Key Facts

Remote From:

Brazil , Argentina , Mexico , Canada , South America , United States

Full time

English

Hard Skills

Patient Safety Healthcare Industry Knowledge Regulatory Compliance Regulatory Compliance Regulatory Compliance Regulatory Compliance Industry Trend Analysis Digital File Management Event Tracking Regulatory Compliance +10 more

Other Skills

•
Empathy
•
Physical Flexibility

Roles & Responsibilities

Interest and background in regulatory affairs or patient safety with a passion for advancing global health
Ability to work remotely from home and collaborate with global teams while maintaining work-life balance
Familiarity with regulatory lifecycle components such as labeling, labeling strategy, advertising and promotion, CMC, and publishing
Experience with or understanding of global health authorities and navigating international regulatory submissions

Requirements:

Support regulatory submissions and document publishing to ensure timely delivery of compliant dossiers
Assist with labeling operations and labeling strategy to ensure accurate, compliant product information
Support patient safety activities by identifying risks, monitoring safety events, and documenting and tracking events
Collaborate with cross-functional teams and health authorities to navigate regulatory requirements and promote patient safety throughout development

Parexel

Pharmaceuticals

About Parexel

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.

Company type: XLarge

Industry: Pharmaceuticals

Founded: 2018

Company size: 10001

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Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Explore Your Next Chapter in Regulatory Affairs or Patient Safety

At Parexel, we value the expertise and dedication of regulatory and patient safety professionals who are passionate about advancing global health. This career page highlights opportunities where your skills can make a meaningful impact in shaping the future of drug development.

We also recognize the importance of flexibility in how you work. Our Regulatory Affairs and Patient Safety opportunities offer the ability to work remotely from home, empowering you to contribute globally while maintaining balance in your personal and professional life.

Regulatory Affairs is a diverse and dynamic field, offering pathways for specialists across multiple disciplines:

Labeling Operations – ensuring accuracy and compliance in product information.
Labeling Strategy – shaping global labeling approaches to meet evolving regulatory requirements.
Advertising & Promotion – guiding compliant communications that balance innovation with patient safety.
Chemistry, Manufacturing, and Controls (CMC) – driving product quality and development through technical and regulatory expertise.
Regional and Global Health Authority Expertise – leveraging direct experience with agencies worldwide to navigate complex approval processes.
Regulatory Operations & Publishing – managing submission processes, document publishing, and ensuring timely delivery of compliant dossiers.

Patient Safety roles support Parexel's commitment to delivering safe, high‑quality care by identifying risks, monitoring safety events, and promoting continuous process improvement.

Patient Safety Associate - supporting the review, documentation, and tracking of patient safety events and assisting in analyzing trends and risks

If you are interested in learning more, we invite you to express your interest in joining Parexel. Explore the opportunities available and discover how your expertise can help us deliver solutions that improve patients’ lives worldwide.

EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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