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Associate Consultant at Michael Page
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Medical Affairs Manager - Medical Devices (6-10 yrs)
- Medical subject expert and resource on medical, scientific, technical and therapeutic areas supporting medical sciences' objectives and strategies.
- Contributes medical relevance to risk assessments and quality risk management reviews, analyses and processes such as FMEAs, DFUs, CRBA/CESs, MESL, PIRs, HHAs, Has and CAPAs.
- Conducts exploratory analyses of medical data and data extraction collaborating with Business heads, clinical, global medical safety, quality and product development teams.
- Authors and conducts literature reviews, multilevel in-depth medical analyses, white papers, medical / disease educational materials, summaries for strategy and documentation.
- Medical expert and liaison across all business units and functions including but not limited to clinical, regulatory, quality, research and development, legal, global medical safety and post market surveillance.
- Participates as contributor and reviewer of clinical research protocols and documentation (including but not limited to ICFs, CRFs, safety plans), study reports and statistical analysis plans.
- Serve as a representative to leadership boards and committees as requested. Fully trained as per QA training compliance for representation.
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