Job Description
Perrigo Company is dedicated to making lives better by bringing Quality, Affordable Self-care products that consumers trust everywhere they are sold.
Help us do it.Description Overview
This role focuses on substantiation and management of safety and health benefit claims for new and established brands and products within the CSCI OTC organisation.
The Scientific Affairs Manager leads on proving efficacy to drive competitive claims throughout product lifecycle and partners with Product Developers to develop superior products.
He/she communicates internally and externally to our Regulators, Health Care Professionals, Key Opinion Leaders, Customers and Consumers to drive acceptance, awareness, and recommendation.
The role is highly driven by consumer-centricity.Scope of the Role
- Lead identification and substantiation of health benefit claims, with an understanding of appropriate terminology and language;
- Work closely with Product Development, Marketing and Regulatory colleagues to ensure a consolidated understanding of product MoA and ensure all claim options are explored;
- Lead design of preclinical and/or clinical studies needed to support health benefit claims;
- Collaborate closely with Clinical Operations during study management;
- Provide projectlevel expertise, working with Marketing, Formulation, Product Development, Packaging, Project Management, Regulatory and Consumer Insight functions internally, and with external partners, according to applicable regulations and guidance, ICH-GCP and Perrigo SOPs;
- Author, update and maintain relevant scientific documentation;
- Communicate internally and externally to drive acceptance, awareness and recommendation of consumer selfcare products;
- Contribute to the development of inhouse Scientific Affairs expertise to ensure high quality, credible and relevant data is generated to support new/existing products, support publication of this data, and KOL management when appropriate;
- Landscape surveying for new trends & emerging technologies.
- Typically 5+ years' experience in scientific affairs and clinical development.
- Experience in preclinical and clinical development of medical devices and medicines, especially smoking cessation, is highly desired, alongside a proven track record in study design methodology and claims management.
- Applicants should have strong communication and stakeholder management skills.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.
Our full Equal Employment Opportunity and Affirmative Action Policy Statement is available on our main career site in English and Spanish and will be provided in other accessible forms for persons with disabilities.
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