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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates advanced knowledge of glaucoma and ophthalmic surgical procedures, with proven experience in clinical trial design, regulatory requirements, and scientific communication. Capable of developing peer-to-peer relationships with medical experts while ensuring compliance with GxP regulations and industry standards.
Highest-signal resume keywords
Advanced Knowledge Of GlaucomaClinical Trial DesignRegulatory RequirementsScientific PresentationsMedical Writing
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 DesignMedical WritingBiostatisticsOphthalmic Surgical ProceduresEvidence-Based Scientific ExchangeAdverse Event ReportingProduct DevelopmentRegulatory SubmissionsQuality ControlGCP Compliance
Soft Skills
Peer-To-Peer Relationship DevelopmentCommunication SkillsProblem-Solving
Certifications & Qualifications
MDOD
Industry Keywords
OphthalmologyOptometryECP-Facing RoleHealthcare SystemICH GuidelinesGxP RegulationsSOPsQuality AssuranceMarket AccessLife Cycle Management
Tech Stack
Tools & technologiesGoogle Cloud Platform
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 and gather external insights
- Provide general medical information to practitioners and Alcon associates and 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
- Maintain thorough knowledge of Alcon products and current medical/scientific research
- Work with Medical Information and Medical 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, monitor protocol adherence, and determine study completion
- Provide reporting information for submissions to regulatory agencies
- Serve as medical consultant to marketing, commercial, research, and regulatory teams and licensing-agreement corporations
- Sign off on product safety reviews
- Interface with Medical Affairs and Commercial, Quality Assurance, Research and Development, Regulatory Affairs, and Market Access departments
- Follow laws, industry standards, company policies, GxP regulations, SOPs, documentation, quality control, and required training
Requirements
What you’ll need- Bachelor’s Degree or equivalent years of directly related experience
- Alternative experience equivalencies: high school + 15 years; Associate degree + 11 years; M.S. + 4 years; PhD + 3 years
- Fluent ability to read, write, understand and communicate in English
- 7 years of relevant experience
- Advanced knowledge of glaucoma, including ophthalmic surgical procedures and optometry
- Experience in an ophthalmology or optometry field, including ophthalmic industry or clinical practice
- Experience in an ECP-facing role
- Working knowledge of the healthcare system, research procedures, ICH guidelines, GCP, and other ethical guidelines
- Knowledge of clinical trial design, product development, regulatory requirements, payer landscape, and life cycle management
- Experience in scientific presentations, medical writing, and biostatistics
- Proven ability and experience developing and fostering peer-to-peer relationships with medical experts and decision makers
- Ability to comply with GxP regulations, SOPs, documentation, quality control, training, laws, industry standards, and company policies
- MD or OD with specialization in Ophthalmology (preferred)
Benefits
Comp & perks- Health benefits
- Life benefits
- Retirement benefits
- Flexible time off
