Regeneron

Regeneron

HQ
Tarrytown
Total Offices: 8
15,000 Total Employees
Year Founded: 1988

Regeneron Benefits Overview

Compensation + Benefits

Offers 401(K)

Offers life insurance

Offers supplemental life insurance

Offers disability insurance

Offers charitable contribution matching

Offers accidental death & dismemberment insurance

Provides adoption assistance

Provides family medical leave

Offers childcare benefits

Offers generous parental leave

Offers company equity

Offers performance bonuses

Offers employee stock purchase plan

Offers employee discounts

Offers dental insurance

Offers health insurance

Offers mental health benefits

Offers Flexible Spending Account (FSA)

Offers vision insurance

Offers Health Savings Account (HSA)

Company Culture

Provides commuter benefits

Provides a mobile phone discount

Provides free snacks and drinks

Offers legal assistance

Work-Life Balance + Wellbeing

Offers company-sponsored outings

Offers gym membership

Offers an Employee Assistance Program (EAP)

Offers generous PTO

Provides paid sick days

Provides bereavement leave

Provides paid holidays

Offers sabbatical leave

Career Growth + Development

Provides customized development tracks

Job training & conferences

Provides tuition assistance

Recently posted jobs

3 Days AgoSaved
In-Office or Remote
3 Locations
Biotech • Pharmaceutical
As a Director in Quantitative Pharmacology, you oversee PK/PD evaluations, ensure high-quality analyses and reports, and communicate regulatory developments effectively. You need extensive experience in pharmacokinetics, author regulatory documents, and display excellent communication skills. A PhD and 10+ years in the field are required.
5 Days AgoSaved
In-Office or Remote
3 Locations
Biotech • Pharmaceutical
Lead model-informed drug development (MIDD) and pharmacometrics strategies across modalities; deliver population PK/PD, exposure-response, and translational modeling; inform dose selection, trial design, and regulatory strategy; represent QP in program meetings and regulatory interactions; author regulatory documents; mentor junior scientists; implement new modeling approaches and ensure scientific and regulatory quality.
8 Days AgoSaved
In-Office
3 Locations
Biotech • Pharmaceutical
Manage regional clinical study delivery in collaboration with Clinical Study Lead, CROs, and vendors. Oversee study documentation, systems (CTMS, TMF, EDC, IVRS/IWRS), vendor contracting, recruitment/retention, data quality, budgeting, timelines, and close-out activities while ensuring ICH/GCP and inspection readiness.