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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical trials, providing medical information, and ensuring compliance with GxP regulations. Capable of engaging with medical experts and influencing company strategies through evidence-based scientific exchange.
Highest-signal resume keywords
Clinical Trial ManagementMedical Information ProvisionGxP ComplianceAlcon Product KnowledgeAdverse Event Reporting
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial Protocol AdherenceRegulatory Submissions ReportingEvidence-Based Scientific ExchangeMedical Project ImplementationInvestigator Trial Navigation
Soft Skills
Relationship BuildingCommunicationProblem Solving
Industry Keywords
Medical AffairsQuality AssuranceRegulatory AffairsMarket AccessSOPs
About the role
Key responsibilities & impact- Develop and maintain peer-to-peer relationships with medical experts and key opinion leaders
- Support development and adoption of Alcon products through evidence-based scientific exchange
- Gather external insights to influence company strategies
- Provide general medical information to practitioners and Alcon associates
- Respond to unsolicited medical information requests
- Engage in scientific discussions about Alcon product data
- Implement medical projects and navigate investigator trials from inception to publication
- Work with Med Info and Med Safety to resolve escalated product complaints and medical safety issues
- Participate in adverse event reporting and safety responsibility monitoring
- Direct phase III and IV human clinical trials for products under development
- Monitor clinical trial protocol adherence and determine study completion
- Provide reporting information for regulatory agency submissions
- Serve as medical consultant to marketing, commercial, research, and regulatory teams
- Act as consultant/liaison with corporations under licensing agreements
- Sign off on product safety reviews
- Interface with Medical Affairs, Commercial, Quality Assurance, Research and Development, Regulatory Affairs, Market Access, and other departments
- Work with integrity and compliance while maintaining rigorous quality control and continuous improvement
Requirements
What you’ll need- Bachelor’s Degree or equivalent years of directly related experience
- Alternative qualification: high school + 15 years of experience
- Alternative qualification: Associate degree + 11 years of experience
- Alternative qualification: M.S. + 4 years of experience
- Alternative qualification: PhD + 3 years of experience
- 7 years of relevant experience
- Fluency in reading, writing, understanding, and communicating in English
- Ability to travel 75%
- Thorough knowledge of Alcon products and current medical/scientific research
- Compliance with GxP regulations, SOPs, laws, industry standards, and company policies
- Accurate and complete documentation
- Required training completion
Benefits
Comp & perks- Focused growth and development opportunities
- Health benefits
- Life insurance
- Retirement benefits
- Flexible time off
- Short-term incentive opportunities for eligible roles
- Long-term incentive opportunities for eligible roles
- Programs promoting health and well-being
- Financial security programs
- Retirement planning support
- Reasonable accommodation for individuals with disabilities