At Biomapas, I handle full monitoring responsibilities and clinical trial site management, including start-up activities. My work builds on experience across clinical research organizations and therapeutic areas.
At Pharm-Olam, I managed clinical trial documentation and site activities from feasibility and selection through initiation and close-out. I also supported submissions to Regulatory Authorities and Ethics Committees, investigator payments and budgets, contract negotiations, and site management in the United States.
I’ve also worked as a pharmacist and pharmacy manager, including at Ltd. Veseliba Pluss, pharmacy “Kadagas aptieka.” I hold pharmacist and legal adviser qualifications, and my clinical research training includes Good Clinical Practice.
