Staff

SibPharma represents numerous clinics and investigators in Siberia. Our centralized clinical trials process allows us to quickly match qualified investigators with appropriate studies. SibPharma provides sponsors with experienced investigators for Phase I-IV studies, as well as thought leaders and high target physician clinics for larger Phase III studies.

Besides its employed staff SibPharma is comprised of numerous associated high profile clinical research physicians and surgeons practicing in many high volume clinics. Our investigators are broad certified and regularly engage in clinical research studies.

SibPharma's Clinical Research Coordinators (CRC) are medical graduates with solid clinical research experience across all therapeutic categories. CRCs follow studies from regulatory preperation, and participate in developing study advertising too. SibPharma, cognizant of sponsors objectives, strongly supports our CRCs’ endeavors leading to accelerated study initiation, responsible screening and enrollment. CRC's play an active role to maintain ethical standards and ensuring all patients have equal opportunities to enroll in studies.

SibPharma places great importance on continuous quality assurance and internal auditing from the first study patient, onwards. Each member of our staff is participating in specialised training initiatives mainting and improving its professional abilities in the industry. English language skills are a key qualification and asset of our staff and SibPharma is actively increasing the number of fully bilingual employees.

Our medical staff is experienced in electronic data capture and fully supported by IT professionals.