Clinical Medical Advisor

🔥 9 minutes ago

🇰🇷 South Korea – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✨ Clinical Advisor

👻 Ghost score 10%

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Provide country-level and/or global clinical and medical leadership for selected trials • Validate study designs and feasibility and contribute to protocol development • Use competitive intelligence and real-world data to inform recruitment strategies and trial planning • Ensure adherence to GCP/ICH and regulations • Review study documents, safety findings, and protocol deviations • Collaborate with internal and external stakeholders to meet project milestones and timelines • Identify barriers and implement mitigation strategies • Gather and communicate clinical/medical insights to optimize trial execution and inform strategy • Deliver medical/scientific education and provide input on clinical trial training materials • Represent Clinical Development and Medical Affairs at meetings, advisory boards, and scientific forums • Oversee complex, multi-country, or high-visibility trials as a senior clinical leader • Drive global clinical strategy contributions and influence study design, operational feasibility, country/site strategy, and evidence-generation approaches • Interpret safety findings, data irregularities, protocol deviations, and risk indicators • Act as a clinical strategist and decision influencer for internal teams and external partners • Mentor Clinical Trial Scientist I and II team members and train investigators, regional partners, or cross-functional colleagues • Represent the organization as a subject-matter expert in scientific and regulatory-interaction forums • Lead high-complexity issue resolution involving recruitment, feasibility, and regulatory constraints • Contribute to portfolio-level planning, program feasibility, scientific trends, and competitive intelligence assessments

🎯 Requirements

• Clinical and medical expertise for country-level and/or global clinical leadership • Knowledge of GCP/ICH and applicable regulations • Ability to validate study designs and feasibility and contribute to protocol development • Ability to leverage competitive intelligence and real-world data for recruitment strategies and trial planning • Experience collaborating with Clinical Operations, CROs, Medical Affairs, Regulatory, Pharmacovigilance, and site staff • Ability to interpret safety findings, data irregularities, protocol deviations, and risk indicators • Ability to develop risk-mitigation strategies and lead cross-functional clinical risk reviews • Ability to guide scientific direction, program risk tolerance, and clinical best practices • Ability to mentor Clinical Trial Scientist I and II team members • Ability to address global recruitment challenges, feasibility barriers, and country-specific regulatory constraints • Equivalent experience, skills, and/or education will be considered

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Total Self culture • Diversity, inclusion, and belonging initiatives • Reasonable accommodations when appropriate