Sr Sample Management Specialist (Study Lead)

Regeneron’s Sample Management Group, located in Tarrytown, NY, is seeking a highly motivated Senior Specialist to manage sample data processes and biobanking operations for Oncology clinical studies and research initiatives. Responsible for leading clinical oncology studies, we believe there is a lot of opportunity to lead in this growing group. This role requires critical thinking, scientific curiosity, attention to detail and drive for results within a team dynamic.

A TYPICAL DAY IN THIS ROLE LOOKS LIKE:

• Responsible for the interpretation of clinical/non-clinical study protocols and associated study documentation as it pertains to biospecimen management. Independently executes study reference file creation by interpreting protocols and other applicable data inputs.

• Manages biosample operations for assigned clinical/non-clinical studies to ensure company deliverables are met.

• Manages the execution of reconciliation and data cleaning of biospecimens to drive deliverables forward.

• Collaborates with Data Management to draft and review Data Transfer Specifications

• Liaises with Global Clinical Development and Central Laboratories to provide input, planning, and integration of biosample operations and data transfers.

• Independently assigns and coordinates sample management activities for assigned programs to support high demand tasks

• Independently handles high priority and high volume tasks within the appropriate timeframe while maintaining accuracy.  Operates effectively in ambiguous and complex situations. Anticipates changing priorities and initiates actions with the appropriate parties.

• Facilitates data reporting needs for clinical/non-clinical/research study queries surrounding sample inventory.

• Works closely with Quality Control (QC) to address findings and ensure data is captured appropriately in LIMS.

• Maintains effective verbal and written communication both internally and with external collaborators and vendors. Communicates with CRO’s and third-party vendors to support sample management responsibilities.

• Ensures compliance and proper documentation in accordance with working instructions, SOPs, and applicable regulations.

THIS ROLE MAY BE FOR YOU IF YOU HAVE:

• Critical thinking skills to interpret scientifically complex information

• Scientifically curious with a passion to drive forward clinical development of oncology products

• Attention to detail when reviewing complex documents

• Drive for results in a high paced and evolving environment

• Previous project management experience

• Enjoys a team dynamic

• Routinely demonstrates sound decision-making ability and incorporates new processes and initiatives within the team.

• Possesses the ability to manage multiple projects simultaneously

• Works collaboratively with other departmental teams/individuals to implement cross-functional initiatives or process improvements.

TO BE CONSIDERED TO BE QUALIFIED FOR THIS ROLE:

• You must have earned a minimum of a bachelor's with 6+ years of relevant laboratory experience.

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 u