Associate Manager Clinical Study

This role is a hybrid position which means the individual must work on-site 3 days per week. Fully remote work is not possible for this role. The position can be based in Armonk, NY, Basking Ridge, NJ or Uxbridge, England.

The Assoc Mgr Clinical Study (CSAM) role supports the Clinical Study Lead (CSL) by taking responsibility for areas of clinical trial delivery. This role applies to internally sourced studies and studies out- sourced to Clinical Research Organizations (CROs) and the balance of direct execution versus oversight of CROs deliverables will vary accordingly. The Assoc Mgr Clinical Study works with the study team internally and externally with vendors such as CROs in feasibility, planning, initiation, maintenance and closeout of clinical projects according to GCP, ICH, CFR and Regeneron Standard Operating Procedures (SOPs). Travel to study sites may be required to assist with monitoring clinical studies.

A Typical Day As a CSAM Looks Like

May lead/oversee the planning and management of a clinical study in an assigned region(s) in alignment with the global study plans and may contribute to global planning and management of the studyContributes to risk assessment and helps identify risk mitigation strategiesSupports feasibility assessment to select relevant regions and countries Oversees and provides input to the development of study specific documentation including but not limited to: case report form (CRF), data management plan, monitoring plan, monitoring oversight plan, etc.Reviews site level informed consents and other patient-facing study start-up materialsOversees setting up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS) and Trial Master File (TMF)Contributes to investigator meeting preparation and executionOversees engagement, contracting and management of required vendors for the studyOversees and provides input to study drug and clinical supplies forecasting, drug accountability and drug reconciliationProvides regular status reports to stakeholders as requested by the Clinical Study LeadContributes to development of and oversees implementation of recruitment and retention strategiesMonitors recruitment and retentionMonitors progress for site activation and monitoring visitsSupports data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations and suspected non-compliance by sitesEscalates data flow and data quality issues to Clinical Study LeadOversees the execution of the specific clinical study deliverables against planned timelinesEscalates issues related to timelines or budget to Clinical Study LeadSupports accurate budget management and scope changesContributes to clinical project audit and inspection readiness throughout the study lifecycleSupports internal and external inspection activities and contributes to CAPAs as requiredManages aspects of study close-out activities including but not limited to database lock, reconciliation of vendor contract, study budget, TMF and study drug accountabilityMay be responsible for mentoring clinical trial management staffMay be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring

This Role May Be For You If

You are an excellent communicator with strong interpersonal skills, and capacity to establish relationships internally and externallyYou have a data driven approach to executing and problem solvingYou have a good attention to detail to deliver on specific study activitiesYou are proactive and self-disciplined, and an ability to meet deadlines with an effective use of timeYou have budget awareness with the ability to get involved in various aspects of budget management

To be considered for this role you must have a Bachelor’s degree and 4+ years’ pharmaceutical industry related work experience. Less experience with an advanced degree may be considered. We must have candidates who have vendor management experience, as well as experience in clinical trial operations including developing key study documents. We also require someone who has technical proficiency in trial management systems, Microsoft applications and TMF, as well as familiarity with medical terms, and a knowledge of Good Clinical Practice and regulatory guidelines.

Up to 25% travel may be required.

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)

$106,200.00 - $173,200.00