CLINICAL RESEARCH COORDINATOR
SMO Connect Clinical Research Services
09/2023 - Present, Ernakulam,Kerala,India
- Screening subjects for eligibility using protocol specific inclusion-exclusion criteria and documenting them.
- Collecting data as required by protocol and timely completion of case report forms.
- Completes study documentation and maintains study files in accordance with sponsor requirements and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms, etc.
- Liaising with laboratories regarding research findings
Clinical Pharmacist Intern
CSI Holdsworth Memorial Mission Hospital
01/2022 - 12/2022, Mysore,Karnataka,India
- Auditing all the in-patient orders for drug name, strength, formulation, dosage and duration of therapy, therapeutic duplication and to check for possible drug interaction, if any as per hospital protocols.
- Monitoring of adverse drug reaction. Made recommendations in response to physician inquiries regarding medication dosage and usage to optimize patient care.
- Provided clinical pharmacy service such as medication reconciliation for taking patient's medication history with their current medication regimen to identify and resolve any discrepancies.
- Medication review and clinical audits on the floor.
indenting of drug and non-drug orders.
- Check the patient record at the ward discuss with Clinical
Pharmacologist.
