Regional Clinical Scientist - Home-Based (Us Or Canada)
By ICON At , Remote
High level of organizational and project management skills.
Experience in analysis and interpretation of clinical data (including safety and efficacy); working knowledge of GCP and clinical trial execution.
Life sciences degree (BS, MS, or Ph.D.) with clinical or pre-clinical research experience in the pharmaceutical industry or healthcare setting.
Experience working with clinical trial sites.
Experience in all stages of drug development.
Provides analytical support of clinical trial data, including assessment and follow-up of issues relating to protocol conduct and/or individual subject safety.
Media Search Analyst Us - Spanish Language
By TELUS At , Remote

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Sr. Production & Quality Manager (Us Or Hong Kong Based)
By Trafilea At , Remote
A minimum of 4 years of experience as a Production and Quality Manager or in similar roles is a must.
Solid experience in factory production and quality processes in the intimate apparel industry or at least the apparel industry.
Experience leading teams overseas is a must. If the teams are based in China is a plus.
Solid experience related to Quality procedures and Continuous improvement in a factory environment is a must.
A rich experience including the opportunity to collaborate with world-class talents. Encouraging transparency and open communication to all.
Production & Quality Sr. Manager
Clinical Research Associate Ll-Lll- Vaccines - Home-Based (Us) - Florida Region
By ICON At , Remote
Demonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, IVRS/IWRS and Electronic Data Capture platforms
Applies knowledge of ICON’s policies and procedures
Demonstrates excellent knowledge of ICH/GCP
Displays ability to manage investigative sites to facilitate trial deliverables
2 years of experience supporting clinical trials. No In-House or site level experience will be considered
Advanced skill in utilization of applicable clinical systems