Full-Time
Associate Manager
Confirmed live in the last 24 hours
Develops healthcare technologies for vascular conditions
Compensation Overview
$107,064 - $167,911Annually
Mid
Alameda, CA, USA
- 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.
- Collaborate with market access team to clarify and finalize user requirement specifications for market access data analysis tools and reports.
- 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
Penumbra, Inc. excels in pioneering healthcare technologies specifically designed for neuro and peripheral vascular conditions. This involves a focus on stroke revascularization and embolization, with leading products like the REAL Immersive System and ACE Reperfusion Catheters that underline their commitment to top-tier, patient-focused innovations. Their dedication to leveraging cutting-edge technology in medical solutions makes it an outstanding workplace for professionals eager to impact critical care positively and advance in the fast-evolving healthcare sector.
Company Stage
IPO
Total Funding
$3.4M
Headquarters
Alameda, California
Founded
2004