Event details
Amgen, the Association for Women in Science and the Healthcare Businesswomen's Association are proud to present "From Molecule to Market: An Educational Panel Series About Careers in Drug Development." This three-part panel series will feature industry experts sharing career advice from various stages of the pharmaceutical development process, from early discovery and process development to clinical research, regulatory and marketing. The goal of each panel is to provide our audience with an understanding of the drug development process, the roles and responsibilities of the functions involved and offer advice from industry experts on what it takes to be successful in these roles. We hope this event will help early and mid-career women to expand their horizons, make informed career decisions and be inspired to achieve the next level professionally. The event will include a moderated panel discussion followed by an interactive Q & A with the audience.
The panel series kicks off on November 5 at Amgen with a focus on the early stages of drug development process: discovery, research, toxicology and early process development.
The panel will be moderated by Mary Ellen Cosenza, PhD (executive director of U.S. regulatory, Amgen, Inc.)
Featured panelists include:
• Cindy Afshari, PhD, DABT (Executive director, toxicology, Amgen, Inc.)
• Ingrid Joseph, DVM, PhD (Senior director of pharmacology and bioimaging, Agensys, Inc.)
• Jennifer Lafontaine (Director of cancer platform chemistry, Pfizer, Inc. La Jolla)
• Karen Miller, PhD (Director, early process development, Amgen, Inc.)
Students and non-members are welcome. Heavy appetizers and beverages will be provided. We look forward to seeing you at the event.
Learning objectives
1. Provide a better understanding of the early drug development process (discovery, research, toxicology and early process development)
2. Introduce industry experts and ' career development experiences and lessons learned
3. Better understand the roles and responsibilities of the functions involved during the drug development process
Agenda
6:00 PM - 7:00 PM Registration and networking reception
7:00 PM - 8:30 PM Moderated panel discussion and Q & A
8:30 PM - 9:00 PM Wrap-up/additional networking/adjourn
Event location
Amgen
One Amgen Center Drive
Thousand Oaks, CA 91320
805.447.1000
Directions
Sponsors
Speakers
Mary Ellen Cosenza, PhD (Moderator)
Executive director, US regulatory, Amgen, Inc.
Cindy Afshari, PhD, DABT
Executive director, toxicology, Amgen, Inc.
Ingrid Joseph, DVM., PhD
Senior director of pharmacology and bioimaging, Agensys, Inc.
Jennifer LaFontaine
Director of cancer platform chemistry, Pfizer, Inc. La Jolla
Karen Miller, PhD
Director, early process development, Amgen, Inc.
Registration information
Event is open to: HBA/AWIS members and nonmembers
Online Registration deadline: November 4, 2014
Onsite (walk-in) registration: Is allowed
Member rate:
$30 until October 28, 2014
$40 after October 28, 2014
Nonmember rate:
$50 until October 28, 2014
$60 after October 28, 2014
Student rate:
$30 until October 28, 2014
$45 after October 28, 2014
AWIN/AWIS rate:
$30 until October 28, 2014
$40 after October 28, 2014
Capacity
Is capacity limited? Yes
Space is limited to 300 registrants.
Cancellations/refunds
Is this event refundable? Yes
If yes, must be submitted in writing to events@hbanet.org by October 28, 2014; no refunds are available after this date.
Event questions/support
- Program contact for event details: Email marcia.g.beymer@gmail.com and/or call 602-819-7012
- Membership questions: membership@hbanet.org or 973-575-0606 ext 1
- Trouble with online registration: events@hbanet.org or 973-575-0606 ext 3
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