JOB DETAILS

1.writing drug trial methodologies (procedures)

2.identifying and briefing appropriate trial investigators (clinicians)

3.setting up and disbanding trial study centres

4.designing trial materials and supplying study centres with sufficient quantities

5.providing clinicians with instructions on how to conduct the trials

6.collecting and authenticating data collection forms (commonly known as case report forms)

7.monitoring progress throughout the duration of the trial

8.writing reports

9.Commercial awareness

10.A logical and inquisitive mind

11.Positive organisational abilities

12.Excellent numerical, written and verbal communication skills

FUNCTIONAL AREA

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📌 Clinical Research Associate (Chennai)
🏢 SEVEN CONSULTANCY
📍 Chennai