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6,242 jobs found
30.08.2024
MSD
MSD Clinical Research Associate United States, Ohio, Lima
Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws...
Source Verification : conducts a comparison of data recorded on Case Report Forms against source documents, verifies Informed Consent Forms for accuracy and completeness, reviews regulatory documents and device accountability...
Source Verification: conducts a comparison of data recorded on Case Report Forms against source documents, verifies Informed Consent Forms for accuracy and completeness, reviews regulatory documents and device accountability records....
Source Verification: conducts a comparison of data recorded on Case Report Forms against source documents, verifies Informed Consent Forms for accuracy and completeness, reviews regulatory documents and device accountability records....
The CRA executes site initiation, monitoring, and close-out visits, and identifies potential risks, and implements corrective actions to address deviations and non-compliance. The CRA will be expected to travel up...
Responsible for evaluation, initiation, monitoring, close-out and other tasks associated with the management of clinical sites. Ensure the conduct of all clinical studies is in accordance with Good Clinical Practices,...
Responsible for evaluation, initiation, monitoring, close-out and other tasks associated with the management of clinical sites. Ensure the conduct of all clinical studies is in accordance with Good Clinical Practices,...
Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws...
A Clinical Research Associate (CRA) plays a key role in the tech industry’s clinical research process by managing the collection of data and information associated with clinical trial development and execution. This job involves working with internal teams as well as external vendors and research sites to ensure all data is collected, analyzed, and reported accurately and on time. The CRA is a hands-on position that requires problem solving, attention to detail, and an understanding of best practices in the clinical research process. As a CRA, you'll be asked to provide guidance and oversight for the design, development, and execution of clinical studies to ensure compliance with all regulations. This may include reviewing and approving trial materials, providing technical guidance to research sites, and overseeing the integrity of the trial data. You must also provide regular status reports and analysis of data to appropriate organizational staff. By working with Expoint, one will have the opportunity to work in a fast-paced and intense environment, continuously learning and staying on top of the latest advances in clinical research. In this role, you will be responsible for driving the success of a clinical study and helping to create a product that will have a meaningful impact on the lives of people.