The Medical Science Liaison is a key role in our organization, requiring a professional with a strong background in dermatology or rheumatology.
Job Description
This position involves collaborating with clinical trial teams to support trial enrollment efforts, including identifying suitable patients and optimizing recruitment strategies. The successful candidate will serve as a scientific resource, building relationships with stakeholders, facilitating clinical trial activities, and generating insights to inform strategy and improve patient outcomes.
Key Responsibilities:
* Clinical Trial Support: Collaborate with clinical trial teams to support trial enrollment efforts, including identifying suitable patients and optimizing recruitment strategies.
* Insight Generation and Framework Creation: Gather and synthesize insights from healthcare professionals (HCPs), patients, and other stakeholders to identify referral patterns, challenges, and opportunities for trial enrollment.
* Stakeholder Engagement: Build and maintain relationships with HCPs, clinical trial investigators, and other key opinion leaders (KOLs) in dermatology.
Requirements
To be successful in this role, you should have:
* A minimum of 3 years of experience as a Medical Science Liaison or in a similar role.
* A strong background in dermatology or rheumatology, with experience engaging with dermatologist-focused clinical trial sites and investigators.
* Proven track record of supporting clinical trial enrollment, patient identification, and site engagement.
Benefits
This role offers the opportunity to work autonomously, manage responsibilities, and drive projects forward while maintaining alignment with organizational goals. You will also have the chance to travel extensively, collaborate with global teams, and engage with diverse stakeholders.
Preferred qualifications include an advanced degree in a relevant field and experience with insight generation in the context of dermatology or rheumatology clinical trials. Knowledge of global regulatory environments and best practices in clinical trial management is also desirable.