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Senior Clinical Research Associate


Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow us to create more effective trials and determine outcomes faster.If that is your passion, we have a place for you.Senior / Clinical Research AssociateJob Responsibilities:Oversees the progress of a Clinical Trial, ensuring that it is conducted, recorded and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and the applicable Regulatory requirements.Administer protocol and related study training to assigned site.Establish regular lines of communication with sites to manage ongoing project expectations and issues.QualificationsRequirements -Degree in Science, with a major in Pharmacy, Biological / Life Sciences or Nursing from a recognized tertiary institutionMinimum 1 year of clinical monitoring experience in the pharmaceutical / CRO industry.For Senior Research Associate position, minimum 3 years clinical monitoring experience, preferably with some experience in leading clinical teams in the regionGood knowledge of drug development process, clinical trial monitoring procedures, medical terminology and GCP/ICH guidelines Excellent organizational and problem solving skillsStrong written and verbal communication skillsAbility to travel when required