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ICON plc
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Clinical Research Associate

Clinical Research Associate

ICON plc

2 - 7 years

10 - 11 Lacs

mumbai

Posted:Just now| Platform:

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Skills Required

assurance gcp research associate 2 clinical trials clinical development healthcare clinical research associate monitoring clinical research associate ii clinical data

Work Mode

Work from Office

Job Type

Full Time

Job Description

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

Collaborating with investigators and site staff to facilitate smooth study conduct.

Performing data review and resolution of queries to maintain high-quality clinical data.

Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your profile

Bachelors degree in a scientific or healthcare-related field.

Minimum of 2 years of experience as a Clinical Research Associate.

In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

Strong organizational and communication skills, with attention to detail.

Ability to work independently and collaboratively in a fast-paced environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver s license

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