EPM Scientific - Phaidon International
Associate Director of Regulatory Affairs - Ad/Promo
EPM Scientific - Phaidon International, Lakewood, New Jersey, us, 08701
Summary:
Maximise your chances of a successful application to this job by ensuring your CV and skills are a good match.A global health care company, dedicated to improving people's lives through innovative solutions specialised in pharmaceuticals, medical devices, and over-the-counter products is looking to bring on an Associate Director of Regulatory Affairs Ad/Promo to join their team! The Ad/Promo team is rapidly growing, and they are looking for someone to come in and provide their expertise, based out of their New Jersey office. This role will give you an amazing opportunity to contribute to the companies mission to enrich lives by delivering better health outcomes.The Associate Director will be responsible for…Reviewing Ad/Promo materials, new campaigns, and launch strategies for assigned products to ensure regulatory compliance. Ensure timely and accurate evaluation to meet deadlines and requirementsDeveloping and implement regulatory strategies and solutions to ensure all ad/promo material comply with regulatory requirements and company policiesMonitoring FDA activities, including enforcement actions and guidance documents, to assess their impact on company productsEnsuring that promotional package inserts and important safety information are updated as necessaryThe Associate Director should have the following qualifications:Bachelor's degree is required in Life Science or related field; Advanced degree (MS, MD, PhD, PharmD) preferredMinimum of 8 years of pharmaceutical experience; 4+ years of prescription product ad/promo review experienceWorking knowledge of the Rx product NDA and labeling processesCourse training in ad/promo reviewStrong interpersonal skills, ability to work on a team, and communication skillsBenefits:Medical, Dental and Vision insurance401(k) matchingTuition reimbursementCommuter benefits
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Maximise your chances of a successful application to this job by ensuring your CV and skills are a good match.A global health care company, dedicated to improving people's lives through innovative solutions specialised in pharmaceuticals, medical devices, and over-the-counter products is looking to bring on an Associate Director of Regulatory Affairs Ad/Promo to join their team! The Ad/Promo team is rapidly growing, and they are looking for someone to come in and provide their expertise, based out of their New Jersey office. This role will give you an amazing opportunity to contribute to the companies mission to enrich lives by delivering better health outcomes.The Associate Director will be responsible for…Reviewing Ad/Promo materials, new campaigns, and launch strategies for assigned products to ensure regulatory compliance. Ensure timely and accurate evaluation to meet deadlines and requirementsDeveloping and implement regulatory strategies and solutions to ensure all ad/promo material comply with regulatory requirements and company policiesMonitoring FDA activities, including enforcement actions and guidance documents, to assess their impact on company productsEnsuring that promotional package inserts and important safety information are updated as necessaryThe Associate Director should have the following qualifications:Bachelor's degree is required in Life Science or related field; Advanced degree (MS, MD, PhD, PharmD) preferredMinimum of 8 years of pharmaceutical experience; 4+ years of prescription product ad/promo review experienceWorking knowledge of the Rx product NDA and labeling processesCourse training in ad/promo reviewStrong interpersonal skills, ability to work on a team, and communication skillsBenefits:Medical, Dental and Vision insurance401(k) matchingTuition reimbursementCommuter benefits
#J-18808-Ljbffr