Medical Science Liaison-Central Region
Harrow
20 days ago
On-site
Texas, United States
Medical Affairs
Territory: Dallas, Houston, St. Louis, Indianapolis, and Chicago
MSL Summary
- Develop and maintain peer-to-peer relationships with Key Opinion Leaders (KOLs) in Ophthalmology and Optometry.
- Support development and appropriate use/adoption of Harrow products through evidence-based scientific exchange and external insights.
- Provide general medical/healthcare information to practitioners and internal associates.
- Respond to unsolicited requests for medical information, scientific exchange/insights, research, and publications.
- Ensure timely, compliant, customer-focused dissemination of clinical/scientific information; support authorship of scientific materials.
Accountabilities
- Medical support and KOL relationship development; provide up-to-date medical guidance tied to guidelines/evidence.
- Provide non-promotional speaker training to HCPs.
- Identify KOLs; develop peer-to-peer relationships; secure advocacy.
- Serve as interface between Medical Expert/HCP and Harrow; escalate to Medical Affairs as needed.
- Present as medical speaker at sites/training events.
- Collect/analyze/report field insights impacting trials, launch, and strategy.
- Support and author scientific assets (presentations, papers, abstracts, manuscripts, materials).
- Support clinical trial KOL involvement; liaise on Investigator Initiated Trials (IITs) from inception to publication.
- Contribute to medical strategy; implement/support US Medical Affairs-aligned projects.
- Provide disease-state/product medical support and training to colleagues (not a substitute for functional training groups).
- Work with Med Info and Med Safety to resolve escalated complaints and safety issues.
- Interface with Medical Affairs and other departments (Commercial, QA, Regulatory, Market Access, etc.).
- Ensure integrity/compliance and complete required healthcare institution credentialing.
Preferred Qualifications
- Terminal Degree required: MD/DO/OD/PhD/PharmD.
- Ophthalmology experience required.
- 5+ years in a Medical Science Liaison role with progressive responsibilities.
- Clinical trial design/execution experience.
- Scientific presentation experience.
- Knowledge of product development, clinical trial design, regulatory requirements, payer landscape, life cycle management.
- Working knowledge of healthcare system/research procedures; ICH, GCP, and ethical guidelines.
- Proven ability to build peer-to-peer relationships with medical experts/decision makers.
- English fluency (read/write/communicate).
- Travel: 60–70%; must live within a 30-minute commute to a major airport.
MSL Summary
- Develop and maintain peer-to-peer relationships with Key Opinion Leaders (KOLs) in Ophthalmology and Optometry.
- Support development and appropriate use/adoption of Harrow products through evidence-based scientific exchange and external insights.
- Provide general medical/healthcare information to practitioners and internal associates.
- Respond to unsolicited requests for medical information, scientific exchange/insights, research, and publications.
- Ensure timely, compliant, customer-focused dissemination of clinical/scientific information; support authorship of scientific materials.
Accountabilities
- Medical support and KOL relationship development; provide up-to-date medical guidance tied to guidelines/evidence.
- Provide non-promotional speaker training to HCPs.
- Identify KOLs; develop peer-to-peer relationships; secure advocacy.
- Serve as interface between Medical Expert/HCP and Harrow; escalate to Medical Affairs as needed.
- Present as medical speaker at sites/training events.
- Collect/analyze/report field insights impacting trials, launch, and strategy.
- Support and author scientific assets (presentations, papers, abstracts, manuscripts, materials).
- Support clinical trial KOL involvement; liaise on Investigator Initiated Trials (IITs) from inception to publication.
- Contribute to medical strategy; implement/support US Medical Affairs-aligned projects.
- Provide disease-state/product medical support and training to colleagues (not a substitute for functional training groups).
- Work with Med Info and Med Safety to resolve escalated complaints and safety issues.
- Interface with Medical Affairs and other departments (Commercial, QA, Regulatory, Market Access, etc.).
- Ensure integrity/compliance and complete required healthcare institution credentialing.
Preferred Qualifications
- Terminal Degree required: MD/DO/OD/PhD/PharmD.
- Ophthalmology experience required.
- 5+ years in a Medical Science Liaison role with progressive responsibilities.
- Clinical trial design/execution experience.
- Scientific presentation experience.
- Knowledge of product development, clinical trial design, regulatory requirements, payer landscape, life cycle management.
- Working knowledge of healthcare system/research procedures; ICH, GCP, and ethical guidelines.
- Proven ability to build peer-to-peer relationships with medical experts/decision makers.
- English fluency (read/write/communicate).
- Travel: 60–70%; must live within a 30-minute commute to a major airport.