Regulatory Affairs Manager, Controlled Substances Monitoring Program

McKesson Corporation

Georgia

Remote

USD 85,000 - 142,000

Full time

2 days ago
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Job summary

McKesson Corporation seeks a Regulatory Affairs Manager to join the CSMP within our U.S. Pharmaceutical Distribution operations.

This individual contributor role conducts customer due diligence assessments, analyzes pharmacy data, and partners with Sales, Legal, Compliance, Operations and other stakeholders on controlled substance compliance matters. The position is remote with travel up to 5%, with in-office days at Las Colinas, Irving, TX preferred.

Qualifications

  • Degree or equivalent; typically 4+ years of relevant experience.
  • Experience analyzing data from multiple sources to support business, regulatory, or risk decisions.
  • Experience preparing written reports or assessments requiring analysis and attention to detail.

Responsibilities

  • Conduct comprehensive customer due diligence assessments for strategic account pharmacies per CSMP policies.
  • Prepare clear written reports documenting due diligence assessments, analyses, findings.
  • Analyze pharmacy ordering, dispensing, and other data to support regulatory compliance and due diligence.
  • Collaborate with Sales, Legal, Compliance, Operations and other stakeholders on strategic account matters.
  • Maintain knowledge of emerging trends related to pharmacy operations and healthcare data analytics.

Skills

Data analysis
Regulatory affairs
Written reports
Cross-functional collaboration
Regulatory compliance

Education

Degree or equivalent

Tools

Microsoft Excel
Tableau
Power BI

Job description

McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve - we care.

What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow's health today, we want to hear from you.

About the Role

McKesson is seeking a Regulatory Affairs Manager to join the Strategic Accounts team within our Regulatory Affairs Controlled Substances Monitoring Program (CSMP). This individual contributor role supports customer due diligence for strategic account customers within McKesson's U.S. Pharmaceutical Distribution business.

Reporting to a Director of Regulatory Affairs, you will conduct and document customer due diligence assessments, analyze pharmacy ordering and dispensing data, and partner with Sales, Legal, Compliance, Operations, and other stakeholders on controlled substance compliance matters.

This is an individual contributor role with no direct reports. The successful candidate will work independently while building effective partnerships across internal teams and with corporate compliance teams at national pharmacy organizations.

What You'll Do
  • Conduct comprehensive customer due diligence assessments for strategic account pharmacies in accordance with Controlled Substances Monitoring Program (CSMP) policies and procedures.
  • Prepare clear, concise written reports documenting due diligence assessments, analysis, findings, and supporting information.
  • Analyze pharmacy ordering, dispensing, and other relevant customer data to support regulatory compliance and due diligence activities.
  • Apply data analysis and sound judgment to evaluate information from multiple sources and support informed regulatory decisions.
  • Collaborate with Sales, Legal, Compliance, Operations, and other internal stakeholders on matters involving strategic account customers.
  • Serve as a Regulatory Affairs liaison with corporate compliance teams at national pharmacy organizations, building productive partnerships while maintaining regulatory and compliance standards.
  • Manage multiple assessments and competing priorities while meeting established deadlines.
  • Maintain knowledge of emerging trends related to pharmacy operations, controlled substance compliance, diversion control, pharmaceutical distribution, and healthcare data analytics.
Basic Requirements
  • Degree or equivalent and typically requires 4+ years of relevant experience.
  • Demonstrated experience analyzing data and information from multiple sources to support business, compliance, regulatory, or risk-based decisions.
  • Professional experience preparing written reports, assessments, or similar documentation requiring analysis and attention to detail.
Preferred Skills/Experience
  • Experience in regulatory affairs, regulatory compliance, controlled substance compliance, healthcare compliance, pharmaceutical distribution, pharmacy operations, or a related field.
  • Knowledge of controlled substance compliance, diversion control programs, or applicable healthcare regulatory requirements.
  • Experience conducting customer due diligence, compliance reviews, risk assessments, investigations, audits, or similar analytical reviews.
  • Understanding of retail, chain, or health system pharmacy operations.
  • Experience analyzing pharmacy ordering, dispensing, prescription, or other healthcare-related data.
  • Proficiency with analytical and reporting tools such as Microsoft Excel, Tableau, Power BI, or similar platforms.
  • Strong written and verbal communication skills, including the ability to communicate complex regulatory or analytical information clearly.
  • Ability to exercise sound judgment and navigate complex discussions with internal and external stakeholders.
  • Strong organizational skills with the ability to independently manage multiple priorities and deadlines.
  • Demonstrated ability to collaborate and influence across cross-functional teams and external partners.
Description of Travel or In-Office and Physical Requirements
  • Travel: Up to 5% annually.
  • Location: Remote role; Irving, Texas (Las Colinas) is highly preferred.
  • Ability to work independently in a remote environment and collaborate effectively with geographically distributed teams.

This position offers the possibility of a hybrid work arrangement based on recent updates to our in-office/workfromhome model. If located in DFW area, the selected candidate may be expected to work onsite at our Las Colinas office a minimum of two (2) days per week, with the remaining days worked remotely. Specific inoffice days may be designated according to team needs and business priorities.

McKesson complies with all applicable U.S. immigration laws and regulations. The Company does not provide employer support or sponsorship for any immigration related employment benefit for this role.

Applicants must be currently authorized to work in the United States on a fulltime basis without the need for employer support or sponsorship now or in the future. This includes having the legal right to work in the United States without the need for McKesson support or sponsorship for any immigration related employment authorization (e.g., H1B, O1, E3, H1B1, TN, F1 OPT, F1 STEM OPT, F1 CPT, etc.) now or in the future.

Our Base Pay Range for this position

$85,100 - $141,800

We are proud to offer a competitive compensation package at McKesson as part of our Total Rewards. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. The pay range shown below is aligned with McKesson's pay philosophy, and pay will always be compliant with any applicable regulations. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

McKesson is an Equal Opportunity Employer

McKesson provides equal employment opportunities to applicants and employees, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other legally protected category. For additional information on McKesson's full Equal Employment Opportunity policies, visit our Equal Employment Opportunity page.

McKesson is committed to being an Equal Employment Opportunity Employer and offers opportunities to all job seekers including job seekers with disabilities. If you need a reasonable accommodation to assist with your job search or application for employment, please contact us by sending an email to (United States) Disability_Accommodation@McKesson.com or (Canada) Accessibility@mckesson.ca. Resumes or CVs submitted to this email box will not be accepted.

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