Amir Malka, Adv. - CEO
Mr. Malka founded Bioforum Applied Knowledge Center in 1998 and is serving as the group’s CEO for over a decade. The BioForum group is an international hub for the pharmaceutical, chemical, biotech and medical device industries, providing an extensive range of professional learning and educational programs, experts support and consultations. In 2007, Bioforum established it professional service arm- Bioforum Professional which consists of 3 independent companies providing an extensive range of professional applications in the clinical trials area.
Tali Azulay - VP Clinical Data Management
Ms. Azulay has over 10 years experience in clinical trials data management, during the years she has managed trials of different phases in Israel, Europe and USA. From planning the trial to database closure, Ms. Azulay was involved in the successful result of hundred of trials. She has a profound acquaintanceship with local and international regulatory requirements and the relevant standards. Ms. Azulay holds an M.A. in Experimental Psychology from Bar Ilan University, and B.A. in Psychology from Ludwig-Maximilians University, Munich, Germany. Additionally, Ms. Azulay served as an adjunct lecturer for Data Analysis methods at the Bar-Ilan University and is volunteering at the Juvenile Diabetes Research Foundation in Israel
Eyal Wultz - Clinical IT Manager
Mr. Wultz has been working in the IT industry for 18 years. In the past 10 years he has been working in the pharmaceutical industry specifically implementing solutions in the Clinical Development, Regulatory, QA, and LIMS areas, balancing between business requirements and regulatory requirements (21 CFR Part 11). Since 2006 Mr. Wultz has been working also with the CDISC Standards, converting legacy data and building automated solutions based on ODM, SDTM and ADaM. He has built one of the first CDISC-based clinical data warehouses in the industry, integrating patients, operational and safety data into a single central, unified repository, enabling clinical teams to perform cross-trial analysis. Mr. Wultz holds a B.SC in Computer Science.
Lusiane Lea Belaus - Medical Writer
Ms. Belaus has joined the clinical trials field following her MD studies in South America. Her experience includes pivotal international trials phase I, II and III. She is responsible for Medical Writing and Coding activities along with Clinical Quality Control Senior Associate role, ensuring protocol requirements accomplishment, clinical data integrity and consistency. Her daily work highlights strong interaction with study team in-house and in-site, as well as leading clinical data review planning and supervision from protocol review until study closure.
