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Clinical Research Associate Job

A well trained professional made of sterner stuff can only execute clinical research associate job efficiently and competently.

Keeping in view the professional demands, a CRA must have a strong grounding in ethical considerations, international regulatory requirements, clinical trial conduct in agreement with global GCP and an appreciable understanding of allied activities like data management, quality assurance, regulatory documentation & submissions, pharmacovigilance and medical writing. ICH-GCP certification is inevitability and ought to be used to medical and pharmaceutical jargon.

Clinical research associate job is precisely linked to proper conduct of clinical study by coordinating with sponsors/contact research organization and site personnel. Quality assurance is the critical aspect and requires to be dealt with iron hand. The applicable regulatory compliant trial execution will be singly shouldered by a CRA. He will closely work with Principle Investigator and monitors scathingly the support staff whether the safety, wellbeing and respect of the trail subjects is met or not.

The industry requires clinical research associates and it is constantly in look out of fitting professionals who are highly informed and well qualified. A proper training will enhance the chances of cracking a clinical research associate job in a professionally managed company.

James Lind Institute is leading the way in providing self-paced online courses in clinical research arena primed by professional having years of experience in global clinical trial conduct.

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