Site and Investigator Partnerships
- Create investigator engagement plans to support site identification and selection
- Build and maintain partnerships with potential PIs for company clinical trials
- Conduct compliant scientific exchange to educate on company clinical trials
- Provide clinical trial liaison support to site investigators involved in sponsored studies including protocol support, screening barriers, and clinical trial recruitment and retention
- Collection of key medical insights from PIs to inform refinement of strategies
- Serve as a liaison to internal RD functions to ensure the effective support of PIs
- Respond in a timely manner to unsolicited inquiries from external stakeholders and HCPs
Building Company Pipeline Advocacy
- Through compliant scientific exchange, build and maintain professional relationships with external stakeholders to expand research, company advocacy, and educational partnerships
- Collect key strategic insights from top research KOLs and HCPs to support strategic initiatives
- Support execution of strategy through creation of national and regional congress plans for your assigned territories to attend and execute activities
Qualifications
- An advanced degree in life sciences (MD, PharmD or PhD or equivalent) required
- Has established scientific relationships and the ability to deliver effective presentations to HCPs
- Experience in clinical trial operations, design, site support and scientific engagement with clinical trial sites required.
- General Ophthalmology or Anterior segment ophthalmology therapeutic area experience required
- At least 2 years of therapeutic, research or substantive patient care experience is required
- Frequent travel is required. Availability to travel up to 75% of time
- Availability to attend meetings on holidays and weekends
- Ability to travel internationally as needed with valid passport
- Clean and valid driver’s license
pTerritory will include mu
📌 Clinical Trial Liaison (Lodi)
🏢 The Medical Affairs Company (Tmac)
📍 Lodi
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