Associate Director, Regulatory Affairs Advertising & Promotion
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Job Location:
Florham Park, NJ - USA
Monthly Salary:
Not Disclosed
Posted on:
2 hours ago
Vacancies:
1 Vacancy
Job Summary
The Associate Director Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional multidisciplinary therapeutic teams and executes multidivisional initiatives. The Associate Director envisions the future by using global marketplace technology and business knowledge collects and analyzes issues and trends that affect the business identifies and acts upon cross-organization or cross-business opportunities and possesses and leverages broad industry knowledge.
Responsibilities:
- Make decisions and plans for operations (workflow assignments staff development) within area of responsibility with minimal direction. Sets strategy and leads cross-functional/multidisciplinary therapeutic teams and multidivisional initiatives.
- Maintains and evaluates productivity metrics to project current and future business needs
- Aligns and maintains effective communication channels with key Medical Marketing Regulatory Legal and Public Affairs counterparts. Identifies areas of improvement in process/policy develops recommendations/plan and leads initiatives.
- Assists in the management of the departmental budget identifies and communicates budgetary needs to Operations and Finance and identifies and projects current and future expenditures and business needs.
- Operates independently with recognition of when to consult departmental senior concerning absence of Director is responsible for day-to-day operations. Responsible for departmental initiatives which have significant impact on both internal and external customers.
- Encourages innovation and holds employees accountable for delivering on their goals; recognizes mentors rewards and recommends promotion for staff members based on their performance results and development.
- Exhibits solid understanding of regulations and guidance of regulatory authorities political and legal climate and industry practices related to advertising and promotions to assist in meeting organizational goals. Possesses and leverages broad industry knowledge
- Develops and implements complex processes and projects and develops and delivers strategic presentations for senior management
- Identifies areas of improvement in process policy develops recommendations/plan and leads initiatives
- This role will work a hybrid work schedule (3 days in office) from our AbbVie Mettawa IL or Florham Park NJ headquarters.
Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required
Qualifications :
- Bachelors degree plus 8 years of relevant experience (e.g. Applicable pharmaceutical/medical devices/biologics experience pharmacy rotations Public Health etc.)
- Advanced degree preferred: MS MPH MSN PA DNP PhD PharmD JD MD degree plus 6 years of relevant industry experience. Certification a plus.
- Experience in US Regulatory Affairs Advertising and Promotion highly preferred
- Experience working in a complex and matrix environment
- Strong communication skills both oral and written
- Experience developing and implementing successful global regulatory strategies
- Experience in management capacity preferred
Additional Information :
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this postingbased on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately paymore or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commissionincentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and untilpaid and may be modified at the Companys sole and absolute discretion consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Full-time
Key Skills
- Proofreading
- Adobe Acrobat
- FDA Regulations
- Manufacturing & Controls
- Biotechnology
- Clinical Trials
- Research & Development
- GLP
- cGMP
- Product Development
- Chemistry
- Writing Skills
About Company
AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more
