Associate Manager, Market Access Analytics

The Market Access Analytics Associate Manager selects the appropriate data sources to develop reports and dashboards of Real-World Evidence for market access.
Working in collaboration with statisticians, data managers, clinical team, CMOs, data vendors, IT, Reimbursement & Health Economics and quality assurance staff, the Market Access Analytics Associate Manager will provide market access data analysis reports and tools that enhance business processes.
What You’ll Work On • Collaborate with market access team to clarify and finalize user requirement specifications for market access data analysis tools and reports.
Communicate with selected vendors and/or build reports and/or tools to meet market access user requirements.
• Lead technical projects like the development of risk-based monitoring programs, complex reporting and cross-form query building outside EDC, integrations between EDC and other systems, and data warehouse projects.
• Contribute to the development and maintenance of the data warehouse used to manage libraries of real-world evidence study data including image, source document and data files.
• Develop dashboards and reports to support the market access team by choosing the right technique and software for each problem.
• Independently develop reports to execute study-specific data review/cleaning plans • Perform complex programming such as data import/export and data transposition (Extract-Transform-Load (ETL)) accurately.
Use advanced procedures and options.
• Assist in the setup of programming timelines and deliverables for projects as required.
• Assist in addressing external application vendor issues, integrations, and implementations.
• Provide support for implementation of upgrades and new modules of remotely hosted vendors, acquiring all necessary documentation.
• Partner with organizational stakeholders to create and implement data analytics best practices.
• Contribute to the build and test of Real-World Evidence databases by defining study requirements specifications such as data validation specifications and participating in User Acceptance Testing (UAT) as needed.
• Participate in and contribute to project discussions.
Communicate with team members on a regular basis.
• Utilize reports and data collection technology to identify possible data errors and questionable data trends.
• Participate in audits as required.
• Provide support to senior level market access data analysts as needed.
• Proactively provide process improvement feedback to management and provide input in SOP and standards updates/development.
• Maintain and continue to gain a broad overall knowledge in the field of real-world evidence data management.
• Attend training classes and professional meetings as required.
• Create training materials for market access users and developers.
• Document data sources and data mapping.
• Create analytical data models and tools to help empower market access teams.
• Follow data standards policies, procedures, practices, and regulations for Real-World Evidence data analysis reports and tools throughout the process of collection and submission of RWE data.
• Provide technical support and training on reports and tools for market access staff • Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures.
• Understand relevant security, privacy and compliance principles and adhere to the regulations, standards, and procedures that are applicable to the Company.
• Ensure other members of the department follow the QMS, regulations, standards, and procedures.
• Perform other work-related duties as assigned What You Contribute • Bachelor’s degree in Mathematics, Computer Science, Economics, Life Science, or related field with 4+ years of experience.
• Master’s degree preferred.
• Relational database experience preferred.
• Knowledge in data visualization, dashboarding or analytical report programing experience.
• Solid hands-on knowledge of at least one programming language (e.
g.
, Python, SAS, R MATLAB, Sharp, Visual Basic, SQL required.
• Experience in the analysis of medical scientific data preferred.
• An understanding of the software development lifecycle process is preferred.
• Experience with real world evidence databases (e.
g.
, Medrio, InForm, RedCap, OpenClinica, RAVE) a plus.
• Knowledge of core Real-World Evidence data management applications (Clinical data management systems, electronic data capture, query tools, web browser, MS Office suite) a plus.
• Able to take initiative on own project responsibilities.
• Excellent attention to detail and ability to multi-task taking into account established project priorities are essential.
• Demonstrated expertise in use of required technology.
• Medical device, pharmaceutical, biotech, or other regulated industry experience desired.
• Strong oral, written, and interpersonal communication skills.
• Proficiency with MS Word, Excel, and PowerPoint.
• Excellent organizational skills with ability to prioritize assignments while handling various projects simultaneously Working Conditions General office environment.
Willingness and ability to work on site.
Potential exposure to blood-borne pathogens.
Requires some lifting and moving of up to 15 pounds.
Must be able to move between buildings and floors.
Must be able to remain stationary and use a computer or other standard office equipment, such as a printer or copy machine, for an extensive period of time each day.
Must be able to read, prepare emails, and produce documents and spreadsheets.
Must be able to move within the office and access file cabinets or supplies, as needed.
Must be able to communicate and exchange accurate information with employees at all levels on a daily basis.
Annual Base Salary Range: $107,064 - $167,911 / year We offer a competitive compensation package plus a benefits and equity program, when applicable.
Individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location.
What We Offer •A collaborative teamwork environment where learning is constant, and performance is rewarded.
•The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases.
•A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, an employee stock purchase plan, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).
Penumbra, Inc.
, headquartered in Alameda, California, is a global healthcare company focused on innovative therapies.
Penumbra designs, develops, manufactures, and markets novel products and has a broad portfolio that addresses challenging medical conditions in markets with significant unmet need.
Penumbra sells its products to hospitals and healthcare providers primarily through its direct sales organization in the United States, most of Europe, Canada, and Australia, and through distributors in select international markets.
The Penumbra logo is a trademark of Penumbra, Inc.
Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, age, disability, military or veteran status, or any other characteristic protected by federal, state, or local laws.
If you reside in the State of California, please also refer to Penumbra's Privacy Notice for California Residents.
For additional information on Penumbra’s commitment to being an equal opportunity employer, please Penumbra's AAP Policy Statement.