When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Parexel FSP is hiring Clinical Research Associates with 3 + years of experience to join us permanently, full-time, and home-based.
Dedicated to a single sponsor in BioPharma, who is revolutionizing 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 centers in clinical studies according to Procedural Documents, international guidelines such as ICH and GCP as well as relevant local regulations, and that the centers 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 3 years 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!
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BruntWork
BruntWork
