Syneos Health

HQ
Raleigh
Total Offices: 8
22,543 Total Employees

Syneos Health Benefits Overview

Compensation + Benefits

Offers 401(K)

Offers life insurance

Offers supplemental life insurance

Offers accidental death & dismemberment insurance

Offers disability insurance

Provides a pension

Offers occupational accident insurance

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)

Provides family medical leave

Offers generous parental leave

Work-Life Balance + Wellbeing

Offers company-sponsored outings

Offers an Employee Assistance Program (EAP)

Offers generous PTO

Provides paid sick days

Offers unpaid extended leave

Provides paid holidays

Provides bereavement leave

Career Growth + Development

Provides customized development tracks

Job training & conferences

Company Culture

Utilizes a flexible work schedule

Offers a remote work program

Offers diversity-based Employee Resource Groups

Offers legal assistance

Recently posted jobs

Healthtech • Biotech • Pharmaceutical
Leads end-to-end clinical trial supply planning, forecasting, inventory management, packaging, labeling, distribution, vendor oversight, and risk mitigation. Collaborates with clinical, project management, procurement, and supply chain teams to align supply strategies with study needs. Manages budgets, documentation, reporting, inspection readiness, process improvement, training, and junior staff oversight. Supports business development through bid defenses and client presentations while ensuring compliance with GCP, GMP, ICH, SOPs, and regulatory requirements.
Healthtech • Biotech • Pharmaceutical
Leads statistical programming for compounds, studies, and submission projects using SAS and CDISC standards. Maintains study timelines and programming standards, reviews macros, datasets, validation outputs, and electronic submission documentation. Coordinates programming resources, supports study setup, ensures production-area organization, and mentors junior programmers. Provides expert recommendations and solutions for complex programming and regulatory compliance challenges.
Healthtech • Biotech • Pharmaceutical
Manages clinical study files, databases, regulatory documents, trial metrics, financial reports, meeting actions, document archiving, audit support, and quality activities. Maintains KPIs and customer status reports, supports sponsor communications, and may mentor Project Specialists. Requires Veeva Clinical and Excel proficiency, clinical research and oncology experience, knowledge of GCP/ICH and applicable regulations, strong organization and communication skills, and the ability to work independently while meeting multiple deadlines.