Team

Who works with us / What they do

Team Omnipharm s.r.o. is a flexible platform of experts with extensive experience in the implementation of projects in the health sector. Education and professional experience of our employees together with external collaborators enable us to form a well-qualified team for every project and meet its specific needs. We utilize a unique newly developed data entry system that allows flexible data assessment and possible future re-evaluation.

Jaroslav Černý Jaroslav Černý

Executive Director of Omnipharm Ltd.

10 years + 22 years of experience

Principal responsibility

  • Management of services in clinical trials
  • Medical writing
  • Pharmacovigilance
  • Regulatory services
  • Post-approval compliance Management of translation services

Detail

Work bio

After his studies at the University of Chemistry and Technology in Prague, Jaroslav completed his PhD studies at the Czech Academy of Sciences in Prague at the Institute of Organic Chemistry and Biochemistry. Later he also accomplished a Postdoctoral Fellowship / Ph.D. Program in Pharmacology at the Department of Pharmacology of School of Medicine at Yale University.

He has more than 10 years of experience in basic academic research and 22 years of experience in the pharmaceutical industry in positions of Medical Manager, Medical Director & Local Compliance Officer at Roche Czech Republic. As part of his responsibilities, he established successful clinical research teams (both within the Czech Republic and the CEE region), GCP and GVP quality control schemes, and teams responsible for drug regulatory agenda. He has collaborated with many renowned international and local service providers in clinical trials and was directly responsible for the quality of clinical projects in the Czech Republic. He has experience in managing projects, designing business activities, changing management, developing business teams and individuals, and defining key performance indicators.

He is the author and co-author of several original articles in the field of biochemistry and pharmacology.

Jiřina Nedvědová Jiřina Nedvědová

Executive Director of Omnipharm Ltd.

20 years of experience

Principal responsibility

  • Management of services in clinical trials

Detail

Work bio

Jiřina graduated from the Pharmaceutical Faculty at Charles University.

She has gained 20 years of experience in clinical research within several Czech affiliates of multinational pharmaceutical companies. She started her professional career as a clinical trial monitor, and then hold positions of senior clinical trial monitor, project manager, line manager and director of the Department of Clinical Development at Merck Sharp & Dohme CR.

She has great insight into the work of international and local CROs. The local Association of Innovative Pharmaceutical Industry endorsed her active and influential participation in the Working Group for Clinical Trials.

During her time at MSD, she established three well-operating and successful clinical trial teams and the whole department of clinical development.

František Mandys František Mandys

 

20 years + 22 years of experience

Responsibility

  • Management of services in clinical trials
  • Information Systems in clinical trials

Detail

Work bio

František graduated from the Faculty of Electrical Engineering of the Czech Technical University in Prague with a specialization in biocybernetics, in which he defended his dissertation work.

He worked for twenty years at several medical research facilities, lastly at the Institute for Mother and Child Care in Prague-Podolí. He focused mainly on the applications of informatics and statistics in clinical practice, epidemiology and management of healthcare systems.

Since 1995, he was engaged in management of Pharma clinical trials, from monitoring and project management to the position of regional director at Covance Ltd. Czech Republic.

Currently he serves as clinical trial consultant and develops innovative Information systems for clinical trials.

Zdeněk Tauber Zdeněk Tauber

 

6 years + 16 years of experience

Responsibility

  • Medical writing
  • Pharmacovigilance
  • Medical Consultant
  • Medical Monitoring
  • CT Feasibility

Detail

Work bio

Zdeněk graduated from the Medical Faculty of University Palackého in Olomouc.

After graduation he joined the Department of Histology and Embryology, at Palacký University, where he worked as a lecturer and researcher. In 1998, he completed his PhD studies in the field of immunohistochemistry. From 1996 to 2015, he worked at the Department of Haemato-Oncology at the University Hospital in Olomouc

He was also a member of the team for bone marrow transplantation. From 2000 to 2015, he worked at Roche Czech Republic in areas of hematology and oncology, first as a Key Account Manager and later as a Sales Manager and Team Manager of Oncology. He led successfully sales and marketing teams, participated in the commencement of local medico-marketing projects and brought new drugs to market.

Currently he participates in undergraduate teaching and scientific research and publishing activities at the Medical Faculty of UP in Olomouc.

Františe Nový František Nový

 

22 years + 16 years of experience

Responsibility

  • Medical Writing
  • Medical Consultant
  • Medical Monitoring
  • CT Feasibility
  • Translation services

Detail

Work bio

František graduated from the Faculty of Medicine at Charles University in Prague in 1977.

After graduation he joined the Radiotherapy Department at the České Budějovice Hospital. In 1978, he moved to the Clinic of Oncology at the General Teaching Hospital in Prague.

From 1999 to 2004 he worked at Aventis CR as a Clinical Research Associate with primary focus on projects in oncology. From 2005 to 2015, he worked as Medical Manager and then as Group Medical Manager primarily responsible for the oncology at Roche Czech Republic. Within his responsibilities he also conducted medical monitoring in phase II and III international clinical trials, prepared literature reviews and data intended for publications and presentations for collaborating physicians, and translated English medical texts (materials for clinical trials, SPCs, information for patients and other documents).

Jaroslav Hrubý Jaroslav Hrubý

 

37 years of experience

Responsibility

  • Statistics
  • Mathematical models
  • Security Data Analysis

Detail

Work bio

Jaroslav graduated from the Faculty of Mathematics and Physics at the Charles University in Prague and completed his PhD studies at the Czech Academy of Sciences in Prague.

He worked for 37 years at the Czech Academy of Sciences, with main focus on mathematics and physics. As a part of his successful scientific career, he also did research as a "visiting scientist" at universities in the USA, Australia and the former Soviet Union. For many years, he also worked as an external consultant for a number of major companies in the Czech Republic (including some pharmaceutical companies) with a major focus on mathematical modeling, statistics and analysis of security information and personal data.

He is a recognized expert in the field of cryptology, and is the Chairman of the Expert Cryptology Group which is a part of the Czech Math Unit.

Jiří Kopečný Jiří Kopečný

 

10 years of experience

Responsibility

  • Senior Clinical Research Associate

Detail

Work bio

Jiří graduated from the University of Chemistry and Technology in Prague, where he also completed his PhD studies in organic chemistry.

He worked as a Clinical Research Associate in several multinational and smaller CROs and as a freelance CRA. His experience spans across clinical international studies phases II, III and IV (including post-registration Pharmacovigilance studies) in study centers across the Czech Republic and the Slovak Republic. In particular, he has gained significant experience in clinical trials in cardiology, immunology, neurology, dermatovenereology, oncology and other therapeutic areas.

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