Description:

Summary:
This position is responsible for the protection of and maximization of A Pharmaceutical Company's US IP portfolio and foreign counterparts. This position will handle, among other things, all aspects of U.S. patent litigation, U.S. Patent Office proceedings, IP counseling, manage prosecution of a portfolio of patents and patent applications in the U.S. and globally, and provide legal support for licensing, co-promotion, co-development, clinical trial collaboration, co-marketing and acquisition agreements (among other types of agreements) in the pharmaceutical and companion diagnostic fields, including drafting, negotiating and reviewing such agreements for U.S., global and ex-U.S. territories.

Responsibilities:

Carries out pre-litigation investigations, assists in selection of outside litigation counsel, assists in the direction and management of assigned patent litigations and patent office proceedings (IPRs and PGRs) involving marketed and pipeline products; inputs to senior management (U.S. and Tokyo) on settlement options, and negotiates directly with third parties for strategic settlements of assigned IP related matters.
Provides IP legal support, as needed in negotiating, drafting and reviewing licensing, co-promotion, co-development, co-marketing, clinical trial collaboration, companion diagnostic, and acquisition agreements. Conducts patent due diligence for local licensing-in product candidates for A Pharmaceutical Company and global licensing-in product candidates.
Manages and advises on prosecution of a portfolio of patents and patent applications in the U.S. and globally (as assigned), including patent term extensions, and SPCs.
Works closely with development teams to monitor results, new uses, etc. arising during research and development of products and to manage disclosures and publications of such findings with Tokyo to ensure that all appropriate patentable matter is protected in a timely manner by the filing and prosecution of patent application(s) in the U.S. and worldwide (in coordination with A Pharmaceutical Company. Collaborates with Tokyo IP in obtaining and interpreting infringement/validity opinions authored by outside U.S. patent attorneys regarding early research and development compounds.
Works closely with teams for pipeline and marketed products, in order to manage/process patent term extensions, Orange Book listings, claims for regulatory exclusivity, as well as ensure that any new patent protections available are obtained for new uses, different results, etc.; counsels development teams for pipeline products on IP, regulatory, and contractual issues arising during the course of product development.
Monitors current developments in several key legal areas and provides the Tokyo IP and DSI's V.P., IP Business Development with updates regarding same. Recommends strategic policies and procedures in the U.S. and in Japan to maximize IP protection in view of new legal and regulatory developments.
Other responsibilities and tasks as assigned.

Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.

Education Qualifications (from an accredited college or university)

Bachelor's Degree In Chemistry or Biology sciences required
JD from Law School of recognized standing, and Bar Admission in NJ (direct admission or eligible for limited in-house licensing in NJ.) required

Experience Qualifications

7 or More Years post-law school experience in patent litigation and/or patent prosecution required
4 or More Years pharmaceutical industry experience preferred

Travel:
Ability to travel up to 10% Approximately 2 week-long trips to Japan each year.