Senior Specialist, Clinical Supply Operations

The Senior Specialist, Clinical Supply Operations provides support to the Clinical Drug Supply & Logistics (CDSL) group in the Investigational Product (IP) distribution process, ancillary supplies process, and comparator procurement process, for one or more molecules across multiple Therapeutic areas supporting highly sophisticated studies as well as long-term departmental and cross-functional projects and ongoing continuous improvement initiatives. They may lead short-term projects. 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:

• Taking on sophisticated problems, and initiate completion of the following items within broadly defined practices and policies including selecting methods, techniques, and evaluation criteria for acquiring results related to IP Supply & Inventory Planning, Ancillary Supply & Inventory Planning/Management, Comparator Planning & Management, and Financial Forecasting, Budgeting & Planning.

• Resolving objectives of assignment and be able to plan schedules and arrange own activities in accomplishing objectives.

• Representing CDSL as a prime contact on contracts or projects.

• Interacting with senior internal and external personnel on significant matters, often requiring coordination between organizations.

This role might be for you if:

• You have a strong understanding of the clinical drug development process and clinical trial methodology including the inner-workings of cross-functional partners.

• You have knowledge of International Council of Harmonization (ICH) / Good Clinical Practices (GCP) & regulatory guidelines/directives.

• You are an efficient problem solver.

• You have a strong instinct to act and adaptable.

To be considered for this opportunity you must have at minimum 3+ years of experience in a supply chain role. Experience working with clinical trials is a highly preferred. This is a hybrid role, requiring you to come on-site 2 times a week, with 3 days work-from-home.

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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)

$79,000.00 - $129,000.00