Parexel - Research and Development

Join Parexel Consulting as a Senior Regulatory Affairs Associate and serve as the Spain Local Regulatory Responsible (LRR) in Madrid. Leverage your 5+ years of Spanish RA experience to manage AEMPS submissions and lifecycle strategies. Enjoy flexible work, career growth, and a supportive global e...

Join Parexel as a Senior Regulatory Affairs Associate and serve as the Local Regulatory Responsible Person for France. Leverage your 5+ years of French RA experience to manage submissions (CP, MRP, DCP) and interface with ANSM. Enjoy a fully remote role in France with flexible work arrangements a...

Join Parexel as a Senior Clinical Research Associate (CRA) and play a key role in advancing global drug development. You will independently monitor oncology studies, ensuring patient safety and GCP compliance at sites across Poland. This role offers career growth, mentorship opportunities, and a ...

Join Parexel FSP as a Bioanalytical Sample Management Scientist in West Point, PA. This onsite role requires a Bachelor's degree with 1-5 years of experience in a biological science and strong GxP knowledge. You will manage GLP/clinical sample inventory, utilize LIMS, and coordinate shipments, en...

Join Parexel as a Senior Regulatory Affairs Associate. Leverage 5+ years of regulatory authority-facing experience to lead strategies and submissions for biopharma and device clients. Enjoy a supportive, global team with remote flexibility and significant career growth opportunities.

Join Parexel Consulting as a Regulatory Affairs Consultant. Leverage your 4-6+ years of CMC regulatory experience to develop strategies for FDA/EMA submissions. Enjoy a fully remote role in the US with flexible work arrangements and global client exposure. Drive product approvals in a supportive,...

Join Parexel as a Clinical Research Associate (CRA) in South Korea. You will ensure patient safety and protocol adherence while managing investigator sites on global projects. We seek degree-qualified candidates with site management experience and strong problem-solving skills. Enjoy flexible wor...

Join Parexel Consulting as a Regulatory Affairs Associate specializing in Advertising & Promotional Labeling. In this remote UK role, use your scientific degree and industry experience to review materials and ensure compliance with EU regulations. You will provide regulatory leadership, mitigate ...

Join Parexel as a Senior/Principal Medical Writer in this FSP role. Author key clinical documents like study reports for regulatory submissions. Enjoy a supportive culture, career development, and competitive benefits including private healthcare. Ideal for a life sciences graduate with excellent...

Join Parexel as a Clinical Study Team Assistant. You will manage the Trial Master File (TMF), ensuring compliance with ICH-GCP and SOPs. This remote/hybrid role requires 2-3 years of clinical administration experience and strong organizational skills. Enjoy a supportive, flexible environment with...