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Associate Director Scientific Communications

3 months ago

Baltimore, United States Regeneron Pharmaceuticals Full time

Associate Director Scientific Communications - Germany

As an Associate Director Scientific Communications, you will drive the development, alignment, and country level adaptation of the global scientific communications plan for the Oncology Medical Affairs portfolio. You will work in strategic partnership with the country level Medical Affairs Franchise Directors and the Global Lead of Scientific Communications to develop communications goals specific to the German Healthcare Community. The primary responsibilities are to adapt the global scientific communications platforms and lexicons, and other assets, to ensure the delivery of country relevant content in line with the vision of the comprehensive global scientific communication plans.

A typical day may include the following: Strategizing and benchmarking scientific communication needs and opportunities in Germany whilst liaising with key stakeholders within the region, prioritizing regional scientific educational opportunities. Working closely with the Global and/or EU Scientific Communications partners and Global, EU, or/and local Franchise Medical Affairs Director(s) to drive the quality control and endorsement of: - Scientific Platform - Program Slides - Disease-State Education materials - Field Medical Training materials - Congress materials Adhering to clear regionally meaningful Scientific Communications goals and ensuring compliant execution according to German regulations Participating in cross-functional discussions to align on congress deliverables Assisting adherence to country/region level regulatory guidance Collaborating to: - adapt medical content for regional congresses, and leads some of these activities, particularly adapting to regional needs; - assess regional internal and external medical education needs and develop educational activities Leading projects through the appropriate medical review committees for approval of materials in Germany Ensuring medical and scientific integrity and accuracy of all assets, verifying that materials have a fair and balanced representation Developing centralized, organized, and searchable resource repositories for the German internal teams Working with Project Managers to supervise all materials are delivered within the allocated budget, and tracks budget spend in a systematic manner Adhering to the highest ethical and compliance standards and a high bar personal ethics This may be for you if: You have a “patient first” value system You are inquisitive, have a can-do spirit, and a hands-on execution mentality You are able to work effectively in a fast paced, constantly evolving and expanding organization To be considered for this position, you are required to have a PhD, MD, or PharmD along with 6+ years experience in the pharmaceutical industry, including >4 years in Scientific Communications and/or Medical Affairs, with a strong background in oncology. Familiarity with the EFPIA Code, as well as with the FSA, AKG and Progenerika industry codes, is required. Additional qualifications include: Familiarity with communication strategies and understanding of scientific communications platform goals and structure Ability to provide insights into scientific communication planning and expert Fluency in English and German is required with the ability to read, write, comprehend and speak both Does this sound like you? Apply now to take your first step towards living the Regeneron Way We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location. Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

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