Parexel - IT - Software Development

Lead early-phase clinical trials as a **Project Manager** at Parexel, driving cross-functional teams to deliver life-changing treatments. This remote role requires 2+ years of PM experience (or 3-5 in related fields), ICH-GCP knowledge, and strong leadership. You will own sponsor relationships, m...

Join Parexel Consulting as a Health Economics Associate in India, focusing on modelling to evaluate cost-effectiveness for global reimbursement. Leverage your expertise in VBA, SAS, or R, along with a Master’s in health economics or a quantitative field. Enjoy remote flexibility, diverse client e...

Seeking a Scientist III for a long-term FSP role in Rahway, NJ, specializing in LC-MS and Analytical Support. This lab-based position requires a BS/MS in Chemistry with 3-5 years of experience operating Waters, Sciex, or Agilent LC-MS systems. Key duties include maintaining open access instrument...

Seeking a **Central Monitor II** in **Romania** to drive clinical trial oversight. You will implement centralized monitoring strategies, analyze data for trends, and identify risks using KRIs and QTLs. Requires a life science degree, 5+ years pharma experience, and strong clinical monitoring expe...

Senior Clinical Research Associate sought in Israel for a dedicated client role. Leverage 5+ years of oncology and site management expertise to oversee all monitoring visits. Join Parexel to mentor junior CRAs, work with world-class technology, and drive global drug development. Enjoy a premium s...

Join Parexel as a Clinical Research Associate (CRA) in Early Development Oncology, covering the Northeast US. Leverage your 3+ years of site monitoring experience and GCP/FDA expertise to oversee clinical trials from activation to database lock. Enjoy 60-80% travel, flexible work arrangements, an...

Seeking a Scientist III - Analytical Chemist (Drug Product) for a long-term FSP role in Rahway, NJ. This position requires hands-on expertise in UPLC, HPLC, GC, and Empower software for drug product analysis. Ideal candidates possess a BS/MS with relevant experience and strong skills in method de...

Seeking a Principal Medical Writer, Patient Safety for a remote role based in Bengaluru, India. You will independently lead complex aggregate safety reports, serving as a subject matter expert on regulatory submissions. Requires strong analytical skills, exceptional medical writing, and client-fo...

Senior Clinical Research Associate (Oncology) sought by Parexel in the UK. Leverage 5+ years of CRO/pharma experience and essential oncology/RECIST expertise to ensure patient safety and data integrity. This role involves global monitoring, regulatory compliance, and building strong site relation...

Senior Clinical Data Analyst sought by Parexel for remote roles in the UK, Poland, or South Africa. Leverage 5-8 years of pharmaceutical data management expertise and Phase I experience to lead global studies. Drive eCRF design, vendor oversight, and regulatory compliance (ICH/FDA, CDISC). Enjoy ...

Join Parexel as a Statistical Programmer II in Taipei, Taiwan. Leverage your SAS expertise and analytical skills to analyze clinical trial data, ensuring safety and efficacy. Collaborate on global projects, producing SDTM/ADaM datasets and regulatory submissions in a quality-focused environment. ...

Lead RWD Strategy as Director at Parexel in Spain, driving healthcare innovation through real-world data. Leverage 10+ years of CRO/Pharma experience and expertise in patient data models (OMOP, CDISC) to shape bid proposals and vendor management. This role offers the chance to integrate cutting-e...