Employer: Daiichi Sankyo, Inc.
Category: Clinical Research
Job Type: Full Time
Location: Basking Ridge, New Jersey (NJ), United States
Job Code: J3T0G16RVTV9FZ4WZSD
Post Date: 06/06/2024
Daiichi Sankyo Group is a global pharmaceutical company with over 100 years of scientific expertise. The company focuses on innovative pharmaceutical therapies to improve standards of care and address unmet medical needs. With a presence in more than 20 countries and 16,000 employees worldwide, Daiichi Sankyo aims to become a "Global Pharma Innovator with Competitive Advantage in Oncology" by 2025. The company's research areas also include rare diseases and immune disorders.
The Study Associate Manager assists in planning and executing clinical studies under the supervision of the Study Manager within Clinical Operations. This role involves ensuring adherence to protocols, Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), FDA regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The key focus is on providing clinical trial management support and tracking CRO and vendor performance against project goals.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
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