Parexel

HQ
Raleigh
Total Offices: 68
20,524 Total Employees
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Parexel Benefits Overview

Compensation + BenefitsWork-Life Balance + WellbeingCareer Growth + DevelopmentCompany Culture

Compensation + Benefits

Offers 401(K)

Offers life insurance

Offers accidental death & dismemberment insurance

Offers disability insurance

Offers supplemental life insurance

Provides adoption assistance

Offers generous parental leave

Provides family medical leave

Provides fertility benefits

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)

Offers employee stock purchase plan

Offers employee discounts

Offers performance bonuses

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 military leave

Provides paid holidays

Provides bereavement leave

Offers unpaid extended 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

Recently posted jobs

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Parexel

Regulatory Affairs Consultant

13 Hours AgoSaved
In-Office or Remote
Hyderabad, Telangana, IND
Pharmaceutical
Support global regulatory lifecycle management across EU, US, and other markets. Develop regulatory strategy, prepare and coordinate global submission packages (Modules 1-5), manage post-approval changes and Health Authority queries, maintain RIM records, support safety reporting, and assist with audit and inspection readiness while tracking submission timelines.
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Parexel

Senior Regulatory Affairs Associate

13 Hours AgoSaved
In-Office or Remote
Raleigh, NC, USA
Pharmaceutical
Support global regulatory lifecycle management and submission activities across EU, US, and other markets. Contribute to regulatory strategy, prepare CTD Modules 1-5, manage post-approval changes and Health Authority queries, maintain RIM records, support safety reporting, and assist with audit, compliance, and inspection readiness.
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Parexel

Clinical Research Associate I/II/Senior-FSP

13 Hours AgoSaved
In-Office
Taipei City, TWN
Pharmaceutical
Serve as primary point of contact for assigned clinical sites across start-up, maintenance, and close-out. Manage feasibility, regulatory submissions, site activation, monitoring (on-site and remote), data quality, TMF maintenance, training, and supply accountability while ensuring ICH-GCP compliance and supporting audits and inspections.
see all jobs at Parexel