Associate Director Scientific Communications

vor 6 Monaten

Munich, Deutschland Regeneron Pharmaceuticals Inc. Vollzeit

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:

- Lexicon
- Scientific Platform
- Program Slides
- Disease-State Education materials
- Data/Publication updates
- 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

engagement activities

Fluency in English and German is required with the ability to read, write, comprehend,

and speak both
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.

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