At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary
Responsibilities
Qualifications
Education Qualifications
Bachelor's Degree in nursing or health care related field required
Experience Qualifications
Minimum of five (5) years of management experience in PV
Must have proven expertise in Drug Safety / Pharmacovigilance experience, including both investigational and marketed products
Extensive knowledge of AE and drug coding conventions (MedDRA, WHO-DD)
Extensive knowledge of FDA and familiarity with ROW regulations, clinical and safety databases
Must have Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GVP).
Travel Requirements
Ability to travel up to 10% of the time domestic and international.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment 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.
Salary Range:
USD$201,840.00 - USD$302,760.00