Parexel

HQ
Raleigh
Total Offices: 9
20,524 Total Employees

Parexel Benefits Overview

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

2 Days AgoSaved
Remote
United States
Pharmaceutical
Supports clinical and scientific conduct of clinical studies, including adjudication, medical monitoring, imaging data reconciliation, meeting materials, protocol deviation management, and study data review. The role may support multiple studies, interact with study sites and committees, and lead limited-scope studies. Responsibilities also include resolving data discrepancies, reviewing patient and medical record information, maintaining compliance with ICH-GCP and company processes, and completing required administrative tasks.
2 Days AgoSaved
Remote
2 Locations
Pharmaceutical
Manages clinical trial sites throughout study phases, serving as the primary site contact. Conducts remote and on-site monitoring, verifies data quality and participant safety, manages regulatory documentation, supports site activation and closeout, resolves compliance and performance issues, and maintains trial systems. Collaborates with investigators, sponsors, and cross-functional teams while supporting audits, inspections, mentoring, and study deliverables. Requires extensive domestic and international travel.
Pharmaceutical
Conducts qualification, initiation, monitoring, and termination visits for clinical trial sites. Manages site quality, performance, regulatory documentation, data integrity, investigational product accountability, enrollment support, and compliance with protocols, Good Clinical Practice, SOPs, and regulations. Serves as the primary contact for investigators and site teams, resolving issues and safeguarding participant safety across oncology, ophthalmology, metabolic, hematology, or CAR-T studies.