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ICON plc
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CDC I Professional

CDC I Professional

ICON plc

3 - 6 years

4 - 7 Lacs

bengaluru thiruvananthapuram

Posted:1 week ago| Platform:

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Skills Required

assurance data management gcp pharma clinical trials clinical research healthcare life sciences oracle clinical data management

Work Mode

Work from Office

Job Type

Full Time

Job Description

Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures.

Review clinical and third-party data based on edit specifications and data review plans.

Issue clear, accurate, and concise queries to investigational sites.

As required, communicate effectively with peers, clinical data scientist and functional management.

Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation, dispatching of queries to investigator sites for resolution, etc.).

Your profile

Bachelors degree in a relevant field, such as Life Sciences or Healthcare.

Basic kNwledge of clinical data management within the pharmaceutical or biotechNlogy industry.

Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).

Strong attention to detail and the ability to work effectively in a fast-paced environment.

Excellent communication skills and the ability to collaborate with cross-functional teams.

KNwledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.

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