IRFANULLA shaik

Clinical Research Associate
March 2012- February 2013
Merck Serono, India

Clinical Research Coordinator January 2011- Feb 2012
Bollineni Super Speciality Hospital, India


Responsibilities:
• Learn protocol and co-ordinate how study will be conducted at the site.
• Study initiation, conduct and completion.
• Develop study source documents, visit schedules, Pre-screening questionnaires letters and regulatory files.
• Ensure proper study product storage and accountability.
• Close study with sponsor and IRB and store the record appropriately.
• Ensure study was conducted according to the GCP Guidelines & other regulatory requirements.

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