Drug Safety Associate- I - Parexel International - Hyderabad, India
(2021-10)
- Maintaining a good working knowledge of the adverse event safety profile of the assigned drugs, labeling documents, client's guidelines, and SOPs, and Global drug safety regulations.
- Performs clear and accurate data capture of cases in accordance with client conventions/guidelines and Standard Operating Procedures (SOPs).
- Ensures that the expectedness, causality assessment and seriousness criteria are accurate for the events and MedDRA coding in accordance with "MedDRA Term selection: Points to Consider".
- Request follow-up and perform query management, as applicable.
- Prepares medically cohesive case narratives based upon the reported information.
- TRIAGE activity: From 1 year which included receipt of cases from different sources, acknowledgement of receipt, data verification, validity check, duplicate search and booking /registration of cases/
Subject Matter Expert, Medical Coding - VEE Technologies - Vasanth Nagar, Bangalore, India
(2019-12 - 2021-10)
- My roles and responsibilities included reviewing quality of care provided to patients.
- Educate providers on documentation guidelines.
- To determine if organizational policies are current and effective and optimize revenue cycle management.
- To summarize, the job was to review writing for insurance documents/ denial or approved record.
Drug Safety Associate Trainee - IQvia - Bangalore, India
(2018-05 - 2019-12)
- Worked for P2 team (Onco drugs) which included Zytiga, Darunavir etc.
- Assessing the safety of pharmaceuticals drugs once they're on the market.
- Using standardized guidelines, determine whether the medication causes any adverse reactions in patients and report their findings back to the pharmacovigilance department.
- Drug safety management in clinical trials and to process the necessary information and pass it onto other teams. Other medical cases including hospitalization, significant disability, congenital anomaly or other medically important events require this process to be completed in 2-7 days. Perform a check on overall medical cohesiveness and consistency of the document.
- Compares and analyses data provided by the affiliate with the data available on client application. Prepares ADR form/coversheet as required.
- Creates the case on the safety database. Performs clear and accurate data capture of cases in accordance with client conventions/guidelines and Standard Operating Procedures (SOPs).
- Ensures that the expectedness, causality assessment and seriousness criteria are accurate for the events. Ensures MedDRA coding in accordance with "MedDRA Term selection: Points to Consider".
- Request follow-up and perform query management, as applicable.
- Prepares medically cohesive case narratives based upon the reported information.
- Routes the case to the next workflow state as applicable in the safety database.
- Performs quality checks/validation checks. Clinical Research Co-Ordinator, Consortium Clinical research Center, Nagarbhavi, India January 2017 - October 2017 Worked on clinical trial oncology drugs on live patients.
- Coordinate with Principal investigator (PI) to help ensure that clinical research and related activities are conducted and performed in accordance with federal regulations and university.
- Assisted PI in study feasibility as requested.
- Conducted or participated in the patient consent authorization and completed study documentation, narrative notes if applicable and CRFs.
- Also, assisted PI in study closeout and storage of study documents.
Clinical Research Co-Ordinator - Consortium Clinical research Center - Nagarbhavi, India
(2017-01 - 2017-10)
Worked on clinical trial oncology drugs on live patients.
- Coordinate with Principal investigator (PI) to help ensure that clinical research and related activities are conducted and performed in accordance with federal regulations and university.
- Assisted PI in study feasibility as requested.
- Conducted or participated in the patient consent authorization and completed study documentation, narrative notes if applicable and CRFs.
- Also, assisted PI in study closeout and storage of study documents.
Dental Practitioner - Supriya Dental Clinic - T. Dasarahalli, Bangalore, India
(2008-01 - 2016-12)
- Dental practitioner in collaboration with Supriya Dental Clinic.
- Diagnosed and treated problems concerning patient's teeth and gums.
- Regular check-ups and cleanings in addition to more detailed procedures like root canals or installing brace was provided to patients.
- Patients and parents of patients were educated on maintaining proper oral health.
- Carefully documented all the medications, diagnoses, treatments and consultations and supervised the work of professional, technical and administrative staff.
