Syneos Health
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.
Country Operations Associate I
🔥 0 minutes ago
📊 Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
Syneos Health
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 operational support across the full site lifecycle: Start-Up, Conduct, and Close-Out • Act as a key contact between clinical teams, investigator sites, CROs, and external partners • Support Regulatory Authority and Ethics Committee submissions and associated documentation • Prepare and maintain Investigator Initiation Packages and essential study documents • Perform document management activities in PTMF, eISF, CTMS, and document exchange systems • Support site contracting and budget processes, including tracking negotiations and execution status • Maintain study trackers, timelines, and task status to ensure visibility of risks and progress • Review study and site files for completeness and support TMF/eISF reconciliation activities • Contribute to quality, inspection readiness, compliance, and continuous improvement initiatives in accordance with ICH/GCP and local regulations
🎯 Requirements
• Requires 2-5 years of experience in site activation, clinical trial support, or clinical operations • Strong organizational and communication skills • BS/BA or bachelor’s degree in life sciences or a related discipline is an asset • Knowledge of ICH/GCP and local regulations • Equivalent experience, skills, and/or education may be considered
🏖️ Benefits
• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Comprehensive resources including emerging technologies, data, science and knowledge sharing • Diverse career paths and employment opportunities
Apply Now
