Medical Assistant
- Assist the Principal Investigator and Sub-Investigators in clinical trials.
- Communicate with sponsors and Regulatory Authorities.
- Comply with GCP and site Standard Operating Procedure.
- Ensure protocol compliance.
- Obtain medical records and update patient charts.
- Performed ECG.
- Collect vital signs.
- Collect blood and urine specimen for analysis.
- Administer IP according to Pharmacy Manual.
- Package and ship laboratory specimen to central laboratory in accordance with IATA regulations.
- Maintain and update regulatory documents for review by CRA.
- Maintain laboratory supplies and equipment.
- Maintain study related materials.
- Administer subject rated scales.
- Register subject visits according to protocol using IVRS.
- Enter data in EDC according to Sponsor defined timeline
- GCP Certification
- IATA Certification