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Associate Safety Physician(m/w/x)
Managing product safety data and medical reviews for cancer/infectious disease treatments. MD with 2-3 years clinical/pharma experience required. Equal-Pay certified workplace.
Requirements
- MD with 2-3 years clinical/pharma experience or Physician with research fellowship
- Proven ability in medical review, data analysis, safety surveillance
- Solid understanding of GCP and PV principles
- Excellent English verbal and medical writing skills
- Thrive in high-stress matrix environment, collaborate effectively
- Strong problem-solving skills, meet deadlines, maintain quality
- Master's Degree
- Associate level experience
Tasks
- Manage and evaluate product safety data
- Manage project safety profiles
- Conduct individual and aggregate medical reviews
- Provide medical input for study protocols
- Provide medical input for Investigator Brochures
- Provide medical input for Development Safety Update Reports
- Lead ongoing safety monitoring
- Lead signal detection
- Partner with Clinical teams
- Partner with Regulatory teams
- Partner with Biostatistics teams
- Represent Safety in study teams
- Represent Safety in internal task forces
- Represent Safety in external meetings
- Contribute to safety sections of IND/NDA submissions
- Maintain inspection readiness for audits
- Maintain inspection readiness for inspections
Work Experience
- 2 - 3 years
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Benefits
Informal Culture
- Inclusive and respectful workplace
Competitive Pay
- Equal-Pay certified
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Associate Safety Physician(m/w/x)
Managing product safety data and medical reviews for cancer/infectious disease treatments. MD with 2-3 years clinical/pharma experience required. Equal-Pay certified workplace.
Requirements
- MD with 2-3 years clinical/pharma experience or Physician with research fellowship
- Proven ability in medical review, data analysis, safety surveillance
- Solid understanding of GCP and PV principles
- Excellent English verbal and medical writing skills
- Thrive in high-stress matrix environment, collaborate effectively
- Strong problem-solving skills, meet deadlines, maintain quality
- Master's Degree
- Associate level experience
Tasks
- Manage and evaluate product safety data
- Manage project safety profiles
- Conduct individual and aggregate medical reviews
- Provide medical input for study protocols
- Provide medical input for Investigator Brochures
- Provide medical input for Development Safety Update Reports
- Lead ongoing safety monitoring
- Lead signal detection
- Partner with Clinical teams
- Partner with Regulatory teams
- Partner with Biostatistics teams
- Represent Safety in study teams
- Represent Safety in internal task forces
- Represent Safety in external meetings
- Contribute to safety sections of IND/NDA submissions
- Maintain inspection readiness for audits
- Maintain inspection readiness for inspections
Work Experience
- 2 - 3 years
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Benefits
Informal Culture
- Inclusive and respectful workplace
Competitive Pay
- Equal-Pay certified
About the Company
Debiopharm
Industry
Pharmaceuticals
Description
Debiopharm is a privately-owned Swiss biopharmaceutical company committed to research in oncology and infectious diseases to improve patient outcomes and quality of life.
Not a perfect match?
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