Clinical Medical Advisor

This is a fully remote position, open to applicants in South Korea.

📋 Description

• Offer clinical and medical leadership at both country and global levels for selected trials.

• Assess study designs and feasibility while contributing to the development of protocols.

• Utilize competitive intelligence and real-world data to shape recruitment strategies and trial planning.

• Ensure compliance with GCP/ICH guidelines and regulatory requirements.

• Review study documentation, safety findings, and any deviations from protocols.

• Collaborate with both internal and external stakeholders to achieve project milestones and timelines.

• Identify obstacles and implement strategies for mitigation.

• Collect and communicate clinical and medical insights to enhance trial execution and inform strategic decisions.

• Provide medical and scientific education while contributing to clinical trial training materials.

• Represent Clinical Development and Medical Affairs at meetings, advisory boards, and scientific discussions.

• Oversee complex, multi-country, or high-visibility trials as a senior clinical leader.

• Drive contributions to global clinical strategy, influencing study design, operational feasibility, country/site strategy, and evidence-generation methods.

• Analyze safety findings, data inconsistencies, protocol deviations, and risk indicators.

• Serve as a clinical strategist and decision-maker for both internal teams and external partners.

• Mentor Clinical Trial Scientist I and II team members while training investigators, regional partners, or cross-functional colleagues.

• Act as a subject-matter expert in scientific and regulatory interaction forums for the organization.

• Lead resolution of high-complexity issues related to recruitment, feasibility, and regulatory challenges.

• Contribute to portfolio-level planning, program feasibility, scientific trends, and assessments of competitive intelligence.

⛳️ Requirements

• Expertise in clinical and medical fields for country-level and/or global clinical leadership.

• Knowledge of GCP/ICH and relevant regulations.

• Capability to validate study designs and feasibility while contributing to protocol development.

• Proficiency in leveraging competitive intelligence and real-world data for recruitment strategies and trial planning.

• Experience in collaboration with Clinical Operations, CROs, Medical Affairs, Regulatory, Pharmacovigilance, and site staff.

• Ability to interpret safety findings, data inconsistencies, protocol deviations, and risk indicators.

• Skills in developing risk-mitigation strategies and leading cross-functional clinical risk reviews.

• Ability to steer scientific direction, program risk tolerance, and clinical best practices.

• Capability to mentor Clinical Trial Scientist I and II team members.

• Skills to address global recruitment challenges, feasibility barriers, and country-specific regulatory constraints.

• Equivalent experience, skills, and/or education will be taken into consideration.

🏝️ Benefits

• Opportunities for career development and advancement.

• Supportive and engaged management team.

• Training in technical and therapeutic areas.

• Recognition among peers.

• Comprehensive total rewards program.

• Culture of total self.

• Initiatives promoting diversity, inclusion, and belonging.

• Reasonable accommodations provided when appropriate.