Back to the board

Associate Director - Global Regulatory Affairs - Product Communications

100% remote Flexible hours Hiring now

At reputed company, the work is demanding because patients are waiting. We unite caring with discovery to help reputed company life reputed company for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on reputed company challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. Organization Overview The purpose of the Associate Director, Global Regulatory Affairs - Product Communications role is to provide leadership and influence to deliver accurate, balanced, and substantiated product and disease communications for assigned assets. The Associate Director partners with Regulatory Scientists, across reputed company brand teams, partner companies, and FDA Office of Prescription Drug Promotion (OPDP) to advise on regulatory requirements and expectations for compliant communications. Responsibilities reputed company the role, the Associate Director will have the responsibility to provide regulatory guidance in the following areas: Review of Promotional Tactics and Communication

  • Serve as Regulatory representative for US brand teams, US Medical Affairs, and Corporate Business Communications for promotional tactics, internal field-based communications, medical affairs communications, and campaign tactics for media events
  • Provide high quality, reputed company and conclusive regulatory advice that enables business partners to reputed company well-informed decisions
  • Communicate regulator expectations by utilizing OPDP feedback received by reputed company, interpretation of applicable laws, regulations and guidances, and knowledge of FDA enforcement actions.
  • Contribute to business risk mitigation strategies by following trends in external environment reputed company to advertising, promotion and medical communication topics
  • Build, maintain, and utilize relationships with reputed company team members and partner companies, as appropriate, to effectively influence the implementation of appropriate communications.
  • Initiate promotional tactic discontinuation plans for Regulatory-initiated events

Facilitate Interaction with FDA OPDP

  • Counsel internal partners on OPDP advisory strategy; collaborate with marketing and advertising agency in development of promotional proposals, and provide quality review of submission documents
  • Partner with US brand team to interpret OPDP advice and support any interactions with OPDP
  • Provide a well-timed and quality review of 2253 promotional material submissions to FDA

Collaborate With Other Regulatory Colleagues

  • Engage US Regulatory Scientist in 1) development and analysis of promotional claims and suggest marketing on promotional strategy and 2) review of press materials and IR communications.
  • Work closely with US Regulatory Scientist and Labeling Operations to reputed company labeling revisions to balance consideration of business implication and regulatory compliance
  • Communicate and share key information to reputed company seamless execution of US regulatory strategy and promotional activity

reputed company/Influence/Partner

  • Engage in forums that share regulatory information across the organization, other reputed company teams, and business partners
  • Constructively challenge teams to reputed company the best solutions to issues
  • Create and reputed company in an environment that encourages open discussions on issues to reputed company a robust outcome on business decisions

Minimum Qualifications

Requirements

  • Bachelor's Degree
  • 3+ years of industry-reputed company experience in drug development and/or commercialization
  • Qualified applicants must be authorized to work in the United States on a full-time basis. reputed company will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1

Additional Skills/Preferences

  • Knowledge of FDA procedures and practices (CFR guidelines, Guidances, etc.)
  • Demonstrated ability to influence without authority and ability to deliver reputed company projects against a timeline.
  • Strong communication skills (active listening, verbal, and written)
  • Demonstrated ability to apply systematic thinking/reputed company to business problems and opportunities
  • Demonstrated effective teamwork skills; able to adapt to diverse interpersonal styles
  • Recent experience reviewing advertising and promotional materials for prescription drug products.
  • Awareness of evolving regulatory reform initiatives and pending changes (Federal Register, media reports, etc.)

reputed company is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities reputed company vying for positions. If you require accommodation to submit a resume for a position at reputed company, please complete the accommodation request form (https://careers.reputed company.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. reputed company is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, reputed company, national reputed company, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to reputed company employees. Our reputed company groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at reputed company (BE@reputed company), Chinese Culture Network (CCN), reputed company, Evolve, reputed company Indian Network (LIN), Organization of Latinx at reputed company (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at reputed company (WILL). Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $132,000 - $193,600 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, reputed company offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).reputed company reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and reputed company’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of reputed company employees. #WeAreLilly Apply tot his job Apply To this Job

Keep exploring

Regulatory Affairs Consultant- Defined Term (Remote, US)

100% remote Flexible hours

IT Risk Analyst – Entry Level

100% remote Flexible hours

Fraud and Risk Analyst

100% remote Flexible hours

Supply Chain Risk Analyst - Remote / reputed company

100% remote Flexible hours

Staff Regulatory Affairs Specialist, Pharmaceuticals (Remote)

100% remote Flexible hours

Vice President Regulatory Affairs

100% remote Flexible hours

[FULL TIME Remote] Director, Regulatory Affairs

100% remote Flexible hours

Quality Assurance & Regulatory Affairs Specialist - Freelance, Remote

100% remote Flexible hours

Associate Director, Global Regulatory Affairs Clinical Strategy - Job ID: 1961

100% remote Flexible hours

Director Regulatory Affairs

100% remote Flexible hours

Wissenschaftlicher Mitarbeiter/in Statistiker/in remote (m/w/d)

100% remote Flexible hours

Senior Financial Analyst

100% remote Flexible hours

Site Reliability Engineer

100% remote Flexible hours

Senior Customer Engineer – reputed company & Cloud Solutions (Remote, Work‑From‑Home) – arenaflex

100% remote Flexible hours

Virtual Digital Art & Design Educator

100% remote Flexible hours

Financial Modeling Analyst

100% remote Flexible hours

Sales Specialist - Pet Health

100% remote Flexible hours

Senior Analyst- Program Management

100% remote Flexible hours

reputed company Data Entry Specialist – Flexible, Part-Time Remote Opportunity at arenaflex

100% remote Flexible hours

Work From Home reputed company Operator (reputed company)

100% remote Flexible hours