Parexel

Seeking a Senior Integration Engineer in India with MuleSoft 4 certification and 7+ years' software engineering experience. You will design and develop high-quality APIs and integrations using MuleSoft Anypoint Platform. The role requires expertise in SOAP/REST, EIP patterns, and CI/CD within an ...

Join Parexel's Early Phase Clinical Unit in Glendale, CA, as a Research Associate - Certified Phlebotomy Technician. Utilize your active CA CPT license to conduct vital Phase I clinical trials, performing medical procedures and participant screenings. This role offers extensive training, career a...

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 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 as a Clinical Operations Assistant to advance global healthcare. Utilize your science degree and site experience to support clinical trials through document management and administrative tasks. Enjoy flexible hours, professional growth, and a collaborative environment on groundbreaki...

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...

Seeking an experienced Quality Manager to support global Biostatistics and Programming teams, with a focus on India. You will lead Quality Event support, audits, SOP updates, and consultancy, requiring 8-12 years in clinical research and expertise in ICH-GCP and CAPA. This role offers a key partn...

Join Parexel Consulting as a Senior Regulatory Affairs Consultant - Labelling. Utilize your EU labelling expertise to develop strategies for biopharmaceutical and medical device clients. This remote UK role requires strong project management and communication skills. Enjoy flexible work, career g...

Lead our Statistical Programming team in Hyderabad, Bengaluru, or Mumbai. You will manage project deliverables and a skilled team in diverse therapeutic areas, ensuring quality and efficiency in clinical data analysis. We offer flexible work, career growth, and a supportive, inclusive environment...