Lowering Clinical Research Professionals Turnover Rate: A Condition for Successful Clinical Trials

March 13, 2013 - PRLog -- Description:

Employee turnover is one of the major problems that plague the clinical research industry. When employees leave, it makes a big impact on the organization, because they it is difficult to start getting immediate results from the new employee. This is in addition to the many difficulties involved in hiring the right fit, which is both time consuming and arduous.

The solution to this problem is to be a clinical research organization that has lesser employee turnover. How does an organization become one? The answers to questions to like this will be provided at this webinar.

The speaker, Calin Popa, brings his many years of versatile experience in the clinical trials industry to explain how organizations can overcome problems associated with employee turnover in this industry. As a result of the learning imparted at this session; participants will be able to considerably reduce their employee turnover.

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When:March 19, 10:00 AM PDT | 01:00 PM EDT

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By whom:

Calin Enea Popa, MD, CCRA is the Founder and President of Advanced Clinical Research Service Inc. a Canadian full-service CRO that provides CRO services and training to FDA and Health Canada regulated industries. He provides ICH-GCP training and training for FDA and Health Canada regulations.

He provides consulting services for the purpose of compliance review, drug accountability, site management, safety review, training site personnel, and to assure the integrity of clinical data. Popa has performed site audits and site audit preparation. He has conducted visits to train new CRAs (sign-off visits) and performs online training for CRAs and site staff regarding regulatory compliance and Electronic Data Capture.

He works closely with companies and sites to prepare them for audits. He holds the CCRA certification from and is an active member of the Association of Clinical Research Professionals. Senior Clinical Research Consultant, MD degree. CCRA (ACRP) with solid business, clinical research and medical care background.

Popa has broad international experience with a full range of clinical trials (phases I to IV, biotechnology products, diagnostics, medical devices, pharmaceuticals, vaccines) in a large variety of therapeutic areas. He also brings expertise in the areas of clinical monitoring, clinical science, medical writing, project management, proven working knowledge of ICH GCP and FDA/TPD/EMEA regulations, trainings and a host of specializations that range from cardiovascular to gastroenterology.

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For whom:

The webinar will benefit

o   CRO staff involved in the design of clinical trials

o   Industry Sponsors involved in development of drugs and biologics

o   Compliance Officers

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Duration: 60 minutes

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To enroll for this webinar, contact

webinars@globalcompliancepanel.com

Phone: 800-447-9407