Parexel

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 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 Senior Regulatory Affairs Associate in Spain. Leverage your 5+ years of Portuguese Regulatory Affairs expertise to guide clients through EU and INFARMED submissions. Enjoy flexible work, career growth, and a supportive global environment while managing product lifecyc...

Join our team as a Site Contract Associate, working remotely from the UK. You will lead direct site-facing negotiations for clinical trial agreements and budgets. This role requires a related degree, clinical trial knowledge, and strong communication skills. Manage contracts from initiation to ex...

Lead GCP quality oversight for clinical trial programs as an Asset Quality Director. Utilize your 10+ years of experience in ICH GCP and risk management to ensure compliance and inspection readiness. This remote role in Argentina requires strategic use of quality data to guide cross-functional st...

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 our team in Harrow as a Pharmaceutical Services Specialist. You will manage Phase I clinical trials, ensuring compliance with GCP and GMP standards. Key duties include IMP assembly, dispensing, and full pharmacy study delivery. A relevant life science degree and experience in clinical trial ...