Parexel - Research and Development, Remote work

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...

Join our clinical research team as a Clinical Scientist. You will support the scientific conduct of studies, including medical monitoring and protocol management. This role requires a Life Sciences degree or extensive clinical development experience, plus strong communication skills. It offers a ...

Join Parexel as a Clinical Research Associate in the US Midwest/West. Utilize your ICH-GCP knowledge and oncology experience to monitor sites and ensure patient safety. Enjoy a supportive team, career growth, and flexible work arrangements on global therapeutic projects.

Join Parexel as a Senior Clinical Research Associate (CRA) and play an integral role in accelerating treatments to patients. This remote US position involves national/international travel to monitor sites, ensuring compliance with ICH-GCP and local regulations. You will work on global projects ac...

Join Parexel as a Senior Clinical Research Associate (CRA) in a remote Canada role. Utilize your 3+ years of monitoring experience, preferably in Oncology, to ensure patient safety and trial integrity across global projects. This position offers extensive travel, career development, and work with...

Join Parexel, a leading global CRO, as a Biomarker Consent Specialist. You will author, review, and negotiate genetic and biomarker language in clinical trial informed consents. This remote US role requires 5+ years of global trial experience and expertise in genetic consents. We offer comprehens...

Lead statistical strategy for global 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 a flexible, supportive environment in Argentina with diverse project exposure and career growth opport...

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, ...