Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy. Headquartered in Denmark, Novo Nordisk employs approximately 33,300 employees in 75 countries, and markets its products in more than 190 countries Novo Nordisk’s B shares are listed on NASDAQ OMX Copenhagen (Novo-B).
Post : Business Process Supervisor
Job Description
• Support in facilitating the US healthcare compliance program, raising awareness of the program and fostering accountability for compliance throughout the organization
• Reviews department wide policy and procedures and obtains necessary feedback from SMEs to provide relevant updates to policy owners as they relate to the Compliance Department
• Responsible for Third Party Representative process for the department (e.g. LDDR responsibilities)
• Maintains understanding of Laws and regulations, enforcement actions and evolving practices relevant to Pharmaceutical ethics & compliance and proposes updates to Ethics & Compliance program, as appropriate
• Manages the review and timely reporting of all government requirements while understanding local and global impact
• Recommends enhancements to systems, processes and technologies for government reporting
• Maintains understanding of applicable laws and regulations, enforcement actions and evolving practices/trends relevant to pharmaceutical compliance
Candidate Profile
• A Bachelor’s degree from an accredited institution required
• A minimum 10 years combined pharmaceutical, legal, regulatory and compliance experience required OR a minimum of 8 years’ experience if accompanied by an Advanced degree or certificate (MBA, JD, PMP etc…)
• Working experience with Big 4’s within compliance division is required
• Functional knowledge and understanding of Anti-Kickback Statute, the False Claims Act, FDA rules and regulations regarding the promotion
• Excellent communication and organization skills, strong report writing skills is required
• Ability to manage multiple projects concurrently and collaborate across several functional areas
• The ability to think objectively and use sound reasoning principles
• Proactively drives the local compliance program
• Builds and maintains strategic relations with internal and external stakeholders
• Supervisory experience preferred
Additional Information
Experience : 10 years
Qualification : Bachelor’s degree
Location : Bangalore
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Compliance & Ethics
End Date : 10th May, 2018
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