Director, Intellectual Property

Job description

The Director, IP position will provide numerous development opportunities and report to and work directly with the Vice President, global Head of Intellectual Property. The primary responsibilities will involve the preparation and prosecution of complex patents while interacting with an impressive team of scientists, engineers, and executives, as well as outside counsel. You will be involved in all aspects of U.S. and ex-US patent prosecution related to Chemistry IP including small molecules, biologics, formulation, and process chemistry. Key Responsibilities Patent Drafting and Prosecution Using your scientific and technical expertise to: Serve as the primary point of contact for the various groups within R&D which are developing new products and discovering new technologies, Collaborate with scientific teams to identify patentable inventions and draft patents applications Liaising with/managing external counsel to draft patent applications, develop and implement global prosecution strategy for maximizing IP protection while avoiding infringement of valid third-party patents Performing extensive critical reviews of patents, patent applications, patent amendments, patent opinions and other patent-related documents for technical accuracy and full protection of company invention Portfolio management and overall IP strategy Supporting R&D colleagues by performing comprehensive searches of patent databases for invalidity, patentability, landscape, and freedom-to-operate analyses Developing and maintaining a deep understanding of the business, including: the research being conducted; products being developed, in/out - licensed, and commercial products in relation to the existing IP portfolio Assisting in providing guidance to R&D and commercial teams regarding patent and trade secret matters, and displaying ability to independently identify and develop IP strategies to benefit the business Traveling, up to 20% as needed, to Deciphera/ONO sites Other duties and responsibilities as assigned Advanced scientific degree: Ph.D. in the field of Organic Chemistry, Medicinal Chemistry, Biochemistry preferred, with 8+ years OR MS with additional relevant experience and 12+ years of hand-on experience will also be considered Registration with the United States Patent and Trademark Office (USPTO) Minimum of 8 years’ relevant professional experience in biopharmaceutical company, law firm, and/or life sciences industry Minimum of 5 years of hands-on experience at a law firm considered ideal, especially in: Drafting and prosecuting patent applications directly related to the life sciences industry IP strategy and/or development and management of patent portfolio Conducting prior art database searches for patentability and freedom-to-operate analysis Ability to work proactively, both independently and collaboratively, in a multi-disciplinary team environment, and to communicate clearly and effectively Self-directed: Ability to work independently and accommodate last-minute requests. Ability to prioritize multiple tasks and respond effectively to rapidly changing priorities and deadlines. Excellent organizational skills with the ability to handle multiple patent applications simultaneously in a fast-paced, deadline-driven environment while providing strong attention to detail Strong professionalism and commitment to ethical conduct; ability to handle confidential and proprietary information using excellent discretion and judgment Preferred Capabilities Excellent interpersonal skills to develop and maintain strong relationships across multiple functional teams; Strong service-oriented disposition. Ability to communicate across disciplines and functions. Skilled at managing outside counsel Proficient skills in MS Suite applications (Word, Excel, PowerPoint, Outlook), ChemDraw, SciFinder and other AI applications and IP software Positive Energy: Strong work ethic with a can-do attitude. Strong collaborator who brings energy, enthusiasm, and inspiration Patient Focus: Motivation to work with urgency and go the extra mile. The patient is waiting. Innovation: Open-mindedness and flexibility to embrace change Strategic Thinker: ability to grasp the overall landscape and design focused IP strategies to maximize protection and value of company’s assets Approach to Problem Solving: Analysis and evaluation of issues. Identifying pros and cons of issues. Proactively proposing strategies and solutions Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $218,000 - $300,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.​ Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera’s competitive total rewards strategy that also includes annual performance bonus, a long-term incentive plan, full range of benefits and other incentive compensation plans (if applicable) Benefits: Competitive salary and annual bonus. Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more. Generous parental leave and family planning benefits. Outstanding culture and opportunities for personal and professional growth. EQUAL EMPLOYMENT OPPORTUNITY INFORMATION Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis. Deciphera, a member of Ono Pharmaceutical Co., Ltd., is a biopharmaceutical company focused on discovering, developing, and commercializing important new medicines and providing hope to people living with cancer, neurologic and autoimmune disease. Deciphera is leveraging its proprietary switch-control kinase inhibitor platform and deep expertise in kinase biology to develop a broad portfolio of innovative medicines. In addition to advancing multiple product candidates from Deciphera’s platform in clinical studies, QINLOCK® (ripretinib) is Deciphera’s switch-control kinase inhibitor approved in many countries including the European Union and the United States for the treatment of adult patients with advanced gastrointestinal stromal tumor (GIST) who have received prior treatment with 3 or more kinase inhibitors, including imatinib. ROMVIMZA® (vimseltinib) is a kinase inhibitor approved in the United States for adult patients with symptomatic tenosynovial giant cell tumor (TGCT) for which surgical resection will potentially cause worsening functional limitation or severe morbidity, and in the European Union for adult patients with TGCT associated with clinically relevant physical function deterioration and in whom surgical options have been exhausted or would induce unacceptable morbidity or disability. The spirit of collaboration that has brought medications to life continues to guide how we operate, grow, and discover new breakthroughs. We cultivate an inclusive culture that values curiosity, creativity, and shared accountability—empowering individuals to challenge the unknown together. Deciphera offers competitive compensation, including equity-based compensation, and a comprehensive benefits package that includes medical, dental, vision, 401(k) retirement plan, life insurance and a flexible spending account for either health care and/or dependent care.