Remote Jobs at Parexel
Find your next remote opportunity · 140 Open Positions

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster.
Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere.
Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient.
With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference.
For more information, visit parexel.com.
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Project Manager, Early Phase
Project Manager overseeing the sponsor communication and clinical trial management for Parexel in China. Responsible for leading project teams and ensuring study timelines are met.

Site Activation Partner
Site Activation Partner overseeing start-up phase of clinical trials at Parexel. Building relationships with investigators and ensuring compliance with regulatory requirements.

Regulatory Affairs Consultant – Compliance, Process
Regulatory Affairs Consultant focusing on compliance and quality operations in GxP environments for Parexel. Collaborating with cross-functional teams to deliver compliant and efficient business operations.

Senior Vice President, Technical - Clinical Regulatory Affairs
Senior/Vice President, Technical overseeing regulatory strategies for biopharma clinical development. Work from home position with significant impact on patient therapeutic developments.

Associate Director, FSP Clinical Operations / FSP Program Lead
Associate Director managing FSP Clinical Operations for Parexel, a global CRO specializing in clinical research, focusing on improving health outcomes. Overseeing staff and client projects, ensuring quality and timely delivery.

Strategic Proposal Writer
Strategic Proposal Writer at Parexel driving proposal success and managing contract development. Collaborate with leaders to create compelling proposals in a leading Clinical Research Organization.

Clinical Research Associate, Senior - FSP
Clinical Research Associate managing clinical trials at various investigator sites for Parexel. Ensuring patient safety and quality study execution with strong regulatory compliance.

Supply and Logistics Coordinator
Supply & Logistics Coordinator supporting the development and execution of clinical trial supply chain strategies at Parexel. Collaborating on project execution and ensuring compliance with quality standards.

Regulatory Operations Sr. Project Manager, 規制提出プロジェクトマネージャー
Regulatory Operations Sr. Project Manager leading regulatory submission projects for Parexel. Ensure high-quality submissions to authorities within deadlines with collaboration across teams.

Local Study Associate Director – Oncology
Local Study Associate Director managing clinical trials and Local Study Teams for Parexel in Canada. Responsible for site management, study commitments, and ensuring compliance with regulations.

Senior Regulatory Affairs Associate – Clinical Trial Application
Clinical Trial Submission Lead managing and executing Clinical Trial Applications globally. Ensuring compliant submissions across multiple studies with effective team collaboration and stakeholder engagement.

Supply and Logistics Project Manager
Supply & Logistics Project Manager at Parexel leading clinical logistics projects. Ensuring project delivery on time and within budget while maintaining high quality standards and compliance.

Manager, Clinical Operations – Line Manager
Manager overseeing Clinical Operations, responsible for team management and successful project execution at Parexel. Driving clinical research solutions and guiding projects in collaboration.

Human Resources Business Partner – 12 month FTC
Human Resources Business Partner at Parexel supporting global HR initiatives and employee development. Analyzing data and collaborating with business management to improve HR services.

Local Study Associate Director – Oncology
Local Study Associate Director leading Local Study Teams in Oncology clinical trials at Parexel. Ensuring compliance, quality, and timely delivery of study commitments at country level.

Manager, Clinical Operations – FSP
Manager overseeing a team for clinical operations at Parexel, ensuring project deliverables meet quality standards. Responsibilities include resource allocation, staff development, and client management.

Senior Regulatory Consultant – Advertising & Promotion
Senior Regulatory Consultant leading FDA regulatory strategy for advertising and promotion compliance. Collaborating with cross-functional teams to ensure effective healthcare communications while mitigating risk.

Clinical Research Associate I/II
Clinical Research Associate implementing and monitoring clinical trials for Parexel in China. Ensuring compliance with regulatory requirements and effective communication with investigative sites.

FSP Line Manager, Operations Manager
Clinical Operations Manager responsible for oversight of team and project deliverables at Parexel. Requires extensive clinical trial management experience, focusing on quality and timely project delivery.

Senior Director, Events
Senior Director of Events leading the global events strategy for Parexel. Managing high-quality events to drive organizational goals and stakeholder engagement.