[Hiring] Clinical Trial Manager II / Vendor Manager @Syneos Health

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description This role involves managing clinical trials and vendor relationships with a focus on patient safety, compliance, and data integrity. • Responsible for site management oversight, clinical monitoring, and central monitoring deliverables. • Oversees site interactions post-activation through site closeout, including patient recruitment and investigator payments. • Identifies critical data and process risks and mitigations related to protocol execution. • Reviews study scope of work, budget, and protocol content to ensure compliance with contractual obligations. • Uses clinical experience and operational data to identify risks to clinical trial management deliverables. • Escalates risks to project manager regarding timeline, quality, and budget. • Employs strategic thinking and problem-solving skills to propose and implement risk mitigations. • Participates and presents in key meetings such as Kick Off Meetings. • Serves as an escalation point for communications with investigator site staff. • Collaborates with functional leaders to coordinate delivery handoffs and meet study milestones. • Responsible for development and maintenance of clinical study tools and templates. • Coordinates training for the study team on protocol specifics and clinical plans. • Oversees resource allocations for CRAs and Central Monitors. • Ensures quality of clinical monitoring and site management deliverables. • Reviews project oversight dashboards and clinical trial systems to ensure timely execution of operational aspects. • Understands monitoring strategy and participates in developing study risk assessment plans. • Reviews site and central monitoring documentation for compliance and quality. • Interacts with clients and other departments regarding clinical monitoring activities. • Demonstrates understanding of other functions' roles in achieving compliance and delivery. • Oversees CRAs and Central Monitors, assessing compliance and identifying risks. • Provides feedback to line managers on staff performance. Qualifications • Bachelor’s degree or RN in a related field or equivalent combination of education, training, and experience. • Demonstrated ability to lead and align teams in achieving project milestones. • Experience working in an international environment. • Expertise in site management and monitoring (clinical or central). • Preferred experience with risk-based monitoring. • Understanding of clinical trial management financial principles and budget management. • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements. • Good computer skills. • Strong communication, presentation, and interpersonal skills. • Strong conflict resolution skills. • Ability to apply problem-solving techniques to resolve complex issues. • Critical thinking skills to determine causes and solutions for issues. • Moderate travel may be required, approximately 20%. Benefits • Company car or car allowance. • Health benefits including 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. Salary Range $95,000.00 - $175,700.00 The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. Apply tot his job