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Tuesday, November 10, 2009 |
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Pharm-Olam has 25 offices among the most populated cities in Europe, Latin America, India, South Africa, and the USA to provide cost effective coverage for oncology studies of all sizes. Pharm-Olam has helped bring 2 oncology compounds to NDA approval and have conducted oncology studies in over 30 countries. The majority of our clinical staff are MDs or PhDs, including oncologists in strategic areas for clinical trials. The incidence of oncology indications and standards of treatment can vary widely, so let Pharm-Olam conduct a complimentary feasibility study specific to your protocol and study budgets to use in your resource planning.
Contact us at www.pharm-olam.com, info@pharm-olam.com, USA +1 (713) 559-7900, UK +44 (0) 1344 891121. |
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More Featured News |
SafeBridge Consultants, Inc. announces two Potent Compound Safety Training offerings (may be taken separately or consecutively)
The SafeBridge original Potent Compound Safety "Boot Camp"® (Boot Camp I) is a comprehensive two-day course in pharmaceutical potent compound safety focused on training EH&S and related professionals in critical technical concepts and proactive safety programs in pharmaceutical industrial hygiene, occupational and environmental toxicology, analytical chemistry, and risk communication.
The SafeBridge new Advanced Concepts in Potent Compounds from R&D through Manufacturing - Potent Compound Safety "Boot Camp"(Boot Camp II) is a one-day advanced course focused on case studies and problem-solving to address potent compound safety issues in discovery, development, contract manufacturing and commercialization. A suggested pre-requisite for the Advanced Concepts course is previous attendance at "Boot Camp I" and/or significant experience in environmental health and safety applications in the pharmaceutical industry.
COURSE SEATING IS LIMITED AND USUALLY SELLS OUT!
San Diego, California
Boot Camp I February 2-3, 2010
Boot Camp II February 4, 2010
Boot Camp I: First registration $1975 additional company representative $1775
Boot Camp II: First registration $975 additional company representative $875
Both Courses: First registration $2800 additional company representative $2600
Contact: Susan Custer at susan.custer@safebridge.com 650-961-4820 x 231 or www.safebridge.com |
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New Multi-Marketing Channel Strategies
• Provides an overview of the reasons behind the need for new marketing channels
• Explores the different channel mixes used to reach the pharma industry's diverse customer base, both patients and doctors
• Examines the use of online social media technology and uses in-depth case study analysis to examine the pros and cons of each marketing channel
• Evaluates the future of online technology and how it can be used by Pharma marketing teams
Click Here for More Information |
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• BioTechxus (Dallas, Texas)
St. Jude Medical
Director, Complaint Management Systems
This position is responsible for the management of the global complaint management process at St. Jude Medical Neuromodulation Division. Ensures global complaint management process is compliant with domestic and international regulations. Ensures timely and effective resolution and documentation.
• Biotech Beach (Santa Barbara, California)
Johnson & Johnson Pharmaceutical Research & Development, LLC
Associate Director, Regulatory Affairs
The primary responsibility of the Associate Director, Regulatory Affairs is to serve as Regulatory lead for the Mentor Biologics group through delivery of CMC expertise, regulatory strategy, and detailed project planning for US and global regulatory submissions.
• BioCanada East (Quebec, Canada)
Pharmaceutical Clinical Associates, LLC
Sr CRA Consultant (Oncology)
As a member of a therapeutically aligned Clinical Study Management team, the Sr Clinical Research Associate will be responsible for assisting in the planning, implementation, monitoring and management of clinical studies. Responsibilities also include maintaining the department's central files.
• Genetown (Home Base, Massachusetts)
PAREXEL International
Project Director
To deliver high quality, timely, and profitable projects. To provide overall project management of clinical trials or clinical programs.
• Pharm Country (New York, New York)
Autism Speaks
Psychometrician - Research
The selected individual must be experienced and able to perform duties that support the collection of phenotypic data for the Autism Genetic Resource Exchange (AGRE), a gene bank and data resource created in order to advance research in autism spectrum disorders.
• Biotech Bay (Sunnyvale, California)
Intuitive Surgical, Inc.
Medical Advisor
The Medical Advisor conducts early and pre-clinical scientific research and/or development. This position will investigate the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problems.
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MedImmune
One MedImmune Way
Gaithersburg, Maryland 20878 U.S.A.
Phone: 301-398-0000 Fax: 301-398-9000
View Jobs
MedImmune is the worldwide biologics business for the AstraZeneca Group. The company has approximately 3,000 employees worldwide and is headquartered in Gaithersburg, Maryland with facilities in Pennsylvania, California, Kentucky, the United Kingdom, and the Netherlands. UK facilities include vaccine manufacturing operations in Speke and antibody discovery and research laboratories in Cambridge.
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