Remote Jobs at Parexel
Find your next remote opportunity · 200 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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Clinical Coder – FSP
Clinical Coder responsible for coding clinical trials and ensuring data consistency. Performing medical coding activities for various departments at Parexel, focusing on quality and compliance.

Country Study Operations Manager – France
Country Study Operations Manager responsible for study management in clinical trials at Parexel. Leading study activities and vendor management with a focus on patient well-being.

Data Surveillance Analyst
Data Surveillance Analyst responsible for data analysis and compliance with clinical monitoring at Parexel. Engaging in Data Surveillance Plans and documentation to advance clinical trial processes.

Global Supply Sourcing Coordinator
Global Supply Sourcing Coordinator providing tactical sourcing solutions for clinical trial supplies and managing supplier relationships. Analyzing requirements and advising on sourcing operations.

Clinical Trial Specialist – Associate Clinical Operations Leader
Clinical Trial Specialist supporting clinical studies in a remote capacity at Parexel. Collaborating with clinical teams to ensure adherence to Good Clinical Practices.

Regulatory Affairs Associate
Regulatory Affairs Associate for Parexel developing and publishing regulatory submissions to health authorities. Collaborating with stakeholders to ensure compliance and quality in documentation.

Clinical Project Manager – FSP
Project Manager overseeing planning and execution of clinical study initiatives at Parexel. Collaborating with various teams to ensure project success and timely delivery.

Senior Clinical Research Associate, Clinical Research Associate II
Senior Clinical Research Associate responsible for site management and monitoring of clinical trials across the US. Ensuring compliance and safety while enhancing investigator site relationships in line with GCP standards.

Regulatory Affairs Consultant – CMC, Biological, Vaccines
Regulatory Affairs Consultant handling CMC submissions for biopharmaceutical company. Author global CMC documents and ensure compliance with regulatory requirements across regions.

Regulatory Affairs Associate – Labeling, Marketing Application
Regulatory Affairs Associate managing labeling and ensuring compliance with local regulatory requirements. Supporting marketing authorization submissions and collaborating with various teams to maintain accuracy.

Regulatory Affairs Associate – Labeling VAR Coordination
Regulatory Affairs Associate managing product labeling ensuring compliance with regulatory requirements at Parexel. Supporting marketing authorization submissions and collaborating with cross-functional teams for labeling accuracy.

Regulatory Affairs Consultant – Labelling Strategy
Regulatory Affairs Consultant developing labeling strategies for pharmaceutical products globally. Collaborating with cross-functional teams to ensure compliance and alignment with global regulations.

Regulatory Affairs Consultant – CMC Biologics
Regulatory Affairs Consultant focusing on post-approval regulatory activities for CMC in biological products at Parexel. Requires experience in regulatory affairs within pharmaceuticals and strong CMC knowledge.

CRO Pricing & Contracts Specialist
Pricing & Contracts Specialist at Parexel handling project budgets and contract development. Involves client interactions, budget negotiations, and document finalization tasks.

Senior Data Engineer – Visual Data Analytics Specialist, Spotfire
Senior Data Engineer/Visual Data Analytics Specialist at Parexel creating data visualizations for clinical data analysis with a focus on early development. Home-based position in the UK, Poland, or South Africa.

Medical Director – Ophthalmology
Medical Director in Ophthalmology at Parexel, a global clinical research organization. Providing medical expertise for drug development projects remotely in Europe.

Medical Director – Ophthalmology
Medical Director in Ophthalmology for Parexel, improving health through clinical and consulting solutions in global CRO. Focus on medical monitoring and client engagement.

Senior Data Engineer
Senior Data Engineer creating and maintaining data visualizations for Medical Data Review at Parexel. Supporting safety signal detection while adhering to quality management standards and guidelines.

Data Manager
Data Manager responsible for managing clinical data and improving data processes at Parexel. Collaboration with study teams to deploy digital endpoints in clinical trials.

Senior Data Engineer
Senior Data Engineer creating standardized visualizations to support Medical Data Review at Parexel. Collaborating with teams to enhance safety signal detection and compliance documentation.