Serving as a value-added resource and extension of the Company the Clinical Trial Liaison (CTL) will support the company's Ophthalmology pipeline. The CTL supports the execution of country medical plans related to clinical trial engagements. The CTL will work full time to educate, analyze, and resolve issues with clinical research sites and investigators.
This role involves compliant collaboration with KOLs, investigators, research staff members, advocacy groups to build strong professional partnerships, provide credible scientific expertise, and serve as a field-based extension to support the company's clinical trial programs.
ESSENTIAL DUTIES AND RESPONSIBILITIES
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 R&D 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
2+ years experience in a field clinical trial operations, design, site support and scientific engagement with clinical trial sites required
General Ophthalmology or Anterior segment ophthalmology therapeutic area experience required, Neurology a plus
Fluency in English and local language in country of residence 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
The Medical Affairs Company (TMAC) is one of the world’s leading outsourced medical affairs solutions providers that partners with biopharmaceutical, diagnostic, and medical device companies to establish or augment their medical affairs capabilities, helping treatments reach patients faster.
Our depth of industry knowledge and strong track record of over 25 years advances medical affairs as a strategic pillar in driving healthcare forward. Our innovative ecosystem offers quality solutions to make the commercialization process more efficient, compliant, and agile.
Every day we prioritize partnerships. With Relationships First as the cornerstone of our approach, we know that connections are paramount to success. This approach has earned our culture and processes recognition as we seek to empower through knowledge, advance healthcare, and enrich patients’ lives.
We’re a passionate team of medical affairs experts who will provide you with comprehensive solutions tailored to your lifecycle needs. To learn more visit www.TheMedicalAffairsCompany.com
