Parexel - Research and Development

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. Use your scientific degree and industry experience to develop strategies for biopharma and medical device clients. Manage submissions, lifecycle maintenance, and health authority interactions in a flexible, supportive global environment.

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 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...

Join our team as a Scientist III - Analytical Chemist on the third shift in Rahway, NJ. This role requires hands-on experience with HPLC, GC, and wet chemistry methods within a cGMP environment. You will operate and maintain analytical instrumentation, ensuring high-quality, compliant results. We...

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 Clinical Research Associate (CRA) in the United States. You will ensure trial conduct and patient safety, monitoring sites with 60-80% travel. Requires 3+ years monitoring experience, ICH/GCP knowledge, and fluency in English. Work on global projects with career growth in...

Join Parexel's Biostatistics team in Taiwan to support new treatment efficacy and safety. Utilize your statistical expertise in clinical trials, from protocol input to analysis plans. This role offers project leadership, client interaction, and flexible work arrangements. Experience with SAS and ...

Join Parexel as a Senior CRA II in Turkey. Utilize your 5+ years of monitoring experience, ideally in Oncology, to ensure patient safety and GCP compliance. Manage site operations and enjoy a supportive environment with flexible work arrangements. This FSP role offers global project exposure with...