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Job Summary
Generate and translate clinical evidence into value propositions, usage algorithms, and clinical‑economic arguments that facilitate adoption across Clinical, Marketing, and Commercial functions, applying strong methodological rigor and a patient‑centric approach
Key Accountabilities
- Assess the diagnostic impact in CTD of four different algorithms/workflows (IFA versus Aptiva solid‑phase technology).
- Identify and address unmet needs in myositis diagnostics, transitioning from low‑confidence blot assays to quantitative Aptiva testing with improved sensitivity and specificity.
- Evaluate the clinical impact of using dsDNA testing on Aptiva for diagnosis and BIO‑FLASH for patient monitoring, leveraging two complementary technologies/platforms.
- Work collaboratively with Business Unit Product Managers, Clinical Specialists, R&D, and the Business Unit Manager to deliver actionable outcomes.
Networking/Key relationships
• Product Managers
• SAS
• Clinical Specialist
• SBU and R&D
• KOL/Immunologists
• Compliance / Regulatory / Legal
Minimum Knowledge:
• Education: Biology/Biochemestry, Chemistry, or Biotech.
• Language:
- Spanish and English fluent
- Portuguese desirable
Skills & Capabilities:
- Proactive and organized, with a focus on improving daily processes.
- Proficient in Microsoft Office (especially Excel, Word, and PowerPoint).
- Comfortable working with data and repetitive tasks with attention to detail.
- Curious and willing to learn about products, customers, and the market.
- Team-oriented, with a positive attitude and eagerness to contribute.
- Critical appraisal of scientific literature, evidence synthesis, and structured analysis, supported by a strong biomedical background and hands‑on experience in hospital‑based research.
- Medical–Marketing interface mindset, with the ability to communicate scientific information effectively to diverse stakeholders.
