Sr CTM (Clinical trial medical Advisors)

📋 Description

• • Syneos Health is seeking a Senior Clinical Trial Medical Advisor (Sr CTM) to join our dynamic team, focusing on accelerating customer success within the biopharmaceutical solutions sector.
• • This is a field-based, scientific role designed to foster robust relationships with Key Opinion Leaders (KOLs) and reinforce critical scientific messaging throughout clinical trials.
• • As an individual contributor, you will be instrumental in supporting assigned programs, assets, and indications, playing a key role in the execution of Global Clinical Development Strategies.
• • You will ensure the scientific integrity and consistency of messaging across multiple studies, ensuring that protocol execution principles are upheld.
• • A significant aspect of this role involves extensive external stakeholder engagement, requiring travel to investigator sites as needed to support territory and site-specific requirements.
• • Your primary focus will be on Scientific Investigator Engagement, building and maintaining credible, compliant relationships with Principal Investigators (PIs), Sub-Investigators (Sub-Is), and other key study physicians.
• • You will provide high-quality scientific exchange, offering support on study rationale, objectives, endpoint rationale, assessment methodologies, and operational feasibility.
• • A crucial part of your responsibility is to provide scientific support for protocol implementation, reinforcing the understanding of critical-to-quality elements such as endpoint assessments, timing windows, safety evaluations, and key procedures.
• • You will proactively identify recurring points of confusion or variability in areas like screening failures, inclusion/exclusion criteria, and endpoint consistency, and communicate these themes to internal teams to drive targeted training and clarification materials.
• • When scientifically appropriate and within defined role boundaries, you will assist in troubleshooting site-level scientific implementation barriers, coordinating follow-up with the relevant internal stakeholders.
• • The role also involves contributing to Trial Feasibility, Enrollment, and Retention Science by providing scientifically grounded input derived from discussions with investigators regarding patient flow, referral patterns, community advocacy, and competitive trial landscapes.
• • You will collaborate with study and country operational leads (e.g., CTM/CRA) to inform recruitment and retention strategies, ensuring alignment while maintaining your focus on scientific execution readiness.
• • A key function is to capture and synthesize structured investigator insights on protocol burden, physician perspectives, endpoint relevance, operational challenges, and evolving practice patterns that may impact study conduct.
• • These insights will be communicated in an action-oriented format to support decision-making, highlighting clarification needs, key risk themes, training opportunities, and potential improvements for future protocol designs or amendments.
• • You will actively support the scientific components of investigator meetings and site engagement forums, contributing to content, preparing for scientific Q&A, and aligning key messages.
• • You may be required to deliver formal scientific presentations, such as protocol deep-dives or endpoint rationale, adhering to governance expectations.
• • Attendance at relevant scientific and clinical meetings or congresses is expected to maintain scientific currency, understand evolving clinical trends, and support investigator relationships within your remit and in compliance with regulations.
• • You must operate with a strong commitment to compliance, adhering to ICH/GCP guidelines and company Standard Operating Procedures (SOPs).
• • Scientific exchanges must remain appropriate, non-promotional, study-governed, and respect blinding and data access rules.
• • Maintaining complete and timely documentation of external interactions, insights, and follow-ups in required systems is essential, tracking activity and outcomes per team expectations.
• • You will be responsible for escalating scientific risks, trends, or protocol execution signals appropriately to ensure inspection readiness and maintain study quality.
• • Prompt reporting of any adverse events, product complaints, or safety concerns encountered in the field through established processes is mandatory.
• • This role requires managing an assigned geography or territory from a home-based office, with the flexibility to travel to investigator sites as needed.
• • You will engage with external stakeholders including PIs, Sub-Is, study physicians, study coordinators, site decision-makers, research leadership, and advocacy groups.
• • Internal collaboration will be with Clinical Science/Clinical Development leadership, study teams, country/study operational leads, and partners in Regulatory, Quality, and Drug Safety.