• Find preferred job with Jobstinger
  • ID
    #6099468
  • Job type
    Full-time
  • Salary
    TBD
  • Source
    Ergomed
  • Date
    2020-11-25
  • Deadline
    2021-01-24
 
Full-time

Vacancy expired!

Job Description

Duties and Responsibilities:

  • To verify that the conduct of the study is in compliance with the currently approved protocol/amendment(s), with GCP, and with the applicable regulatory requirement(s), and report any deviation as per study procedure
  • To verify that the rights and well-being of human subjects, clinical study’s participants, are protected and conducts monitoring to confirm subject safety and data integrity
  • To identify the investigators and verify that the investigator has adequate qualifications and resources, as well as that, facilities, including laboratories, equipment and staff are adequate for safely and properly conducting the clinical study throughout the study period
  • To act as the main point of communication with Investigator and his team
  • When requested to support preparation of regulatory and / or EC submission
  • Participate in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Demonstratedon-site monitoring experience
  • 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
  • Valid driver’s license (if applicable)

Additional Information

We offer excellent chances to progress and develop. We work on a global basis on interesting projects within rare diseases, oncology, and neurology. This is an ideal position to develop a career in clinical drug development. It offers the chance to progress into clinical project management.

Vacancy expired!

Report job