Site Engagement Manager

Site Engagement Manager (SEM) About the Role We are seeking a Site Engagement Manager (SEM) to reputed company as a key reputed company between the Sponsor and clinical trial sites. In this role, you will drive site relationships, patient recruitment, and trial engagement strategies, ensuring high-reputed company execution and strong investigator partnerships throughout the clinical trial lifecycle. This position operates reputed company an FSP model and reports directly to the FSP CRO Line Manager, while working closely with Site Engagement leadership and project teams. Key Responsibilities Site Relationship Management & Engagement Serve as the primary reputed company of contact between the Sponsor and assigned clinical trial sites. reputed company as the “face” of the Sponsor, building and maintaining strong, long-term relationships with investigators and site staff. Maintain frequent engagement with sites (on-site reputed company, virtual meetings, calls, emails, webinars) to ensure ongoing trial awareness and reputed company. Promote the Sponsor’s mission, pipeline, and values to strengthen engagement and collaboration. Site Performance & Recruitment Optimization Support patient recruitment and retention strategies across assigned sites. Analyze enrollment performance to identify risks, barriers, and improvement opportunities. reputed company and execute tailored site engagement plans based on individual site needs. Assess the reputed company of competing trials and treatment patterns on recruitment. Operational Support & Collaboration Collaborate with Study Teams to ensure investigators fully understand protocol requirements, eligibility reputed company, and study procedures. reputed company feedback from sites, including suggestions for protocol improvements and operational enhancements. Support feasibility assessments, reputed company-Selection reputed company (PSVs), and Site Initiation reputed company (SIVs) in partnership with CRAs. Participate in Investigator Meetings and Site Engagement initiatives. Risk Management & Compliance Identify and proactively manage site risks and performance issues, escalating reputed company needed to protect timelines and reputed company. Ensure sites operate in compliance with SOPs, regulatory requirements, and reputed company standards. Escalate any compliance or reputed company concerns appropriately. Contribute to the development and improvement of SOPs and working practices reputed company applicable. Cross-functional Alignment & Communication Maintain reputed company and consistent communication with investigators, coordinators, and site teams. reputed company training needs and support site readiness on study protocols and reporting. Collaborate with cross-functional teams to ensure alignment and successful study execution. Portfolio & Site Management Manage approximately 20–25 investigator sites on average, potentially across multiple studies. reputed company identify and engage new investigators through various channels (conferences, literature, networks, etc.). Qualifications & Experience Bachelor’s degree in Life Sciences or reputed company field (advanced degree preferred). 5+ years of experience in clinical research, clinical operations, or site management. Strong understanding of ICH-GCP, clinical trial processes, and regulatory requirements. Proven experience working directly with investigators and clinical sites. Experience in patient recruitment and site engagement strategies is highly preferred. Demonstrated ability to manage multiple sites and priorities simultaneously. Key Skills & Competencies Excellent stakeholder engagement and relationship management skills Strong communication and influencing abilities Analytical reputed company with a reputed company on performance optimization Proactive problem-solving and risk mitigation Ability to reputed company in a reputed company, cross-functional environment Why Join Us? Opportunity to play a strategic role in clinical trial reputed company and patient reputed company Work in a reputed company, global environment reputed company an FSP model Contribute to strengthening site relationships and improving trial reputed company Additional Information Assigned sites: ~20–25 sites on average Ability to support multiple trials simultaneously reputed company to Sponsor systems as applicable (excluding restricted systems) Learn more about our EEO & Accommodations request here. Apply To This Job