TEMP - Clinical Logistics Associate II

Tarrytown, NY, United States
Jan 22, 2021
Required Education
Bachelors Degree
Position Type
The Clinical Logistics Associate II (CLA II) provides support to the Clinical Logistics group and IP distribution process for one or more molecules across multiple Therapeutic areas. You will provide assist in managing clinical drug supply for one or more early phase clinical studies and contributing to ongoing process improvement initiatives. This role applies to internally sourced studies and/or CRO/Partnered studies. We need an individual who can effectively collaborate with clinical trial managers, and staff from quality, clinical compliance, clinical logistics and IOPS.

As a CLA II a typical day might include the following:
  • Preparing systems for inputting and following IP shipments, temperature excursions, and product expiry.
  • Managing investigational product (IP) inventory. Managing orders from shipment through receipt at investigator study sites.
  • Independently initiating IP shipment orders according to supply plans or as requested by Clinical Logistics Manager or Clinical Trial Management team.
  • Communicating with distribution vendors to ensure timely shipment and delivery to investigator sites.
  • Processing, reviewing and evaluating temperature excursion reports from clinical sites and communicating stability information and/or product acceptability.
  • Providing support in reviewing, tracking and/or archiving IP returns documentation.
  • Being responsible for IP expiry data and advising appropriate Clinical Supply and Clinical Trial staff of pending IP expiry.
  • Facilitating ancillary supply shipments and managing in-house inventory.
  • Ensuring appropriate documentation of IP supply activities is provided to clinical trial teams for the Trial Master File.
  • Compiling metrics related to drug supply processes and producing reports on supply status
This role may be for you if:
You have worked with Clinical Study teams and external vendors to act on specific trial needs.
You have experience working with cross-functional clinical groups to provide and receive information required for achievement of individual or team assignments, goals and objectives.
You have solid understanding of clinical logistics systems and processes
You have experience with vendor management.
You have excellent judgment in elevating issues to the appropriate team members for consideration and resolution

To be considered for this opportunity you must have:

To be considered for this role, you must have a Bachelor's Degree and at least three years of relevant clinical supply management experience within the biotechnology/pharmaceutical industry.

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 amazing benefits including health and wellness programs, fitness centers and stock for 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 maternity 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.