At Regeneron, our medical affairs physicians and scientists are at the forefront of innovation, playing a crucial role in our global development organization. As a key liaison between Regeneron and the scientific and healthcare community, you will be part of an optimally aligned matrix structure delivering therapeutic and functional area expertise in our Oncology division.

You will engage in scientific exchange and collaborate with therapeutic area experts on disease and product information as well as research initiatives. You will present scientific data, clinical data, and disease state awareness in response to requests for information to diverse audiences (therapeutic area experts, practitioners, investigators, research coordinators, site personnel and internal stakeholders).

A typical day might include:

Identifying and maintaining a list of relevant medical/therapeutic area experts, investigator targets, and associated plans of action.

Responding to requests for information related to study indications, disease state, and therapeutic area, and presenting/discussing scientific and clinical data to the appropriate audience in a compliant manner.

Performing disease management and therapeutic area education with identified practitioners, payers, and researchers.

Attending medical conferences to collect and report relevant scientific, clinical, and competitive intelligence to inform internal stakeholders.

Assisting with the management of clinical data to ensure rapid and accurate communication of scientific/clinical results through support of abstract, poster, presentation, and manuscript development.

Establishing scientific relationships with investigators and internal Medical Affairs to support the investigator-initiated study (IIS) program.

Identifying gaps in research needs, especially related to the Japan/Asia environment, and creating opportunities to fill those gaps by collaborating with potential and existing investigators.

Supporting the development program if requested by Clinical Development and Clinical Operations.

Acting as a scientific resource for area healthcare professionals within the surrounding trial site community.

Collaborating with Clinical Development, Clinical Operation, and other trial staff to execute plans and strategies established by Medical Affairs.

Helping to identify and assist in the selection of investigators and trial sites.

Formulating appropriate rules and procedures for MSL activities at Regeneron Japan to comply with relevant laws, regulations, guidelines, policies, and industry rules, especially during the expansion phase.

This role might be for you if:

You're an experienced healthcare or scientific professional with a strong academic track record, a background in oncology medical affairs, exceptional communication skills, and a collaborative mindset. You are patient-focused, compliance-oriented, adaptable, and capable of identifying and addressing research gaps.

To be considered for this position, you possess a PhD, MD, PharmD qualification with oncology experience and/or clinical trial experience. Additionally, you have deep knowledge and significant experience in the field of lung cancer and ideally, experience in immuno-oncology. You have demonstrated experience in the pharmaceutical industry or clinical settings, such as drug information, disease management programs, or clinical pharmacy/medicine and you are able to travel 30-50% of the time if required. In our global matrix organization, we expect fluency in both Japanese and English languages to facilitate cross-functional and truly international collaboration. ​

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.