Site personnel (89 %) feel that sponsors of clinical trials should collaborate in the standardization
of electronic data collection practices and systems for investigative sites.
Perform medical data entry tasks under the supervision of the clinical manager Responsible for entering medical data entry into electronic health records and other
electronic data collection systems in an accurate manner
Duke Clinical Research Institute is an academic research organization that manages and conducts clinical trials for a number of biopharmaceutical sponsors and has used
numerous electronic data collection tools.
Laurence Colletti from the Legal Talk Network interviews e-discovery expert Bennett Borden about
how electronic data collection and analysis is increasing the efficiency and accuracy of large scale litigation.
In addition to roles in which he orchestrated large -
scale electronic data collections relating to litigation, audits, and regulatory requests, Peter has also testified as an expert witness in computer forensics on both state and federal courts.
kept assigned route courier vehicle clean, performed basic maintenance checks and reported any irregularities to the immediate supervisor, as well as keeping an accurate count for all items picked - up and delivered using manual (paper) or
electronic data collection devices.
Data from the CenterWatch study indicate that over 70 % of clinical trial sponsors and service providers feel that the adoption of
electronic data collection would be more rapid absent the fear of regulatory repercussions.
Perform data entry,
electronic data collection, and tracing to support clinical research and ensures efficient, timely delivery.