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Clinical Research Assistant

Clinical Research Assistant

Refined Reports Data

1 - 5 years

0 Lacs

pune maharashtra

Posted:1 month ago| Platform: Shine logo

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Skills Required

subject recruitment screening data management documentation communication regulatory compliance informed consent processes clinical trial data scheduling study visits ichgcp irb submissions

Work Mode

On-site

Job Type

Full Time

Job Description

Your role as a candidate will involve: - Assisting in subject recruitment, screening, and informed consent processes - Collecting, entering, and managing clinical trial data and documentation - Scheduling study visits, communicating with study participants - Ensuring regulatory and ethical compliance (e.g., ICH-GCP, IRB submissions) Qualifications required: - Proficiency in subject recruitment, data management, and regulatory compliance - Excellent communication skills and attention to detail This is a full-time position with benefits such as health insurance and Provident Fund. The work schedule is day shift, and the work location is in person.,

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Clinical Research Assistant