Experience

iMEDGlobal Corporation

• United States
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Senior Executive

  • Feb 2020 - Present

  Support execution of end to end case processing activity including case triage, data entry, quality review, medical review and distribution. Support management of the assignment of cases to ensure on-time deliverables are met. Provide technical and administrative support to the team and act as a supportive point of contact for clients. Assist in ensuring project SLAs are met. Serve as backup for ensuring process, training and standard operating procedures are compliant as per client’s expectations. Assist in providing metrics to the client/internal stake holders as per agreed periodicity. Support in maintaining regular communications with client POCs to ensure smooth functioning of the project. Daily/weekly/monthly communication (if required) for query and issue resolution. Prepare documentation of minutes of all important meetings and circulate to all the participants in the form of minutes of the meeting. Support client/internal audits and inspections. Show less



IQVIA

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Drug Safety Associate

  • Jun 2015 - Jul 2019

  Initial receipt, Database searches as necessary, Registry and Triage of incoming cases to determine seriousness for prioritization of daily workflow. Completion of case processing (case data entry, labeling, approval numbers, manual Coding, narrative writing,) and quality review. • Clarification of unclear or illegible information from the Local Safety Officer or Call Centre and customer communication as per the project requirement. Discuss source documents, coding conventions and ad-hoc queries with Pharmacovigilance Physician. Show less

• Clinical process associate

  • Mar 2015 - Jun 2015



Manipal Hospital, Bangalore

• Clinical research Coordinator

  • Apr 2014 - Feb 2015

  Conducting the trial as per the Protocol Guidelines, recording all the data in the source document as per the visits, maintaining the records of the patient, entering data’s in the Case Report Form / Electronic Case Report Form, maintaining the Investigator site File, dispensing the Investigational Medicinal Product and Drug Accountability and reporting all the relevant events to the Ethics committee, Investigator, Sponsor / CRO, Medical Monitor, Institution, DCGI. Conducting the trial as per the Protocol Guidelines, recording all the data in the source document as per the visits, maintaining the records of the patient, entering data’s in the Case Report Form / Electronic Case Report Form, maintaining the Investigator site File, dispensing the Investigational Medicinal Product and Drug Accountability and reporting all the relevant events to the Ethics committee, Investigator, Sponsor / CRO, Medical Monitor, Institution, DCGI.