 | | Friday, September 16, 2011 |  | | | |  |
UC Berkeley Extension Clinical and Regulatory Sciences
Get the specialized instruction you need to advance your career. UC Berkeley Extension offers targeted certificates and programs to provide the skills to design and manage clinical trials, navigate compliance issues, and ensure new products and processes adhere to U.S. and international regulatory specifications. Choose from programs in:
• Clinical Research Conduct and Management (available online)
• Quality and Compliance for Biotechnology
• Regulatory Affairs
Fall courses are open for enrollment. Learn more. | | | | | | |
Drug Discovery & Development
Drug Discovery & Development magazine delivers vital insight about the latest technologies and tools used to develop pharmaceutical products to key decision-makers
Request Now! | | | 
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 Advanced Concepts to Support Drug Development of Potent Compounds from R&D through Manufacturing (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.
COURSE SEATING IS LIMITED AND USUALLY SELLS OUT!
New Brunswick, New Jersey
Boot Camp I September 20 - 21, 2011
Boot Camp II September 22, 2011
Contact: Susan Custer at susan.custer@safebridge.com or 650-961-4820 X231 or www.safebridge.com. | | 
|  • Pharm Country (Edison, New Jersey)
Daiichi Sankyo
Sr Director, Clinical Development - Oncology
Oversees and manages a regional development program or multiple multinational phase II/III clinical trials in order to achieve a high quality product for the marketplace and business success for Daiichi Sankyo. Will finalize clinical development plans, protocol profiles and sections of key submission documents and be point of contact for interactions with regulatory-agency clinical reviewing divisions on clinical matters.
• Rocky Bio (Phoenix, Arizona)
Cubist Pharmaceuticals, Inc.
Clinical Business Manager - Phoenix West
Responsible for achieving and maximizing territory and account sales goals through account management, high level clinical proficiency and effective selling. The CBM will be the primary point of contact for Cubist with key hospital influencers and decision makers across key functional areas including but not limited to physicians, pharmacists and formulary committee members.
• Biotech Bay (South San Francisco, California)
Cytokinetics, Inc.
Manager, Clinical Data Management
Provides leadership and coordinates the activities of data management staff at the CROs. Review, and comment on CRFs, annotated CRFs, EDC supporting materials, and edit checks documents. Interacts with Statisticians, Clinical Trial Project Managers, and other personnel to provide support in the areas of data management, data validation, Data base lock, and metrics report generation.
• Genetown (Boston, Massachusetts)
PAREXEL International
Associate Director, Early Phase Clinical Data Services
General responsibilities include supervision and management of CDS Project Leads and staff, ensuring the group is trained, mentored and developed. Provide oversight of the execution and productivity of quality CDS Project Lead activities, ensuring adherence to regulatory and PAREXEL standards. Provide input to continuous productivity improvement. Ensure proactive planning takes place and provide issue resolution for the Group.
• BioMidwest (Chicago, Illinois)
Takeda Pharmaceuticals
Medical Director/Senior Medical Director, Clinical Science - Metabolic
Leads the development of the all components of the integrated development strategy and the resultant tactical clinical plan and study designs to support the global development of and establish the conditions essential for determining the safety, efficacy, medical usefulness, and marketability of multiple compounds.
• Get Noticed! Add your resume to the BioSpace Career Center!
• See more than 5,000 job postings in the BioSpace Career Center! | | 
Biotech Beach Career Fair
Job seekers can spend a day with HR representatives and Hiring Managers from top biotech, pharma, medical device and diagnostics companies in the Southern California region.
Candidates with a 4-year degree in the life sciences and a minimum of 2-years of industry related experience are invited to attend. (Equivalent work experience may be considered in lieu of a four-year college degree. PhD and Postdoc candidates welcome.)
Exhibiting companies are recruiting for positions in areas such as: QA/QC, clinical research, engineering, manufacturing, biostatistics, clinical data management, chemistry, regulatory affairs, and research.
Job seekers may register here.
• Biotech Beach Career Fair, San Diego, CA September 22, 2011
• BioMidwest Career Fair, Chicago, IL October 4, 2011
• Pharm Country Career Fair, Bridgewater, NJ October 5, 2011
• Biotech Bay Career Fair, Burlingame, CA October 11, 2011
• Bio NC Career Fair, Durham, NC October 20, 2011
• BioCapital Beach Career Fair, Bethesda, MD November 1, 2011
• Genetown Career Fair, Cambridge, MA November 7, 2011
More information about BioSpace's Career Fairs
BioSpace White Paper
Biotech Career Fairs For Job Seekers 101: Control Your Experience
By June Salvati, BioSpace Director of Events and Corporate Services | | | | | | 
Hot Company
Synteract, Inc. (San Diego)
Global Headquarters
5759 Fleet Street, Suite 100
Carlsbad, California 92008 U.S.A.
Phone: 760-268-8200 Fax: 760-929-1419
Established in 1995, Synteract is a full-service Contract Research Organization, dedicated to meeting the clinical development needs of the biotechnology, medical device, and pharmaceutical companies. We have earned a reputation for responsiveness and reliability - ask for references, our clients will attest to this! We have accomplished this by focusing on the unique needs of each client and tailoring our services to meet those needs, while maintaining the highest standards and meeting all requirements for superior quality.
More Company Profiles | | 
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Editorial & Production Staff: Lana Ho, Suvarna Sheth, Maysa Darwish, Tammy Liu
ClinicaSpace.com - Clinical Trials. Clinical Research. Community. | |  • ClinicaSpace is a registered trademark of BioSpace, Inc.
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