Clinical Research Associate
Veeda Clinical Research
Total years of experience :6 years, 1 Months
Assesses potential site qualification: Reviews study requirements, conducts pre-study visits and drafts
pre-study evaluation reports.
● Participates in the implementation of clinical studies: Communication with investigators and their
staff; ensures compliance with terms and conditions; properly trains site personnel and writes initiation
visit reports
● Supervise the conduct of clinical studies: works as liaison between site personnel and the sponsor;
performs monitoring in the field; ensures compliance with protocols, regulatory requirements, and goodclinical practices; writes follow-up visit reports.
● Ensures the quality of the project: Verifies materials and data integrity; assists site personnel with
internal audits or regulatory inspections; and perform ongoing follow-up with the in-house project team.
● eCRF : Reviews and approve with verification of source data.
● Closes clinical studies: Verifies the integrity of investigator files; ensures availability of clinical and
non-clinical materials; jointly reviews with investigators the obligations inherent at the end of the study and writes closure visit reports.
● Team and Vendors Meetings: Attends Team Meetings, Contribute to create PMP, Meetings with
sponsors and other vendors