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Objectives of this role Ensuring compliance with protocols, standard operating procedures, and Good Clinical Practice (GCP) guidelines. Conducting regular site visits to monitor trial activities and data collection. Reviewing and analysing clinical trial data for accuracy and completeness.

A research associate serves as the backbone of scientific exploration, conducting experiments, gathering data, and analyzing results to advance knowledge in their field. They collaborate with colleagues, design research protocols, and contribute to the development of new theories or technologies.

The research site is a controlled environment where clinical research, development and testing can take place safely with appropriate oversight. In these settings, patients take part in supervised clinical trials and other research activities.

The following skills are beneficial for clinical researchers to have: Data analysis. After tracking data, clinical researchers analyze it to make scientific conclusions. Observation. Public speaking. Writing. Organization. Attention to detail. Consider additional schooling. Apply for relevant positions.

CRAs are responsible for data collection and documentation as well as are often responsible for managing trial-related supplies and other research-related support tasks. The person in this role should be adept with electronic data capturing systems and analyses.

CRAs are responsible for data collection and documentation as well as are often responsible for managing trial-related supplies and other research-related support tasks. The person in this role should be adept with electronic data capturing systems and analyses.

Here are the top 6 factors to support a successful career as a CRA at IQVIA. Communication. As a CRA, you are the key liaison between management, the study site, and the sponsor. Relationship management. Attention to detail. Critical thinking. Time management. Stress management.

Some primary responsibilities for clinical research associates at clinical trial sites and sponsor locations include overseeing clinical trials on behalf of clinical research institutes, pharmaceutical companies or government agencies, developing, outlining and writing clinical trial protocols and ensuring compliance