Olga Yefimova – MD

Olga has extensive experience in the clinical study start-up environment. She has graduated from Medical University as an internal disease specialist and got therapy and nephrology specialist degrees at the Medical Academy of Post-Graduate Education. Olga started her career in Clinical Trials as Sub-Investigator in 2005 and continued her professional development in the study start-up after joining the CRO industry in 2007. Before joining Biomapas, she was working as a Senior Start-up Project Manager at Covance LLC and further back in her career as Senior Regulatory and Site Services Lead at Chiltern, Site Activation Lead at ICON, Senior Clinical Trial Specialist at Parexel.

Olga is experienced in the management of the study start-up phase of global clinical trials, starting from pre-award to SIVs; oversight of the submission activities in maintenance and at the stage of study closure. She supported and participated in RFPs and BDs, internal company initiatives and SOPs and start-up processes’ development.

 

Big Enough To Cover  All Your Needs. Small Enough To Care.

Discover the tailored solutions that Biomapas provides to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Regulatory Affairs

Pharmacovigilance

Medical Information