Senior Data Engineer – Clinical Trials

We’re Hiring | Senior Data Engineer – Clinical Trials (Pharma) Remote | Nearshore | LATAMWe’re looking for a Senior Data Engineer with hands-on experience in clinical trials and pharmaceutical data environments to support ongoing and upcoming projects.This is a domain-specific role — strong cloud skills are required, but clinical trial experience...

Senior Clinical Data Science Programmer - Remote - BrazilICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Senior Clinical...

Job Opportunity Senior Clinical Data Science Programmer. We are driving innovation and excellence in clinical development. Develop and maintain programming solutions for CDMS (EDC systems), data validation outputs, and custom reports. Collaborate with data managers, project managers, and biostatisticians to integrate programming solutions into the overall...

Senior Clinical Data Science Programmer Role We are seeking a skilled Senior Clinical Data Science Programmer to join our diverse and dynamic team. This role is pivotal in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. As a Senior Clinical Data Science Programmer, you will contribute to the...

Job Overview We are seeking a highly skilled and detail-oriented Clinical Research Associate to join our team. The ideal candidate will have experience in conducting Phase 2 clinical trials, with a strong understanding of Good Clinical Practice (GCP), FDA regulations, and ICH guidelines. The CRA will be responsible for monitoring and managing clinical...

Contract CRA Project - 40 hours per week 1 year contract. Seizure or Epilepsy - CNS Job Summary:We are seeking a detail-oriented and experienced Clinical Research Associate (CRA) to monitor and manage Phase 2 Seizure study clinical trials. The CRA will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and...

Contract CRA Project - 40 hours per week 1 year contract. Seizure or Epilepsy - CNS Job Summary: We are seeking a detail-oriented and experienced Clinical Research Associate (CRA) to monitor and manage Phase 2 Seizure study clinical trials. The CRA will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and...

Project Manager Clinical Research Associate role available. The successful candidate will be responsible for ensuring a clinical trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol. This position involves collaborating with investigators, site personnel, and cross-functional teams to ensure the...

Hi Weare DATA Group and we are searching for the best talent Our goal is tosimplify our clients' lives with innovative IT solutions. We operate at globalscale and we are expanding to PortugalIf youare passionate and have the desire to make the difference, we want to get toknow you Join us to be part of this incredible adventureWhoare we looking for?...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...