Intern, Clinical Safety and Pharmacovigilance-Quality Assurance in Bernards, NJ at DSI

Date Posted: 2/16/2018

Job Snapshot

Job Description

Join a Legacy of Innovation 110 Years and Counting!

Daiichi Sankyo, Inc. is the U.S. subsidiary of Daiichi Sankyo, Co., Ltd. The Company currently markets therapies in hypertension, dyslipidemia, diabetes, acute coronary syndrome, thrombotic disorders, stroke risk reduction, opioid-induced constipation, IV iron therapy and metastatic melanoma.

Job Summary

Assist CSPV-QA with development and enhancement of audit templates, creation of an audit universe master log, and development of automated audit risk assessment tools. Rotate through DSPD QA departments to support these activities. Participate in ad hoc projects as required.

Responsibilities

1. Develop new and enhance current PV-QA audit templates
2. Develop master log of PV-QA Audit Universe
3. Create automated risk assessment tools
4. Rotate to DSPD QA Clinical and GMP sections
5. Ad Hoc Projects

Qualifications

Education
  • Successful candidates will have a science background (pharmacy curriculum preferred) with a minimum of 3 years completion of College Science or Pharmacy.

Experience
  • Understanding of Pharmaceutical Industry and Adverse Event Reporting Requirements

Competencies
  • Good communication and time management. Ability to work independently and in team environment. Good attitude, willingness to learn and stretch, good planning, frequent communication with supervisor. Excellent computer skills. Proficiency in MS Word, Excel and PowerPoint.
Daiichi Sankyo, Inc., is an equal opportunity/affirmative action employer. All 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.