Description:
As a Clinical Research Executive at QPS Bioserve, your role will involve a variety of responsibilities to ensure smooth study conduct and compliance. Here are some of the tasks you’ll be involved in:
🔖Ensuring readiness of clinical units, emergency units, and equipment for study activities.
🔖Organizing regulatory documents, approved protocols, and informed consent forms in the Trial Master File.
🔖Arranging study-related documents as per protocol requirements.
🔖Coordinating subject enrollment during check-in and study completion.
🔖Performing study-related activities in line with GCP, principles, ethics, and regulatory requirements.
🔖Obtaining and documenting informed consent from subjects.
🔖Conducting subject training on study procedures.
🔖Coordinating with investigators for drug administration.
🔖Administering investigational drug products to subjects.
🔖Coordinating with clinical staff for various activities as per protocol.
🔖Reporting adverse events and coordinating with investigators.
🔖Ensuring subject compliance with study activities.
🔖Accurate transcription of data from source documents.
Job Details:
For clinical research Guidance and interview preparation enroll our online course.

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