Parexel

HQ
Raleigh
Total Offices: 9
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

Clinical Trial Manager - FSP

11 Hours AgoSaved
Remote
United States
Pharmaceutical
Manages global clinical trial operations from protocol design through study closeout, including CRO and vendor oversight, regulatory tracking, recruitment, budgets, timelines, risk mitigation, trial documentation, training, and stakeholder coordination. Supports inspection readiness, process improvement, team onboarding, and operational strategy across Phase I-IV studies.
Pharmaceutical
Provides CMC regulatory strategy and post-approval support for biologics and plasma products. Develops submission plans, assesses manufacturing and quality changes, reviews technical documentation, coordinates global regulatory submissions, manages regulatory information systems, and mitigates compliance risks. Requires pharmaceutical regulatory affairs experience, biologics CMC expertise, and knowledge of global post-approval requirements.
Pharmaceutical
Provides operational and administrative support for clinical trials from study start-up through closeout. Responsibilities include maintaining tracking systems and study files, coordinating training and meetings, managing sample and supply tracking, supporting vendors and study teams, performing document quality checks, archiving in the TMF, and assisting with budget tracking. Requires knowledge of clinical operations, ICH-GCP, eTMF systems, and essential trial documents.
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