The OSI Oncology Sales Specialist has a vital role in selling Tarceva to customers by fulfilling our corporate vision of "Shaping Medicine, Changing Lives". Ensuring the appropriate use of our products through meticulous planning, problem solving, persistence in the face of adversity, and professionalism. Delivering the highest level of clinical and

Primarily responsible for lead data management activities within one or more project areas. Lead CDA for a project(s) with responsibility for all data management activities up to and including database lock. Involved with (e)CRF Design review. Responsible for: * database design for new protocols which includes validation (UAT) * ensuring timely and quality data are delivered to appropriate p

This position provides key financial support to Oncology R&D including acting as the prime financial liaison for: Research, Preclinical, CMC and Pharmaceutical Technical Operations (PTO), and the Tarceva collaboration with Genentech and Roche. Responsibilities include but are not limited to (i) Monthly and quarterly close (ii) preparing annual R&D budgets and monthly forecast updates worki

Primary responsibilities include managing all procurement activities. Provide leadership and direction to buyers which includes the purchasing and negotiating of materials, equipment, and supplies from key suppliers. Make final decisions on the issuance of formal company purchase orders. Evaluates buyers when reviewing vendor quotes and services to determine most desirable suppliers. Responsible f

Responsible for providing financial leadership for overall global Oncology R&D including financial oversight of three main areas: Research, Development and Pharmaceutical Technical Operations (PTO) which are comprised of over 30+ R&D departments. This position will provide business decision support and work closely with R&D management at all levels including VPs, department heads and p

Responsibilities primarily include (i) the monthly accounting close for clinical trials and other various accounts and (ii) working closely with the clinical operations and the research group on departmental and clinical trial budgets and preparing monthly forecast updates. Prepares journal entries, reconciles General Ledger accounts. Provides records of certain assets, liabilities and expenses. B

Our U.S.-based internships are paid and generally last between 9 and 12 weeks. Interns become part of a high-performance team. They work on challenging projects and actively participate in meetings. This brings interns exposure to key business areas. All internships include: Training through projects and tasks Educating about the pharmaceutical industry Mentoring by OSI employees

The position will be responsible for managing computerized systems validation and related quality control activities for the enterprise, reporting into the Enterprise Content Management division. Key Responsibilities will include: Oversee, define and drive validation direction of computerized systems for the company, and partner with process/equipment/methods validation for harmonization whe

Responsible for supporting all procurement activities to include the purchasing and negotiating of materials, equipment, and supplies from key vendors. Evaluate vendor quotes and services to determine most desirable suppliers. Responsible for managing the procurement process with an emphasis on providing excellent customer service to the scientific end user community. Bachelor's degree (preferred

Product Manager (PM) assists Marketing Director in key aspects of brand management and represents the marketing team at various internal and external meetings The PM is responsible for flawless execution of promotional tactics for the OSI Oncology's flagship product, Tarceva, working in close collaboration with the US joint venture partner. The PM provides strategic input into the development of U

OSI Pharmaceuticals Inc. currently has an opening for a Director/Sr. Director in our Drug Safety Department. The Sr. Director, Drug Safety will be responsible for all product safety activities for OSI's marketed and investigational agents for all therapeutic areas both domestically and internationally. The incumbent's primary role is to oversee all medical aspects of the drug safety activities

This position is responsible for directing biostatistical personnel and resources. The selected individual will participate in the design of clinical trials, create statistical analysis plans, assure that statistical analyses are performed in accordance with these plans, and co-author and review interim and final reports. Other responsibilities include assuring that timely and quality data are pro

This position is responsible for all clinical operations activities, which involves all operational activities associated with clinical study initiation, execution including site monitoring and management. The responsibilit8ies also cover clinical study and vendor contract and budget negotiations, clinical study records management, and clinical SOP's. The selected individual will be responsible

THIS POSITION WILL SPLIT ITS TIME BETWEEN ALL NEW YORK SITES UNTIL THE COMPANY RELOCATES TO ARDSLEY, NY. OSI Pharmaceuticals, Inc. is looking for a highly motivated / self-directed individual with outstanding verbal and written communication skills to administer the company's Computerized Maintenance Management System (CMMS). The position will be involved in the day to day

Reporting to the VP Global Regulatory Affairs in the US, this position provides CMC regulatory oversight & strategic technical regulatory input across all OSI project activities, to ensure that all CMC regulatory requirements/commitments are met with respect to development of new products and maintenance of existing approved products. Education/Experien

Our Clinical Research Department currently has an opening for an Associate Director/Director position. OSI will be consolidating its offices to Ardsley, NY in 2010. This position may initially be training and/or working at the Boulder, CO site, but will be required to move to NY when the timing is appropriate. The primary purpose of this job is to manage one or two Clinical Research Trials in

Our Clinical Research Department currently has an opening for an Associate Director/Director position. OSI will be consolidating its offices to Ardsley, NY in 2010. This position may initially be training and/or working at the Boulder, CO site, but will be required to move to NY when the timing is appropriate. The primary purpose of this job is to manage one or two Clinical Research Trials in

This position requires hands on knowledge of operating systems and server technologies; LAN networking and devices; must have a thorough knowledge of industry hardware types and interoperability; basic understanding of application software is necessary. Person in this senior role provides feedback, suggestions and guidance to system administrators located at other sites. Person in position must be

This position requires hands on knowledge of LAN networking and devices; operating systems and server technologies; must have a thorough knowledge of industry hardware types and interoperability; basic understanding of application software is necessary. Person in this senior role provides feedback, suggestions and guidance to system administrators located at other sites. Person in position must be