PHARMACEUTICAL 2013 - Optimal capacity planning and resource allocation for a portfolio of clinical trials

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Category PHARMACEUTICAL 2013

Deadline: June 20, 2013 | Date: June 20, 2013

Venue/Country: Online, U.S.A

Updated: 2013-05-03 18:05:17 (GMT+9)

Call For Papers - CFP

To become familiar with newest development in optimal capacity planning and resource allocation for a portfolio of clinical trials

Description of the topic

Efficient strategic capacity planning and resource allocation is becoming a hot topic for biopharmaceutical companies and Clinical Research Organizations (CRO) due to increasing pressure to reduce cost of drug development. It is critical for many clinical organizations to find a better approach to increase effectiveness in resource capacity planning, especially for portfolio of clinical trials.

When biopharmaceutical company plans to start new trials, optimal capacity planning solution means: (1) optimal resource utilization; (2) optimal resource allocation between ongoing and new trials; (3) optimal outsourcing strategy; (3) identification of resource bottleneck; (4) optimal scheduling of new trials; (5) optimal hiring and budget allocation strategy for a variety of employee roles, and (6) understaffing risk assessment.

Effective strategic capacity planning for CRO means optimal trials “throughput”, and their allocation across therapeutic areas, and stages of development.

Both types of organizations experience significant challenges related to resource reallocation due to trial cancellation or invocation of a new trial.

ORBee Consulting developed powerful decision making methodology based on rigorous mathematical models for optimal capacity planning and resource allocation in clinical research. Our technique saves money (up to 30%) by uncovering better resource allocation solutions.

Areas Covered In the Seminar

What you will learn:

How to apply optimization technology to capacity planning in biopharma

How to derive workload demand and supply (overview) on a role level

How to optimize capacity planning and resource allocation across portfolio of clinical trials for both biopharma companies and CROs.

How to identify resource bottleneck using optimization tools

How to reallocate resources due to inclusion or cancellation of clinical trials

How to calculate understaffing risk

Who will benefit

Biopharmaceutical companies, CROs, consulting companies

Portfolio managers

Business analysts

Business Development analysts

Project managers

Financial analysts

Resource planners

Executive management

About Speaker

Vladimir Shnaydman, Ph.D, ORBee Consulting, President (2004 ? current). The company’ focus is design and development of analytical tools and techniques for optimization of business solutions for life science industries. Company also provides consulting service, utilizing capabilities of developed tools and techniques.

Vladimir has BS & MS Electrical Engineering & Computer Science, MS in Applied Mathematics & Operations Research, and Ph.D. in Engineering. He contributed to many industries such as biotechnology, computer networking, data storages, water resources planning and management, telecommunications, transportation, and others. Dr. Shnaydman published more than 50 papers. He is co-author of three books.

Speaker : Dr Vladimir Shnaydman

Product ID : F62324

Schedule Date :

Thursday, June 20, 2013

duration : 12:30 to 01:30 PM EDT

https://compliance2go.com/index.php?option=com_training&speakerkey=62&productKey=250