Regulatory Marketing Communications and Advertising Reviewer (Medical Devices) J

Regulatory Marketing Communications and Advertising Reviewer (Medical Devices) Our leading healthcare / medical device client is seeking a Regulatory Marketing Communications and Advertising Intelligence Lead to add to their growing team! The Regulatory Marketing Communications and Advertising Reviewer is responsible for the review and approval of promotional materials. You will serve as the regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent with regulatory guidelines and enforcement trends governing the promotion of medical devices, policies, and business objectives. This is a 100% REMOTE opportunity with part-time hours (20-30 hours / week). Must work EST hours.ResponsibilitiesPerforms timely and accurate review of advertising and promotional material to meet internal timelines and requirements; provides regulatory guidance and expertise to the promotional review team.Evaluates advertising and promotional materials, communications, new campaigns, and launch strategies to ensure compliance with global regulations, guidance, brand standards, and policies and business objectives.Provides product development and label development strategies, as needed, to ensure promotional claims can be supported.Proposes creative, effective, and compliant regulatory strategies and solutions to challenging promotional concepts that meet business objectives and minimize regulatory risks.Researches and evaluates advertisement and promotional precedents for marketed products to assist with providing well-supported and clear guidance to key stakeholders.Maintains current awareness of evolving global and FDA regulations and interpretations, advisory letters, enforcement letters, and policy issues affecting the medical device industry. Communicates significant changes, potential risk, and impact to relevant stakeholders.Monitors competitor advertising to keep abreast of market promotional and advertising strategies.Fosters a business partnership environment with stakeholders to ensure the company meets strategic business objectives.Qualifications / Requirements : Detail-oriented with the ability to proofread and check documents for accuracy as well as consistency.Ability to deal with issues of critical importance; provides regulatory advice and recommendations involving regulatory issues on topics for which there may not be clear / specific regulatory guidance.Excellent oral and written skills, timeline responsibilities, negotiation skills. Works well with others, especially on a cross-functional team.BS degree in life / health science or related field and 6 years of experience in medical device regulatory affairs.Excellent project management, strong project leadership skills.Ability to meet multiple deadlines across a variety of projects / programs.The target hiring compensation range for this role is $60-80 / hr. Compensation is based on several factors including, but not limited to education, relevant work experience, relevant certifications, and location.#J-18808-Ljbffr

Salary : $60 - $80