This is a hybrid a role on-site 3 non-consecutive days inclusive of a Monday or Friday, and 2 days from home each week. A fully remote role is not possible for this role.

The Clinical Study Assistant (CSA) in Clinical Trial Managementis responsible for supporting the clinical study team(s) members in the initiation, maintenance, and closeout of clinical trials according to Good Clinical Practice (GCP), International Conference for Harmonization (ICH), Code of Federal Regulations (CFR) and Regeneron Standard Operating Procedures (SOP).  The CSA assists the Clinical Study Lead and/or other clinical study team with all aspects of study execution. 

In a typical day you will:

Be a key study team member responsible for multiple clinical trials (all phases) and assure compliance with SOPs, FDA regulations, GCP and ICH guidelinesParticipate in Clinical Study team meetings for one or more clinical studiesAssist in the writing, collection, distribution and filing of meeting agenda and meeting minutesSuppor the scheduling and coordination of team meetings and minutesDistribute materials to study sites, as directedAssist with requesting, collecting, and reviewing site regulatory documents Track site study start up status and activities using established study toolsReview, maintain, and reconcile (QC) essential study documents and electronic Trial Master File (eTMF) according to TMF planSupport and participate in tracking organization and maintenance of study reporting tools such as monitoring visit schedulesCollate and assemble study documents under guidance of the study specialist or study manager for: study binders (regulatory, pharmacy, laboratory), study reference manuals, CRA training and Investigator Meeting materials, and study data collection toolsMaintain team document repositories and/or shared drive sites as neededAssist or drive the submission process for internal review committees (e.g., Clinical Review Committee) and may attend review meetings on behalf of the study teamRequest and track Clinical Disclosure Agreements (CDA) and consulting agreementsMay assist with study related tasks including reviewing monitoring visit reports and providing feedback to the CSL, supporting the quality notification process, and data review process.Ensure scheduled reports are received, reviewed and actioned (i.e. FDA Form 1572 reportable changes, financial disclosure form status)Track and monitor study close out activities – including study close-out documents (FDA Form 1572s, Investigational Product reconciliation, Financial Disclosures, etc.) and Clinical Research Associate (CRA) close-out visitsMay require 25% travel

To be considered you must have:

0-1 year experience (Entry Level), Bachelor’s degree preferred, Associates Degree may be accepted.  Preference to candidates with a life science or nursing degreeGeneral understanding of the clinical research process and regulations/guidelinesRegularly contributes useful ideas for own work area/team, within defined parametersEffective communication and interpersonal skills; ability to build relationships internally and externally, as requiredFamiliarity with medical terminologyProficiency with Microsoft Office applications, Excel and PowerPointGood time management, ability to prioritizeEffective written and verbal communication skillsAttention to detail and accuracy of workComfortable multi-tasking in a fast-paced environment and able to adjust workload based upon changing prioritiesEscalates non-routine matters and complex problems, as needed

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 (hourly)

$33.94 - $55.38