Parexel careers
383 open roles at Parexel (Pharma & Biotech) in Remote, China Shanghai Shinmay, Taipei, paying $42.2k–$147.8k where the posting says so. Read from its own careers site. Search and filter these.
- Clinical Research Associate - All locations- FSP
- Senior Clinical Research Associate - Early Development - Central/NE Region - FSP
- Early Phase Clinical Pharmacology Solutions Consultant
- Senior Associate, Regulatory Submissions & Registration for MAA (Biologics)
- Clinical Trial Coordinator - FSP
- Executive Director, HEOR Modeling
- Manager, Central Monitoring - FSP
- Solutions Consultant - Logistics
- Proposals and Contracts Manager - Clinical Research
- Clinical Research Nurse (overnight)
- Senior Regulatory Affairs Consultant, CMC – Post-Approval Vaccines
- Regulatory Affairs Consultant, CMC – Biologics
- Regulatory Affairs Consultant (German and French language skills)
- Programming Lead (Samples, Kits, Data & Logistics) - FSP - Remote - Ireland
- Programming Lead (Samples, Kits Data & Logistics) - FSP - Remote (UK)
- Precision Medicine Operations Lead / SKDL Programming Lead - Spain - FSP
- SKDL Programming Lead - Poland - FSP
- Associate Software Quality & Test Analyst
- Senior Business Analyst
- Health Economics Consultant
- Health Economics Associate
- Senior Regulatory Affairs Consultant - Regulatory Project Manager
- Early Phase Clinical Pharmacology Solution Consultant
- Participant Recruitment Site Engagement Associate - FSP
- Clinical Trial Coordinator (Regulatory) - FSP
- Clinical Study Physician - Oncology - FSP
- Clinical Operations Manager-F- budgets and contracts - FSP
- Clinical Trial Coordinator - FSP
- Clinical Research Associate
- Manager, Production Services
- Clinical Trial Coordinator- FSP
- Senior Clinical Database Programmer - eCOA
- Clinical Laboratory Coordinator
- Regulatory Affairs Labeling
- Clinical Operations Assistant
- Senior Clinical Data Associate - South Africa (Remote) - FSP
- Clinical Data Associate II - South Africa (Remote) - FSP
- Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)
- Principal Clinical Database Programmer - eCOA
- Associate Clinical Operations Leader/Reviewer
- Associate Clinical Operations Leader/Reviewer
- Site Activation Partner - FSP (Study Start-Up Associate)
- Site Activation Leader
- Clinical Data Analyst I
- Associate/Site Activation Leader
- Manager, Data Management
- Depot Technician
- Clinical Research Associate II/Sr. Clinical Research Associate - All US Locations - FSP
- Sr. Clinical Research Associate - US - Midwest/Central Region - FSP
- Statistical Programmer II