Associate Director, Medical Information
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Job Location:
Warren, OH - USA
Monthly Salary:
$ 157200 - 256600
Posted on:
7 days ago
Vacancies:
1 Vacancy
Job Summary
As Associate Director Medical Information you will lead scientific communication and medical information strategy for assigned therapeutic areas enabling high-quality compliant scientific exchange with healthcare professionals patients and internal team members. You will manage the tactical execution of Global and US Medical Affairs medical information plans convert insights into strategic recommendations and serve as a trusted partner. We ensure excellence in delivery while maintaining full adherence to company policies procedures and all regulations and industry standards.
Where & When
On-site 4 days/week in Sleepy Hollow NY or Warren NJ
If based in Warren NJ occasional travel to Sleepy Hollow NY is expected
Travel (up to 10% is expected)
A typical day may include the following:
Develop and deliver high-quality balanced and scientifically accurate responses to medical inquiries; resolve complex and brought up inquiries.
Lead the creation and maintenance of deliverables including literature reviews Standard Response Documents (SRDs) verbal FAQs Q&As AMCP dossiers and compendium.
Medical reviewer on Promotional and Medical Review Committees ensuring medical accuracy clarity and compliance.
Own department reporting processes and dashboards including metrics insights generation digital analytics and trend reporting for internal partners.
Evaluate pilot and implement AI-enabled tools and technologies to streamline medical information processes and improve efficiency and quality.
Collaborate with global and regional Medical Affairs partners to ensure alignment and share best practices.
Provide scientific support for congress planning booth activities and real-time scientific exchange.
Mentor and train new hires and less experienced colleagues; may directly supervise Senior Managers Specialists and contractors.
To be considered a minimum of 5 years of Medical Information experience within the pharmaceutical industry along with a PharmD or PhD is required. Strong scientific knowledge and expertise in a therapeutic area including evaluating and communicating clinical trial and disease state information to a wide range of audiences. Neurology is preferred. Demonstrated experience in conducting scientific literature review and management of medical inquiries including the development and review of deliverables (e.g. standard response documents FAQs dossier compendium submissions etc.). Practical experience and knowledge of FDA guidances.
Does this sound like you Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits which vary by the U.S. benefits may include health and wellness programs (including medical dental vision life and disability insurance) fitness centers 401(k) company match family support benefits equity awards annual bonuses paid time off and paid leaves (e.g. military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US please visit For other countries specific benefits please speak to your recruiter.
Please be advised that at Regeneron we believe we are most successful and work best when we are together. For that reason many of Regenerons roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regenerons on-site policy and expectations for your role and your location.
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 Companys 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.
Salary Range (annually)
Required Experience:
Director
About Company
Discover how Regeneron (NASDAQ: REGN) harmonizes biology and technology to create life-changing medicines. Join our team and explore clinical trials.
