
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
November 18

Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
• Lead planning and operational feasibility assessments to ensure realistic and achievable trial timelines • Oversee trial set-up and ensure team alignment across functions including Statistics, Data Management, Medical Writing, and Site Monitoring • Support country allocation and feasibility processes; provide input to optimize site selection and trial readiness • Develop and implement trial-level engagement, recruitment, and risk mitigation plans, integrating patient and site feedback to enhance trial design and participant experience • Coordinate outsourcing of vendor services, supporting vendor identification, selection, and scope-of-work development • Partner with cross-functional teams to ensure readiness across all trial processes — clinical quality, safety monitoring, investigational product management, budgeting, and site support • Facilitate and support responses to regulatory authorities, ethics committees, and other external stakeholders • Ensure all trial team members receive appropriate study-specific and standardized training • Maintain oversight of global clinical trial conduct to ensure compliance with Good Clinical Practice (GCP), internal SOPs, and all applicable regulatory requirements • Oversee patient recruitment progress, risk mitigation, and budget tracking to ensure efficient delivery • Manage amendments to study documentation and related retraining as needed • Ensure effective oversight of vendors and central labs, in collaboration with functional partners • Support ongoing communication and coordination across the clinical delivery network and stakeholders
• Bachelor’s degree (4-year undergraduate degree) in a relevant field • Proven experience leading Phase II & III global clinical trials • Therapeutic area experience in Immunology, Metabolic, or Oncology (additional TA experience is a plus) • Strong scientific and operational expertise across global clinical trial planning and execution • Exceptional leadership, communication, and stakeholder management skills in complex matrix structures • Ability to strategically plan and drive clinical trial delivery while ensuring patient-focused outcomes
• Health benefits to include Medical, Dental and Vision • Company match 401k • Eligibility to participate in Employee Stock Purchase Plan • Eligibility to earn commissions/bonus based on company and individual performance • Flexible paid time off (PTO) and sick time
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