Parexel - Remote work

Join Parexel FSP as a Junior Clinical Trial Manager in a home-based role in Spain. You will manage clinical trials, oversee vendors, and ensure GCP compliance. This role offers exceptional financial rewards and development while dedicated to a single sponsor. Utilize your CRA experience in a posi...

Join Parexel Consulting as a Senior Regulatory Affairs Associate in India. Utilize your expertise in Biologicals, Vaccines, and small/large molecules to develop global regulatory strategies for US, EU, and other key markets. You will prepare and review Marketing Authorization Applications, enjoyi...

Join Parexel Consulting as a Regulatory Affairs Generalist in the UK. Use your scientific degree and regulatory experience to help biopharmaceutical clients navigate complex requirements. You will manage submissions, lifecycle maintenance, and health authority interactions. Enjoy flexible work, c...

Join Parexel as a Senior Clinical Research Associate (CRA) in the Paris Region. You will ensure data integrity and ICH-GCP compliance at investigator sites, working on global projects across diverse therapeutic areas. We seek a professional with a relevant degree, excellent communication skills, ...

Join Parexel as a Regulatory CMC Project Manager. Utilize your 3+ years of CMC regulatory experience to manage complex submissions and strategic plans for biopharma clients. Enjoy a fully remote role with East Coast hours, career growth, and expert mentorship. Be part of a supportive team shaping...

Join Parexel in Taiwan as a Clinical Research Associate (CRA). You will ensure patient safety and protocol adherence at investigator sites, managing global projects across diverse therapeutic areas. The role requires fluency in Japanese and Mandarin, plus strong site management skills. We offer f...

Seeking a Senior Integration Engineer in India with 7+ years of software engineering experience. This role requires deep expertise in MuleSoft 4, API-led connectivity, and designing SOAP/REST services. You will develop high-quality integrations, follow DevOps practices, and collaborate with globa...

Join Parexel as a Veeva Clinical Digital Systems Analyst in Poland. You will optimize clinical trial processes by managing digital systems, bridging technology and operations. This role requires 5+ years in clinical technology and offers a performance bonus, career development, and a friendly wor...

Join Parexel Consulting as a Health Economics Consultant in the UK. Utilize your advanced degree and 3+ years of industry experience in health economics and statistics. You will design evidence-generation strategies and conduct analyses using R/GitLab to support market access. Enjoy flexible work...

Join Parexel as a Senior Clinical Research Associate (CRA) in the UK. You will ensure protocol and ICH-GCP compliance, with recent oncology experience being essential. This role offers flexible work arrangements, career development, and exposure to diverse global therapeutic projects. Build key r...

Lead MAA submissions and regulatory strategy for biopharma clients in this remote project leadership role. Leverage your extensive Regulatory Affairs and CRO experience to manage global filings and ensure client success. Enjoy a flexible work environment with career growth and mentorship from ind...

Join Parexel as a Senior Statistical Programmer to analyze clinical trial data and accelerate new treatments to patients. Utilize your 5+ years of SAS programming and CDISC expertise in a fully remote role across Serbia or Poland. Enjoy a flexible environment with extensive training, career growt...