Senior Associate, Compliance Monitoring and Risk Assessment

Senior Associate, Compliance Monitoring and Risk Assessment Employer Daiichi Sankyo Location Basking Ridge - NJ Start date May 19, 2026 View more categories View less categories Discipline Clinical , Clinical Testing/Monitoring , Regulatory , Legal/Compliance Required Education Bachelors Degree Position Type Full time Hotbed Pharm Country , Best Places to Work Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job

Job Details Company Job Details Job Description Job Title:

Senior Associate, Compliance Monitoring and Risk Assessment Job Requisition ID:

1516

Posting Start Date:

5/19/26 At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary This role supports the execution of key compliance functions, including state drug price transparency reporting, compliance monitoring, and third-party due diligence activities. The position is responsible for ensuring the accurate and timely submission of regulatory filings while staying current with evolving state requirements. The individual will contribute to the execution of compliance monitoring plan, including field monitoring activities, and identification and remediation of potential risks. In addition, the role manages day-to-day third-party due diligence processes, including onboarding, risk evaluation, and coordination across cross-functional stakeholders. This position also provides project management support for strategic compliance initiatives, contributes to the development of policies and training materials, and prepares content for senior leadership communications and governance forums.

Responsibilities Third-Party Due Diligence :

Support the day-to-day execution of the DSI Third-Party Due Diligence program, ensuring adherence to established processes and governance standards. Facilitate the onboarding of new vendors, including completion and validation of due diligence requirements such as risk questionnaires, screening activities, and coordination with cross-functional stakeholders to obtain required approvals. Ensure ongoing evaluation and periodic review of existing third parties to maintain an accurate and current risk profile. Contribute to the development and implementation of communication initiatives to drive awareness and alignment across business units regarding due diligence requirements and expectations.

State Drug Price Transparency Reporting:

Manage day-to-day support of State Drug Price Transparency reporting requirements, ensuring the accurate and timely submission of all mandated filings, including price increase reports, new product reports, and quarterly and annual submissions. Maintain a strong understanding of evolving state reporting laws and regulatory expectations by proactively monitoring updates, participating in relevant compliance forums, and integrating changes into reporting processes.

Compliance Monitoring:

Support the development, execution, and reporting of the Compliance Monitoring Plan, including the use of monitoring tools, analytics, and field-based activities. Identify potential areas of non-compliance and contribute to the assessment, escalation, and remediation of identified risks. Maintain accurate, timely, and well-documented records of monitoring activities, findings, and outcomes in accordance with internal standards. Conduct field-based (in-person) monitoring and perform ad hoc reviews of records and supporting documentation as needed.

Project Management & Program Support:

Contribute to the execution of enterprise-wide initiatives and special projects, as assigned. Provide project management support for key compliance and operational initiatives, including tracking progress, coordinating stakeholders, and ensuring timely delivery of objectives. Assist in the development of materials and presentations for senior leadership and governance forums, including Compliance, Ethics, and Corporate Committees and the Board of Directors. Support the drafting and ongoing enhancement of policies and procedures related to compliance monitoring, representative licensing, third-party due diligence, and state price reporting. Contribute to the design and development of training materials and modules to support employee awareness and adherence to compliance requirements.

Qualifications Education Qualifications:

Bachelor's Degree, required preferably in quantitative discipline

Experience Qualifications:

3 or More Years Related work experience required 3 or More Years Demonstrated strong organizational/project management support required 2 or More Years Pharmaceutical industry and experience in monitoring group or pharmaceutical sales preferred

Competencies:

Demonstrated collaboration and partnership skills within and across teams Strong project management skills Attention to detail Process and systems-minded Strong learning agility Proficient in MS Office Suite of programs; specific experience using Excel (e.g., pivot tables, graphing, macros, etc.) System knowledge of tools used by the company (i.e., Email, Navex, VeevaPromomats, etc.

Travel Requirements:

Ability to travel up to 10% of the time. Field Monitoring requires travel within the U.S. Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. 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.

Salary Range:

USD$92,160.00 - USD$138,240.00 Download Our Benefits Summary PDF Entry Level Company Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 15,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for cardiovascular diseases, under the Group's 2025 Vision to become a "Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. For more information, please visit: www.daiichisankyo.com . Daiichi Sankyo, Inc., headquartered in Basking Ridge, New Jersey, is a member of the Daiichi Sankyo Group. To learn more about Daiichi Sankyo, Inc., please visit www.dsi.com .

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4568 Company info Website http://www.daiichisankyo.com/ Phone (908) 992-6400 Location 211 Mt. Airy Road Basking Ridge New Jersey 07920 United States Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert Similar jobs Regional Manager & Sr. Director, Latin America (LATAM) Rockville, MD Associate Director, PV Strategic Partner Management Basking Ridge - NJ Senior Medical Promotional Review Manager Plainsboro, NJ