Assoc Director, Audit Monito - ReqCode 92383BR

Sandoz, a global leader in the rapidly growing generics industry, is a company in which doctors, pharmacists and patients worldwide have placed their trust for more than 100 years. With our 23,000-plus employees in more than 130 countries, we save and improve lives by developing, producing and distributing high-quality, affordable pharmaceuticals. Choosing Sandoz is always 'a healthy decision'. Through our work and our medicines, we have committed ourselves to improving the quality of life of people the world over. Our future holds many opportunities. Let's explore them together!

Job Description:The Corporate Compliance Department of Sandoz is searching for a full-time dedicated Compliance Auditor and Monitor.

Key deliverables will include (i) auditing/monitoring to help ensure compliance by the business with Sandoz' policy infrastructure, including field force monitoring, ad boards, speaker programs, promotional materials review procedures, T&E expenses, trade shows, national sales meetings, donations, as well as the monitoring/auditing of policies governing our medical, R&D, and regulatory departments, (ii) communicating deviations to the business, and providing it with tailored remedial training and/or suggested process/procedural changes to help prevent further deviations; (iii) following-up to ensure deviations have been remediated and are no longer occurring, and (iv) reporting overall findings and trends to the Compliance Officer and Corporate Compliance Committee.

Behaviorally, the ideal candidate will be detail-oriented, high-energy, and self-sufficient - driving projects to completion independently with the utmost integrity. Also essential are a can-do attitude and the ability to work collaboratively with internal business partners.
Minimum Requirements:Bachelor degree or Advanced degree preferred with 5 -10 years of experience as an auditor, preferably in the pharmaceutical or medical device arena, with a baseline understanding of US promotional laws and guidance such as the anti-kickback law, PhRMA Code, prohibition against off-label marketing, etc. Additional experience auditing/monitoring in the clinical research arena is a plus.