CTA - Clinical Trial Assistant - ר"ג
הגישו מועמדות בלינק https://svt.jobs/u/tKqX2
A biopharmaceutical company is looking for a
CTA - Clinical Trial Assistant
Role Responsibilities:
Support setup, maintenance, and close-out of clinical trial documentation (TMF/eTMF and internal system)
Track study progress including site status, enrolment, regulatory submissions, equipment, tasks and open items
Maintain and update study trackers, logs and documentation. in accordance with document control procedures
Coordinate meetings, prepare agendas and document meeting minutes
Liaise with investigative sites, vendors and internal clinical teams to support study activities
Support ethics and regulatory submissions, study materials preparation, audits and inspection readiness.
Assist with administrative activities and coordination of corporate events and conferences (local and international)
Full Time - On Site
Requirements:
At least 2 years of experience as a Study Coordinator or CTA in a large organization (pharmaceutical company, CRO or similar clinical research environment)
BSc degree in a scientific field
Valid GCP certification
English at a high level (spoken, reading and writing)
Experience with regulatory documentation
* משרה מס׳ #854767 מיועדת לגברים ונשים כאחד
A biopharmaceutical company is looking for a
CTA - Clinical Trial Assistant
Role Responsibilities:
Support setup, maintenance, and close-out of clinical trial documentation (TMF/eTMF and internal system)
Track study progress including site status, enrolment, regulatory submissions, equipment, tasks and open items
Maintain and update study trackers, logs and documentation. in accordance with document control procedures
Coordinate meetings, prepare agendas and document meeting minutes
Liaise with investigative sites, vendors and internal clinical teams to support study activities
Support ethics and regulatory submissions, study materials preparation, audits and inspection readiness.
Assist with administrative activities and coordination of corporate events and conferences (local and international)
Full Time - On Site
Requirements:
At least 2 years of experience as a Study Coordinator or CTA in a large organization (pharmaceutical company, CRO or similar clinical research environment)
BSc degree in a scientific field
Valid GCP certification
English at a high level (spoken, reading and writing)
Experience with regulatory documentation
* משרה מס׳ #854767 מיועדת לגברים ונשים כאחד