Clinical Research Associates - ALL LEVELS FSP /Single sponsor/Turkey

Parexel FSP is hiring Clinical Research Associates from all levels to join us permanently, full-time, and home-based.

Dedicated to a single sponsor in BioPharma, who is revolutionising healthcare by harnessing the power of science to benefit people, society, and the planet. Turkey is a vital part of their global network, hosting colleagues from every life sciences value chain segment. Their science-driven approach aims to transform healthcare and improve patient outcomes, while also fulfilling a purpose-led role in society.

Job Purpose

As a Clinical Research Associate (CRA)/Clinical Monitor, you will have local responsibility for the delivery of the studies at allocated sites and will be an active participant in the local study team(s). You will work in close collaboration with other Monitors and the Local Study Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner. You will be the main contact with the study site and will have responsibility for the proper conduct of the study.

The CRA is responsible for the preparation, initiation, monitoring, and closure of an agreed number of centres in clinical studies according to Procedural Documents, international guidelines such as ICH and GCP, as well as relevant local regulations, and ensuring that the centres deliver according to the commitment in the individual trials.

A CRA with longer tenure and experience may take on additional responsibilities, including tasks associated with the Local Study Manager.

Requirements

• Minimum 18 months of experience as a Clinical Research Associate conducting all visits.
• Experience gained ideally in Pharma, CRO, or Biotech.
• Good understanding of Clinical Study Management, including monitoring, study drug handling, and data management.
• Bachelor’s degree in a related discipline, preferably in life science, or equivalent qualification.
• Strong oncology experience.

Apply today!