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GPAT India is seeking a Research Associate to perform quality control checks on study data, ensure compliance with GCP and SOPs, and monitor in-process activities such as dosing and sample collection. The candidate will verify pharmacy documents against source data and conduct facility system audits.
The position requires a Masters or Graduation in Pharmacy with 0-3 years of experience in clinical studies or QA.
Research Associate
To Perform Quality Control check of all study related source data (Registration Forms,Informed Consent Documents, Trial Master File, General Case Record Documents, Logbooks and Subject CRFs etc) compilation and submission of study related data to QA department within set timelines.
To ensure all the activities / processes are performed as per GCP, Protocol, SOP and applicable guidelines during study conduction.
To Perform monitoring of in process actitivties like Dosing, Sample collection, Sample Processing , sample segregation etc.
To Check Pharmacy related documents (IP receipt, shipping, logbooks, discrepancies etc.) against source data.
To perform system audit of clinical facility as per inhouse SOP.
0-3 years
Masters
Graduation in Pharmacy