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Senior Clinical Research Associate (US)  

KCR (company)

Posted on : 21 October 2017

Project Description

Location: Boston or East Coast of the US (office-based/home-based)

The duties associated with the role include:
  • Performing site visits and monitoring activities in accordance with protocol, GCP/ICH Guidelines and other applicable requirements
  • Ensuring overall integrity of study and adherence to guidelines, protocol and regulations
  • Taking an active role in the project team by providing feedback and suggestions for successful completion of the project
  • ​Leading, coaching and mentoring CRAs team to assist in their development and training
  • Responsible for execution of KPI`s for assigned staff and for all site deliverables within required time and budget
  • Providing leadership for the development and implementation of new training programs and improvement of current programs for assigned staff
  • University degree in life sciences/pharmacy/biotechnology
  • At least 3 year of independent monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) according to protocol monitoring guidelines, SOPs, GCP/ICH Guidelines
  • Proven experience with line management
  • Deep knowledge of monitoring procedures and entire clinical trial process
  • Computer competency
  • Fluent command of English
  • Ability to complete tasks in an accurate and timely manner
If you wish to apply, please submit your CV using the button below.*
*please note you need to have current right to work in US to apply