ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical de...
...Study Design: The Clinical Research Associate would be expected to:
Assist with the identification and selection of investigators to... ...and guidelines in the relevant regions.
Basic...
Clinical Research Associate II / Senior CRA - Cardiology
The Clinical Research Associate is the person in Trial Coordination and Site... ...strategic resourcing and FSP services to the biopharmaceu...
...Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regu...
...Clinical Research Associate
Responsibilities:
Pre-Trial:
Identify and qualify potential clinical trial sites and investigators.
Set up and equip trial sites with necessary materials and equipment.
Trai...
...custodian.
Compilation and Archival of clinical raw data.
Preparation of various solutions, Labels.
Measuring Height and Weight of Volunteer.
Registration of Volunteers.
Screening of Volunteers.
Pe...
Clinical Research Associate II / Senior CRA CardiologyThe Clinical Research Associate is the person in Trial Coordination and Site Management that serves as primary contact point between the sponsor and the investigational site. This position is assi...
...integrity of the subject data in the clinical trial database under Risk Based Monitoring (RBM) mode. The areas of activity include but... ...reviewing study data in the system for the signal ...
As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Clinical Research Associate
Shanghai office based
Wha...
Secunderabad
PHARMACEUTICAL RESEARCH ASSOCIATES SARL
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