Remote Jobs at Parexel

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Parexel

Pharmaceutical Manufacturing

Healthcare InsuranceBiotechnologyPharmaceuticals

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. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

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2d

Principal Medical Writer, FSP

Parexel

Principal Medical Writer at Parexel FSP producing and editing clinical/regulatory submission documents. Ensuring ICH, GCP and Sponsor SOP compliance while managing timelines.

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2d

Senior Clinical Data Analyst

Parexel

Lead data management for Phase I–IV clinical trials at Parexel; design eCRFs, manage EDC, mentor staff, liaise with CROs

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2d

Medical Communications Program Specialist, Oncology Publications

Parexel

Program Specialist coordinating oncology publications and cross-functional teams at Parexel, a global clinical research organization.

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3d

Senior Clinical Research Associate

Parexel

Home-based Senior CRA managing oncology site monitoring for Parexel's clinical trials in Poland. Responsible for site management, supervisory activities, mentoring, and ensuring GCP-compliant study conduct.

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