Parexel - Research and Development, Remote work

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 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 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...

Launch your clinical research career with Parexel's APEX CRA program. This accelerated training role offers foundational experience in monitoring and site management on global projects. Enjoy a remote US position with comprehensive benefits, including ACRP membership and development programs. Ide...

Join Parexel as a Senior Clinical Research Associate (CRA) and play a vital role in accelerating treatments to patients. You will monitor global clinical trial sites, ensuring compliance with ICH-GCP and local regulations. This US-based role offers career growth, flexible work arrangements, and e...

Lead statistical strategy for clinical trials as a Senior Manager at Parexel. Utilize your PhD/MS in Statistics and SAS expertise to design studies and ensure regulatory compliance. Enjoy flexible work arrangements and career growth in the UK, contributing to impactful drug development.

Join Parexel's FSP team as a Clinical Research Associate. You will ensure patient safety and data integrity by monitoring global clinical trial sites. This role requires ICH-GCP expertise, strong site management skills, and the ability to travel. We offer flexible work arrangements, career develo...