[Hiring] Associate Director - Global Regulatory Affairs - Product Communications @reputed company

Role Description 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

• 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

Qualifications

• 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.)

Benefits

• 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)
• 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

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