Clinical Research Monitor

Medtronic Ver Empresa

Não especificado

Medtronic, the world’s largest medical technology company with more than 85.000 employees, is looking for a Clinical Research Monitor. The Clinical Research Monitor is responsible for the oversight of clinical research conducted at investigational sites to ensure compliance with study protocols, applicable regulatory standards, IRB/EC policies and procedures and business policies.

Main responsibilities of the position will be:

  • Prepare and submit documentation for clinical studies implementation (regulatory authorities, etc.)
  • Assist in site study selection and initial and ongoing site personnel training
  • Act as a primary point of contact for study sites as requested
  • Perform site monitoring visits in accordance with study Monitoring Plan
  • Ensure compliance with the Investigational Plan, applicable regulatory, IRB/EC, and Medtronic standards, guidelines and policies
  • Prepare site visit reports and correspondence for all visits and report potential incidents
  • Quality control (protocol deviations, discrepancies in data, non-compliance to study protocols, etc.)
  • Identify site needs and provide solutions to facilitate the clinical trial process
  • Assist in the creation of corrective and preventive action plans and trending reports

The ideal candidate should have the following profile:

  • Required 2 year experience in CRO
  • Degree in Life Sciences, nursing or other health related disciplines
  • Fluency in English and Portuguese (Spanish highly valued)
  • Excellent communication and interpersonal skills
  • Strong organization, time management, problem solving and project management skills
  • High attention to detail and accuracy
  • Prone to frequent travels
  • Driver’s license

Medtronic will conduct the selection process internally in a confidential way.

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