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Associate Director, Global Knowledge & Information Services US/EU
Illinois-Chicago
6/14/2013 7:39 AM
OBJECTIVES: The Associate Director, Global Knowledge amp; Information Services oversees strategy execution, resourcing, and operational aspects of Takeda Global Knowledge amp; Information Services in assigned region(s). This position manages a team of regionally aligned Information Specialists and is accountable for meeting the information services needs of the global Ramp;D and commercial
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Manager, Regulatory Strategy
Illinois-Chicago
6/10/2013 10:21 AM
OBJECTIVES: * Plans/manage/executes all regulatory activities of all levels of complexity for project of responsibility in development and/or supports regulatory activities for assigned marketed product of responsibility. * Provides a regulatory strategic focus on non-clinical and clinical aspects of drug development and associated regulations. * Serves as regulatory lead on t
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Director / Associate Director of PV Sciences
Illinois-Chicago
6/5/2013 9:02 AM
OBJECTIVE: This position is responsible for oversight of activities, timelines, and cross functional coordination for documents coming from PV, including regulatory submissions and responses, aggregate reports, white papers, etc. The position is also responsible for Global oversight and supervision of PV specialists who support the above mentioned activities, including ensuring adequate re
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Manager, State and Federal Disclosure
Illinois-Chicago
6/5/2013 9:02 AM
OBJECTIVE: The purpose of this position is to manage Takeda's compliance with Federal and State transparency requirements as well as other ancillary areas such as restrictions on interactions with Health Care Practitioners (HCPs) or Health Care Entities (HCEs). This position will be responsible for understanding federal and state health care laws and regulations and ensuring that Takeda's
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Program Manager, Quality Systems
Illinois-Chicago
6/5/2013 9:02 AM
OBJECTIVES: The purpose of this position is to provide a regional resource to lead TGRD US functional teams in the identification and mitigation of systemic issues which may compromise the compliance of Takeda's drug development operations. The person in this position will work with PDD Global Quality Assurance and TGRD US project teams in the quality investigation, deviation and waiver pro
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Executive Medical Director / Therapeutic Area Advisor (CV / Metabolic)
Illinois-Chicago
6/5/2013 9:02 AM
OBJECTIVES: Responsible for ensuring ongoing review and agreement of the Therapy Area Strategy and associated documents formulated by the TA leader prior to their review and approval by appropriate governance committees. Oversees the development and execution of the Integrated Development Strategy (IDS) and overall Integrated Global Development Plan (IGDP). Responsible for review of syno
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Manager, Regulatory Strategy
Illinois-Chicago
6/5/2013 9:02 AM
OBJECTIVES: * Plans/manage/executes all regulatory activities of all levels of complexity for project of responsibility in development and/or supports regulatory activities for assigned marketed product of responsibility. * Provides a regulatory strategic focus on non-clinical and clinical aspects of drug development and associated regulations. * Serves as regulatory lead on t
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Senior Medical Director, Therapeutic Area Pharmacogenomics Liaison (Cardiovascular & Metabolic)
Illinois-Chicago
6/5/2013 9:02 AM
OBJECTIVES: Responsible for interfacing with various Therapeutic area units to design, develop and initiate pharmacogenomics (PGx) programs globally. Responsible for the review of synopses and Pharmacogenomics clinical trial design and results. Responsible for providing guidance to TA program leaders on the incorporation of Pharmacogenomics activities into various clinical programs. Prov
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Senior Director, Therapeutic Area Pharmacogenomics (Cardiovascular & Metabolic)
Illinois-Chicago
6/5/2013 9:02 AM
OBJECTIVES: Responsible for interfacing with various Therapeutic area units to design, develop and initiate pharmacogenomics (PGx) programs globally. Responsible for the review of synopses and Pharmacogenomics pre-clinical trial design and results. Responsible for providing guidance to TA program leaders on the incorporation of Pharmacogenomics activities into various clinical programs. P
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Principal Scientist / Fellow PK/ADME
Illinois-Chicago
6/5/2013 9:02 AM
Please note that the requirements specified in this posting are the basic qualifications required for the Principal Scientist PK / ADME; however, job title will be dependent on the candidate's level of experience in those requirements. OBJECTIVE: * In collaboration with PRD Drug Metabolism and Pharmacokinetic Research Laboratory (DMPK RL) colleagues, independently oversee and monito
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