Bristol Myers Squibb

HQ
New York
Total Offices: 14
40,384 Total Employees

Bristol Myers Squibb Benefits Overview

Compensation + Benefits

Offers 401(K)

Offers life insurance

Offers supplemental life insurance

Offers accidental death & dismemberment insurance

Offers disability insurance

Offers charitable contribution matching

Offers occupational accident insurance

Offers retiree health & medical

Provides adoption assistance

Provides family medical leave

Provides fertility benefits

Offers childcare benefits

Offers generous parental leave

Offers company equity

Offers employee discounts

Offers performance bonuses

Offers dental insurance

Offers health insurance

Offers mental health benefits

Offers dependent care

Offers Flexible Spending Account (FSA)

Offers vision insurance

Offers Health Savings Account (HSA)

Work-Life Balance + Wellbeing

Offers company-sponsored outings

Offers gym membership

Offers an Employee Assistance Program (EAP)

Offers generous PTO

Provides paid holidays

Provides bereavement leave

Offers unpaid extended leave

Offers paid volunteer time

Provides paid sick days

Provides military leave

Career Growth + Development

Provides customized development tracks

Job training & conferences

Provides tuition assistance

Company Culture

Utilizes a flexible work schedule

Offers a remote work program

Offers diversity-based Employee Resource Groups

Provides a mobile phone discount

Offers legal assistance

Healthtech
Leads clinical supply chain and planning for domestic and international clinical trial product fulfillment. Oversees labeling, packaging, distribution, procurement, vendor and depot relationships, inventory, warehousing, compliance, risk management, and cost optimization. Establishes clinical supply chain teams and processes while partnering with manufacturing, quality, regulatory, finance, and commercial stakeholders. Manages team development, succession planning, and adherence to cGMP, GDP, FDA, and DOT requirements.
Healthtech
Supports clinical trial operations by managing study vendors, CRO activities, budgets, documentation, timelines, risk mitigation, and performance metrics. Assists with protocol and study document reviews, country and site start-up, site feasibility, issue resolution, and Trial Master File quality. The role requires compliance with SOPs, FDA regulations, ICH/GCP guidelines, and study timelines. Up to 10% travel is required.
Healthtech
Manages clinical study vendors and supports CRO, site, and study execution activities in compliance with SOPs, FDA regulations, and ICH/GCP guidelines. Responsibilities include vendor planning, performance tracking, risk mitigation, budgets, invoicing, study start-up, site feasibility, documentation, TMF quality, and escalation of operational issues. The role requires cross-functional collaboration and up to 10% travel.