Remote Jobs at Parexel
Find your next remote opportunity · 103 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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Senior Clinical Database Programmer
Senior Clinical Database Programmer responsible for programming high-quality clinical databases at Parexel. Collaborating with study teams and mentoring junior staff on database technologies.

Manager, Centralized Data & Sample Management – FSP
Manager, Centralized Data and Sample Management overseeing data transfers for studies at Parexel. Contributing to growth of Clinical Data Operations Team while working remotely from Poland, South Africa, or the UK.

Senior Clinical Research Associate – Oncology
Senior Clinical Research Associate managing site monitoring and clinical trial execution in Canada. Ensuring compliance with good practices and regulations during clinical studies.

Senior Director, D&T Operations Support
Senior Director of D&T Operations Support leading global operations support in clinical and safety systems. Overseeing support, reliability, and collaboration with cross-functional teams in biopharmaceutical.

Regulatory Affairs Consultant – Global Labeling Lead
Regulatory Affairs Consultant focusing on global labeling strategies in pharmaceutical development. Collaborating with cross-functional teams to ensure compliance and quality in labeling documentation.

CMC Regulatory Affairs Consultant, Peptides and Oligonucleotides
Regulatory Affairs Consultant leading CMC strategy for peptide and oligonucleotide therapeutics. Collaborating with global teams to ensure compliance and accelerate product approvals.

Vice President, AI Enablement
Vice President leading AI Enablement to implement enterprise-wide AI strategy at Parexel. Overseeing AI governance, platform enablement, and talent development within the Data & Technology organization.

Executive Director – Data & Technology
Executive Director leading technology and data for global Site & Study Startup at Parexel. Driving innovations and operational excellence in clinical trial processes across the organization.

Executive Director, Data & Technology – Clinical Operations
Executive Director overseeing technology and data functions for clinical operations. Leading systems, integrations, and operational enablement in a remote setting.

Regulatory Affairs Associate
Regulatory Affairs Associate coordinating global regulatory submissions for Parexel. Managing submissions and ensuring compliance with regulatory requirements while collaborating with cross-functional teams.

Clinical Research Associate, APEX
Clinical Research Associate focusing on Rare Diseases or Oncology at Parexel. Provide foundational training, support CRAs, and manage site relationships with significant travel expectations.

Global Clinical Trial Lead – Senior Clinical Trial Manager
Global Clinical Trial Lead managing international clinical trial projects for Parexel. Ensuring compliance, stakeholder communication, and trial success across multiple locations.

Principal RWD Strategy Lead
Principal RWD Strategy Lead at Parexel leading real-world data strategy in clinical development across multiple European locations.

Clinical Research Associate I – II
Clinical Research Associate managing clinical trial sites in Australia. Ensuring compliance with protocols and building relationships with site staff.

Senior Clinical Research Associate – FSP
Senior Clinical Research Associate at Parexel managing monitoring responsibilities and site conduct for clinical trials in the healthcare sector. Ensuring compliance with regulations and timelines while partnering with investigator sites.

Regulatory Affairs Consultant
Regulatory Affairs Consultant ensuring compliance in clinical development processes at Parexel. Managing and preparing regulatory submissions for various markets including US, EU, and Japan.

Executive Director, Patient Safety
Executive Director overseeing the Patient Safety pillar at Parexel. Leading management and operational strategies while ensuring compliance and quality in deliverables.

Clinical Operations Manager – Budgets and Contracts
Clinical Operations Manager responsible for managing clinical trial deliverables and compliance within country protocols. Collaborating with teams to ensure successful trial execution and submission.

Senior Clinical Research Associate, Oncology
Senior Clinical Research Associate focusing on oncology studies and ensuring compliance with guidelines. Collaborating with study teams to manage clinical trials efficiently and effectively.