Strategic Scientific Advocate

Há 2 dias

Belo Horizonte MG, Brasil beBeeClinical Tempo inteiro

Medical Science Liaison Role We are seeking a skilled Medical Science Liaison to serve as a key scientific resource for stakeholders, clinical trial teams, and investigators. Clinical Trial Support Collaborate with clinical teams to optimize recruitment strategies and identify suitable patients. Engage with clinical sites and investigators to ensure smooth operations and alignment with study objectives. Provide education and training to clinical sites on study protocols and therapeutic areas. Insight Generation and Framework Creation Gather insights from healthcare professionals, patients, and other stakeholders to identify referral patterns, challenges, and opportunities. Develop frameworks to streamline patient identification and referral pathways. Stakeholder Engagement Build and maintain relationships with healthcare professionals, clinical trial investigators, and other key opinion leaders. Act as a liaison between clinical sites, investigators, and internal teams to ensure effective communication and support. Cross-Border Collaboration Work across national borders to address global clinical trial needs and ensure compliance with international regulations and cultural nuances. Collaborate with global teams to align on strategies and share best practices. Travel Requirements Travel extensively to meet with stakeholders, support trial sites, and attend relevant conferences and events. As a Medical Science Liaison, you will operate independently to manage responsibilities, meet deadlines, and drive projects forward while maintaining alignment with organizational goals. Your strong background in dermatology or rheumatology is essential for supporting clinical trials. You must also have experience working in cross-border settings and collaborating with global teams. Preferred candidates have an advanced degree in a relevant field and experience generating insights in dermatology or rheumatology clinical trials. Knowledge of global regulatory environments and best practices in clinical trial management is highly desirable.

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