© 2019 IPHARMA

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About us

IPHARMA is a well-established CRO that manages clinical trials in Russia and EAEU. Clinical branch of ChemRar group, and partner of Skolkovo Innovative center.

IPHARMA qualified staff (N=55)

 

Education

Experience

Role at IPHARMA

Natalia RABINOVICH,
General Director

Master in Finance from Stockholm University in 2005

Over 15 years of management in chemical and pharmaceutical industry

General management of IPHARMA since 2013

Oversees all financial operations and strategic partnerships

Clinical Department

IPHARMA clinical team consists of qualified staff with the medical, pharmaceutical and biological education. Medical and GCP knowledge let them provide high quality of data, qualified study documents and patients safety.

Careful management of a clinical study is of paramount importance; and IPHARMA’s well-trained Project Managers oversee all study aspects with careful attention to detail.

Project Manager coordinates all study activities and reports to the Sponsor (or its designee), oversees the study’s clinical team, and works closely with other departments. 

Education

Experience

Role at IPHARMA

Natalia VOSTOKOVA,
Chief Operating Officer

PharmD from Moscow Medical Academy n.a. I.M. Sechenov in 2004

PhD in 2017

Over 12 years in clinical research (clinical operations, commercial, and management)

Leads the company since 2012

Medical Department

Local fluency is critical when evaluating medical information and communicating with Principal Investigators in Russia. Most helpful is when it is combined with fluency in English, facilitating interactions with Sponsors.  

IPHARMA can provide medical expertise and safety oversight for clinical trials. Our Medical Advisors are fluent in Russian and English; and hold MDs and PhDs with substantial clinical experience in the following major therapeutic areas.

Education

Experience

Role at IPHARMA

Julia TRAKHTENBERG,
Medical Director

MD from Moscow Medical Academy n.a. I.M. Sechenov in 1997

Residency and postgraduate studies in Endocrinology and Diabetology in 1997-2006

PhD from Russian Medical Academy of Postgraduate Education in 2006

Over 15 years in clinical research (investigator research work, medical monitoring)

Head of the Medical department since 2012

Oversees all medical writing and safety monitoring activities

Data Management Department

Education

Experience

Role at IPHARMA

Pavel KHOLKIN,
DM Director

Graduated from the State University of Management in 1996 and the Project Management Institute in 2016

EDC development and management in Phase I-IV, BE and post-marketing trials

Head of IPHARMA DM Department since 2017

Regulatory Affairs Department

Education

Experience

Role at IPHARMA

Diana SAPOZHNIKOVA,

Director of Regulatory Affairs

Graduated from the Moscow Medical Academy in 2003; PhD in 2006

Over 15 years in clinical research (medical associate, medical director, regulatory affairs)

Registration of original, generic, and biosimilar drugs of Russian and foreign MAHs

Head of the Regulatory Affairs Department of IPHARMA since 2018

Quality Assurance Department

The foundation of IPHARMA’s Quality management system is strict compliance to ICH GCP requirements and local regulations.

Education

Experience

Role at IPHARMA

Oksana KARAVAEVA,
Director of Clinical Operations

MD from Smolensk Medical Academy in 1998

Residency in Endocrinologyin 1998-2001

Over 15 years in clinical research (clinical operations, data management)

Head of the Clinical department since 2012

Oversees all project management and monitoring activities

Business Development Department

Analysis of possibilities to promote the company and representation of IPHARMA in the Russian and foreign markets, new business development, the development and improvement of relationships with customers.

Education

Experience

Role at IPHARMA

Anna RASHINA,
BD Director

Belgorod State University in 2005

State University of Management in 2010

Over 12 years as PM at Central Lab (phase 1-4, BE, postmarketing trials), 50+ audits

Head of the BD department since 2014

Oversees all operations for IPHARMA business activities and managment key relationships clients

Administrative Department

The employees of the department control the document turnaround during clinical trials and control compliance with the local legislation. They control the regulatory and legal compliance during the process related to planning, conducting of clinical trials and information data processing.

Education

Experience

Role at IPHARMA

Vyacheslav ROGOV,

Administrative Director

Law school of Moscow Economic and Legal University in 2010

Over 10 years in clinical research (jurisprudence, audit, compliance)

Member of the Ethics Committee

Head of the Expert Group 2.2-2.4, Laboratory of program managemen and projects development in the field of Living Systems

Head of the Administrative department since 2013

Oversees all the regulatory and legal compliance during the processes related to planning, conducting of clinical trials and information data processing