Manager, Biospecimen Reporting and Automation

• Accountable for creation of automation and maintenance of standard reporting suite.
• Accountable for development of dashboards (SLA adherence, discrepancy trends, shipment health, pending analysis, study health).
• Accountable for backend query development (SQL) and script automation (Python or equivalent).
• Accountable for validation and version control of reporting logic and templates.
• Accountable for Back Office Study Health Pack production (KPIs, exceptions, action recommendations).
• Accountable for cross-TA KPI insights and QBR-ready performance analytics.
• Accountable for automation change control lifecycle (requirements → build → test → validation → release → monitoring).
• Accountable for reducing manual data pulls and improving data reliability.
• Accountable for master reporting governance and data lineage traceability.

Competencies

• Advanced SQL querying and data modeling capability.
• Proficiency in Python or similar programming language.
• BI platform expertise (Power BI, Tableau, equivalent).
• Strong understanding of relational data structures and interface dependencies.
• Knowledge of validation frameworks in regulated environments.
• Ability to translate operational processes into scalable automation.
• Data visualization and executive-level insight synthesis.
• Continuous improvement and digital-first mindset.

Qualifications

  The knowledge and skills necessary to perform the duties of this position are typically acquired through the following combination of education, experience and knowledge, or the equivalent.

Minimum Requirements

•Doctorate degree

OR

•Master’s degree & 3 years of experience in supplier management at sponsor or supplier leadership at the vendor

OR

•Bachelor’s degree & 5 years of experience in supplier management at sponsor or supplier leadership at the vendor

OR

•Associate’s degree and 10 years of experience in supplier management at sponsor or supplier leadership at the vendor

AND

•Strong project management experience

•Fluency in English, both in written and oral communication

•Excellent user of Office Programs such as Excel, Word, Power point

•Scientific or drug development technical expertise supporting Research, Development, Medical, Global Regulatory, Global Safety or Knowledge Management

Preferred Requirements

•7 years work experience in life sciences field, including 4 years of biopharmaceutical R&D experience

•Functional experience managing oversight of R&D suppliers (CROs, specialty labs, imaging suppliers, etc.)

•Experience working in a global, matrix organization

EQUAL OPPORTUNITY STATEMENT 

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. 

We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.