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As an Associate Director, Field Medical Affairs you will engage in scientific exchange and collaborate with Oncology disease experts and product information as well as research initiatives. We provide Oncology scientific and/or medical expertise and serves as a scientific/medical resource. We accomplish this by presenting scientific data, clinical data and disease state awareness in response to requests for information to therapeutic area specialists, practitioners, investigators, research coordinators, site personnel and internal partners.
This is a field-based position and requires work in a multifunctional, matrix organization and possibly partner companies. This job will be supporting Texas, Oklahoma, Arizona, and Louisiana.
A typical day may include the following
Identifies and maintains a list of relevant medical/therapeutic area professionals, investigator targets and associated plans of action.
Participates in the development and management of company sponsored clinical trials including:
Review of concept proposals and development of protocols
Identifies and assists in selection of investigators and trial sites
Supports site initiation and enrollment activities
Acts as a scientific resource for area healthcare professionals within the surrounding trial site community
Collaborates with Clinical Development and other trial staff to implement plans and strategies established by Medical Affairs
Establishing scientific relationship with investigators and internal Medical Affairs, supports investigator-initiated study (IIS) concept program.
Identifies gaps in research needs of company and creates opportunities to fill those gaps by collaborating with potential and existing investigators and site personnel.
Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific and clinical data to appropriate audience in a compliant manner.
Performs disease education with identified practitioners, payers and researchers.
Attends medical conferences to collect and report relevant, scientific, clinical, & competitive intelligence with the purpose of informing internal partners.
Assists with management of clinical data to ensure rapid and accurate communication of scientific/clinical results through support of abstract, poster, presentation, and manuscript development.
This may be for you if:
Enjoy working independently in the field, while having an impact on the company’s mission.
Are passionate about developing knowledge of and sharing clinical scientific data
Like working corroboratively and developing relationships in academic and clinical practice settings
Have the highly developed ability to balance multiple initiatives, prioritize them and implement them independently, while excelling at keeping all partners advised and engaged
To be considered for this an advanced Clinical/Science Degree required (MD, PharmD, PhD) is required along with a minimum of 5 years related work experience (clinical, managed care, or industry experience). Oncology experience is required. Experience in a Field Medical or Clinical role is preferred.
Ability to communicate and disseminate scientific and clinical data in response to unsolicited requests for information as appropriate per medical field policy, using oral presentations, written communications, scientific literature or other approved materials and tools.
Residence in assigned territory is required.
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)
$165,900.00 - $270,700.00
Regeneron Pharmaceuticals provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
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