Remote Jobs at Parexel
Find your next remote opportunity · 194 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 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 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 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 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.

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 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.

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

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 – 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.

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.

Medical Director, Oncology – GI Subspecialty
Medical Director providing medical monitoring and consultation for oncology clinical trials at Parexel. Collaborating with project teams and regulatory agencies to ensure compliance and safety.

GCP Quality Governance Operations Lead – Senior Manager
GCP Quality Governance Operations Lead at Parexel ensuring robust governance and compliance in clinical trials. Collaborating to enhance quality management practices in pharmaceutical processes.

GCP Quality Governance Operations Lead
GCP Quality Governance Operations Lead managing quality governance forums in pharmaceuticals. Leading initiatives to ensure compliance with GCP regulatory requirements and quality management standards.

Senior Clinical Research Associate - FSP
Overseeing monitoring responsibilities and ensuring proper conduct of clinical trials at Parexel. Collaborating with sites and managing operational aspects of clinical research in South Korea.

Medical Director – Ophthalmology
Medical Director specializing in Ophthalmology for Parexel's Global Medical Sciences team. Leading medical support and client engagement in a remote European role

Senior/Principal Regulatory Compliance Consultant
Senior Regulatory Compliance Consultant providing QC Microbiology expertise to ensure sterile drug product safety. Leading diverse consulting engagements and driving compliance improvements with significant travel requirements.

Senior Regulatory Affairs Associate, Regulatory Intelligence
Senior Regulatory Affairs Associate at Parexel monitoring regulatory developments and providing actionable insights. Engage in industry discussions and collaborate with global teams for compliance excellence.