The Clinical Supply Operations Specialist provides support to the Clinical Drug Supply Logistics group in the Investigational Product (IP) distribution process, and ancillary supplies process, for one or more molecules across multiple Therapeutic areas supporting moderately complex studies as well as short-term departmental projects and ongoing continuous improvement initiatives. Activities are performed on time, within budget and with good quality, in compliance with Regulatory Authorities’ regulations / guidelines and Regeneron Standard Operating Procedures (SOPs) / Work Practice Documents (WPDs). This role applies to internally sourced studies and/or CRO/Partnered studies

A typical day might include the following:

Solving complex problems, and initiate completion of the following items within broadly defined practices and policies including selecting methods, techniques, and evaluation criteria for obtaining results related to:

IP Supply Inventory Planning

IP Shipments

IP Supply Monitoring Activity Documentation (Electronic Trial Master File - eTMF)

Ancillary Supply Inventory Planning/Management

Comparator Planning Management

Financial Forecasting, Budgeting Planning

This role might be for you if:

You have foundational knowledge of the clinical drug development process and clinical trial methodology including the inner-workings of cross-functional partners

You are knowledgable of International Council of Harmonization (ICH) / Good Clinical Practices (GCP) regulatory guidelines/directives

You are Proficient in MS Word Excel

You can come up with solutions and work in ambiguity

To be considered for this opportunity, we expect you to have 2years of experience in the life sciences within Clinical Supplies, Regulatory, Quality, Manufacturing or Supply chain. We are also expecting you to have a bachelor's degree. Lastly, we require you to be in our office a few days a week.

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.

Salary Range (annually)

$69,300.00 - $112,900.00