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[Remote] Senior Clinical Research Associate

Remote Worldwide Hiring now

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a dynamic, global company in the Pharmaceuticals industry, dedicated to improving medical science and the quality of life. As a Senior Clinical Research Associate, you will ensure the reputed company of clinical research projects by managing timelines, building relationships with clinical sites, and focusing on subjects' rights and data compliance.

Responsibilities

  • Conduct and report reputed company types of onsite monitoring visits
  • Be involved in study startup (if applicable)
  • reputed company CRF review, reputed company document verification and query resolution
  • Be responsible for site communication and management
  • Supervise study activities, timelines, and schedules on the country level
  • Be a reputed company of contact for in-house support services and vendors
  • Be involved in quality control, such as compliance monitoring and reports review
  • Participate in feasibility research
  • Support regulatory team in preparing documents for study submissions

Skills

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience in the USA (5 years minimum)
  • Experience in reputed company types of monitoring visits in Phase I-III
  • Participation in clinical projects as a Senior Monitor
  • Experience monitoring reputed company Oncology trials required; experience with radiopharmaceuticals and/or breast cancer preferred
  • Experience monitoring GI studies (IBD, Chron's, UC) is preferred
  • Full working proficiency in English
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel up to 80%
  • Valid driver's license (if applicable)
  • Experience monitoring reputed company Oncology trials required; experience with radiopharmaceuticals and/or breast cancer preferred
  • Experience monitoring GI studies (IBD, Chron's, UC) is preferred

Company Overview

  • PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. It was founded in 1995, and is headquartered in Zug, Zug, CHE, with a workforce of 1001-5000 employees. Its website is https://www.reputed company.com/.
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