Job Title: Manager of Regulatory Affairs -Work From Home (TX, OH, FL)
Posted by: McKesson Corporation on Oct 19, 2021
Location:
, TXJob Description:
McKesson requires new employees to be fully vaccinated for COVID-19 as defined by the CDC, subject to applicable, verified accommodation requests.
McKesson Corporation is a Fortune 8 company and is one of the largest providers of healthcare supply chain management solutions, retail pharmacy, medical & pharmaceutical supplies, healthcare technology, community oncology and specialty care in the United States with revenues of $231 billion in 2020. The company was founded in 1833 by John McKesson and Charles Olcott in New York with a focus on importing and wholesaling pharmaceutical products. United by our ICARE shared principles, McKesson's 80,000 employees work together every day to make better care possible around the globe – one product, one partner, one patient at a time.
Job Summary
This position will support the Regulatory Affairs Director of Threshold Management in connection with McKesson’s Controlled Substance Monitoring Program (CSMP). Position requires interaction with internal customers from the Regulatory Affairs team, as well as IT and other departments, on all matters relative to the program.
Key Responsibilities
Monitor customer purchasing trends of controlled substances
Assist the Director with project work related to controlled substances ordering limits, referred to as thresholds, and suspicious order monitoring requirements including reporting to federal and state agencies
Create dashboards and reports to assist the CSMP regulatory team with customer ordering and threshold related analyses
Serve as a point of contact for internal stakeholders to answer questions related to threshold management and suspicious order monitoring
Support IT and outside entities with data requests
Assist in the development, maintenance, and improvement of existing tools related to CSMP related data sets (e.g. threshold system information, suspicious order monitoring information, etc.) to assist the broader program team in their due diligence efforts
Assist in the development, maintenance, and improvement of existing tools related to CSMP related data sets to provide better program visibility for CSMP Senior Leadership
Assist with program documentation
Minimum Requirements
6+ years of relevant professional experience
0-2 years supervisory experience or equivalent experience
Critical Skills
3+ years of data manipulation experience
Advanced skills with SAP, Tableau dashboards and BW reporting
Strong communication and presentation skills to explain complex logic and metrics
Additional Knowledge & Skills
Advanced programming skills in SQL, VBA, and Python
Proficient in Microsoft Office (Word, Excel, Outlook, PowerPoint)
Advanced proficiency in Excel (preferred)
People management and relationship building skills
Possess working knowledge of Federal and State governmental regulations pertaining to the diversion of controlled substances
Regulatory experience related to controlled substances
Education
Four-year degree in related field or equivalent experience.
Must be authorized to work in the US. Sponsorship is not available for this position.
We take pride in our culture of connection and believe in a workplace where everyone can be their full, authentic self. We welcome and encourage veterans, individuals with disabilities and others with diverse perspectives to join our growing team. Your unique perspective and experience are valuable assets that can translate into a rewarding career path with us. Apply to join our team and help shape the future of healthcare!
McKesson is an Equal Opportunity/Affirmative Action employer.
McKesson Corporation is a Fortune 8 company and is one of the largest providers of healthcare supply chain management solutions, retail pharmacy, medical & pharmaceutical supplies, healthcare technology, community oncology and specialty care in the United States with revenues of $231 billion in 2020. The company was founded in 1833 by John McKesson and Charles Olcott in New York with a focus on importing and wholesaling pharmaceutical products. United by our ICARE shared principles, McKesson's 80,000 employees work together every day to make better care possible around the globe – one product, one partner, one patient at a time.
Job Summary
This position will support the Regulatory Affairs Director of Threshold Management in connection with McKesson’s Controlled Substance Monitoring Program (CSMP). Position requires interaction with internal customers from the Regulatory Affairs team, as well as IT and other departments, on all matters relative to the program.
Key Responsibilities
Monitor customer purchasing trends of controlled substances
Assist the Director with project work related to controlled substances ordering limits, referred to as thresholds, and suspicious order monitoring requirements including reporting to federal and state agencies
Create dashboards and reports to assist the CSMP regulatory team with customer ordering and threshold related analyses
Serve as a point of contact for internal stakeholders to answer questions related to threshold management and suspicious order monitoring
Support IT and outside entities with data requests
Assist in the development, maintenance, and improvement of existing tools related to CSMP related data sets (e.g. threshold system information, suspicious order monitoring information, etc.) to assist the broader program team in their due diligence efforts
Assist in the development, maintenance, and improvement of existing tools related to CSMP related data sets to provide better program visibility for CSMP Senior Leadership
Assist with program documentation
Minimum Requirements
6+ years of relevant professional experience
0-2 years supervisory experience or equivalent experience
Critical Skills
3+ years of data manipulation experience
Advanced skills with SAP, Tableau dashboards and BW reporting
Strong communication and presentation skills to explain complex logic and metrics
Additional Knowledge & Skills
Advanced programming skills in SQL, VBA, and Python
Proficient in Microsoft Office (Word, Excel, Outlook, PowerPoint)
Advanced proficiency in Excel (preferred)
People management and relationship building skills
Possess working knowledge of Federal and State governmental regulations pertaining to the diversion of controlled substances
Regulatory experience related to controlled substances
Education
Four-year degree in related field or equivalent experience.
Must be authorized to work in the US. Sponsorship is not available for this position.
We take pride in our culture of connection and believe in a workplace where everyone can be their full, authentic self. We welcome and encourage veterans, individuals with disabilities and others with diverse perspectives to join our growing team. Your unique perspective and experience are valuable assets that can translate into a rewarding career path with us. Apply to join our team and help shape the future of healthcare!
McKesson is an Equal Opportunity/Affirmative Action employer.
Education Level:
High school or ged
Pay Rate:
Commensurate with experience
Security Clearance:
None
Travel Requirements:
None
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About McKesson Corporation
McKesson Corporation is a Fortune 8 company and is one of the largest providers of healthcare supply chain management solutions, retail pharmacy, medical & pharmaceutical supplies, healthcare technology, community oncology and specialty care in the United States with revenues of $231 billion in 2020. The company was founded in 1833 by John McKesson and Charles Olcott in New York with a focus on importing and wholesaling pharmaceutical products. United by our ICARE shared principles, McKesson's 80,000 employees work together every day to make better care possible around the globe – one product, one partner, one patient at a time.
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