This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Working within a highly qualified team our Clinical Research Associates (CRA's) identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV ensuring adherence to applicable regulations and principles of ICH-GCP.
Overview of the Role
- Working independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
- Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
Role Requirements
- With a University degree in medicine, science, or equivalent
- You should also have knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
- You will possess excellent written and verbal communication in English and local language
- Good interpersonal skills enabling you to deal with queries in a timely manner
- You must be available to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving licence