Diego, CA
- regulatory & compliance manager San Diego, CA
- director global regulatory affairs San Diego, CA
- head compliance San Diego, CA


