Clinical Trials

Amir is a seasoned leader with over two decades of experience in life sciences and clinical trials. As the Chairman of IMP Clinical Supply Services Ltd., a company he established in 2009, he drives innovation in clinical trial logistics and supply chain management. Amir holds an LL.B. and is a member of the Israeli Bar Association. His extensive experience and knowledge of clinical trials have been the driving force behind IMP vision since company inception. Amir is a member of several life science and clinical trial associations and is an active advocate in helping to break down barriers to further advance the life sciences and healthcare industries in Israel.

Limor has over 25 years of experience in the pharmaceutical and cannabis industries. At the establishment of IMP, Limor joined the team and has been an integral part of the company structure. She has taken a lead part in building the company culture, quality management, and systems. As CEO, Limor is leading the strategic and operational growth of the company to become a significant service provider for clinical studies sponsors. Limor brings her experience in both manufacturing and development of commercial and Investigational Medicinal Products, quality management systems, cGMP, GDP and local regulations to develop IMP into a top-quality leader in the field. Certified by both the American and Israeli quality societies as a Certified Manager of Quality (CMQ), she has served as a Quality Director of IMP and as VP Quality of Bioforum group. Prior to that, Limor held positions as Quality Manager for LycoRed Bio and Nesher Solutions and as a member of the Quality Assurance team at RAFA. Limor holds an M.Sc. Pharm in Pharmaceutical Chemistry and a B.Sc. in Chemistry from The Hebrew University of Jerusalem, Israel.

Sofi Glam has over 10 years of experience in the pharmaceutical industry, with more than 8 years in clinical supply management. Throughout her career, Sofi has developed a diverse skill set in client management and a solution-oriented approach. Her strategic vision and commitment to excellence significantly contribute to our company’s success and growth.

As VP Business Development & Customer Success, Sofi leads strategic initiatives to drive business growth and enhance customer satisfaction. She is responsible for developing and executing business development strategies to expand market presence and drive revenue growth. Sofi collaborates with stakeholders to identify and capitalize on new business opportunities, implements customer feedback mechanisms to continually improve service delivery and product offerings, and oversees contract negotiations to ensure compliance with industry standards and regulations.

Anna has been in Pharmaceutical Services and Management for over 15 years. She has extensive knowledge and experience in Pharmaceutical regulation, Pharmaceutical Production, Patient-Centric drug preparations and Clinical Trials Management. As the former Deputy Director of Pharmaceutical Services at Tel Aviv Sourasky Medical Center (Ichilov), she led a team of professional Pharmacists and developed procedures to enhance Quality and Safety.

Anna holds a Master in Pharma and a Master of Business Administration (MBA). She is a Certified Quality Auditor (CQA) and a Certified Manager of Quality/Organization Excellence (CMQ/OE).

Roni has over 12 years of experience in the clinical research industry. Her  comprehensive background includes a robust foundation as a Clinical Research Associate (CRA) in CROs, sponsors representative  and also as a Lead Study Coordinator at Sheba Medical Center, providing a deep understanding of holistic aspects related to clinical trials from both the site and sponsor perspectives.

Roni is responsible for leading a dedicated team of professionals that ensures the timely and efficient delivery of clinical supplies, crucial to the success of our clients’ studies. She leverages her extensive experience to anticipate challenges, streamline processes, and maintain the highest standards of quality and compliance throughout the project lifecycle.

Roni’s expertise not only enhances the operational efficiency of our projects but also strengthens client relationships, as she is committed to delivering tailored solutions that meet the unique needs of each study. Under her leadership, our Project Management team consistently delivers excellence, driving the success of clinical trials and ultimately contributing to the advancement of medical research.

Bat-El has over 13 years of experience in the pharmaceutical industry of commercial Medicinal Products of Israeli’s companies and Global company with logistic centers. Bat-El filled different quality positions and has experience with quality and compliance according to cGMP, GDP, IMC-GMP, IMC-GDP, ISO and local regulations.

As part of the quality positions, she gained experience in defining and implementing processes and systems following the relevant regulations.

Bat-El’s position provides quality Supervisory oversight of all QMS areas to ensure that Clinical Supply and Medical Cannabis are processed and managed in accordance with current regulations as well as customer requirements, and to provide overseeing compliance within the organization with laws, regulatory requirements, policies, and procedures.

Bat-El holds a B.A in Health Systems Management from Ariel University and attended several professional courses including internal and external auditing, GCP courses, Risk-Assessment management, Quality Assurance of Computerized System, and Information Security auditing.

Lilach has 30 years of logistics experience including many years in the pharmaceutical industry working under a strict GDP environment. Lilach has successfully passed numerous audits in the storage and distribution area. She has served as Dispatch/Warehouse manager at World Courier. Lilach has High analytical abilities, planning and finding solutions in real time as well as managing priorities within time constraints.
Lilach is responsible for the on-going Clinical Supply Management (CSM) of the Warehouse according to GMP, GDP principles and IMP SOPs. She also manages the Medical Cannabis inventory according to Israeli Medical Cannabis (IMC) unit requirements.

Aviva has over 10 years experience in the biotech and pharma industries, with 3 years in the clinical supply management field. Before joining IMP, Aviva worked with companies to better understand, define, and emphasize their unmet medical need, work plans, and R&D milestones to develop grant portfolios to attain non-dilutive funding for project advancement. At IMP Aviva performs a crucial role in the growth and success of IMP by identifying new business opportunities while building and maintaining relationships with clients and partners. She is the first contact with new clients and enhances the set up phase by identifying client’s specific needs for their clinical trials, collaborates with vendors, and ensures the necessary regulatory documentation are reviewed and approved. Aviva holds a B.Sc. in Neuroscience from Bar Ilan University and an M.Sc. in Biomedical Sciences and Biochemistry from the Hebrew University.