The Associate Medical Director works with supervisor and other members of the cross-functional study team to author early clinical development protocols and facilitate execution of study activities and data summarization. Working with the ECD&ES Disease Area Lead, takes lead on various collaborations with TFA Research and Regeneron Genetic Center (RGC) colleagues to understand current and emerging targets/molecule program, provide input on potential disease areas/indications, and craft clinical experiments that corroborate or inform the biology for decision-making purposes. This position would allow you to work on multiple therapeutic areas such as respiratory, immunology, metabolism, cardiovascular, and other non-oncology areas.
As an Associate Medical Director, a typical day might include the following:
Leads the cross-functional study team Crafts POC-enabling human studies, First-In-Human (FIH) studies, POC (clinical and/or pharmacologic) studies as per strategy
Responsible for the relevance and accuracy of medical science underpinning of clinical study based on detailed scientific review and consultation
Reviews and finalizes the medical and scientific portions of clinical study concepts (CSCs) and clinical study protocols (CSPs) and amendments.
Reviews and edits documents related to trials, such as monitoring plans, SAPs, amendments, IRB/IEC submissions and regulatory submissions
Accountable for timely clinical trial execution and quality of results
Analyzes the benefits and risk aspects of an assigned therapeutic candidate
Ensures Clinical Team compliance with FDA, EMEA, ICH and GCP guidelines as well as SOPs regarding safety
Authors clinical sections of communications/documentation for regulatory agencies and may participate in meetings as needed
Conducts detailed literature reviews and analysis of development opportunities from mechanistic, pharmacological and clinical development perspective
This role might be for you if:
You want to make a broader impact on developing medicines for patients with serious diseases
You have experience in analysis of clinical and basic research information from a wide range of topics
You demonstrate critical thinking skills and sound decision making
You have the ability to work productively in a fast-paced collaborative working environment
To be considered for this position, you must have an MD or MD/PhD with Board Certification or Eligibility in a relevant area preferred as well as 2-3 years of related experience. Experience in clinical research and/or basic science research in an academic setting strongly preferred. We are seeking a strong communicator both written and verbal.
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Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits including health and wellness programs, fitness centers and 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. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.
The salary ranges provided are shown in accordance with U.S. law and apply to U.S. based positions, where the hired candidate will be located in the U.S. If you are outside the U.S, please speak with your recruiter about salaries and benefits in your location.
Salary Range (annually)