# Clinical Trial Manager - Full Service

**Company**: Syneos Health
**Experience**: senior
**Job type**: full-time
**Salary**: The base salary range represents the anticipated low and high of the Syneos Health range for this position.
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-NC-Remote/Clinical-Trial-Manager---Full-Service_25110988?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_bc508ceb-32f

## Description

Syneos Health is seeking a Clinical Trial Manager - Full Service. As a Clinical Trial Manager, you will be responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance, and data integrity.

Responsibilities:

- Oversee site interactions post-activation through site closeout, including patient recruitment, investigator payments, and other related activities.

- Review study scope of work, budget, and protocol content, ensuring the clinical project team is aware of contractual obligations and parameters.

- Employ strategic thinking and problem-solving skills to propose and implement risk mitigations.

- Serve as an escalation point for communications with investigator site staff.

- Collaborate with other functional leaders to coordinate delivery handoffs and meet expected study milestones.

- Develop and maintain clinical study tools and templates, including the Clinical Monitoring Plan.

- Coordinate training for the study team regarding protocol specificities, Case Report Form completion, and Sponsor Standard Operating Procedures.

- Oversee resourcing allocations for CRAs and Central Monitors, site assignments, and study team members' conduct.

- Review project oversight dashboards and other clinical trial systems to ensure data has been updated to reflect timely execution of all operational aspects.

- Understand the monitoring strategy required for the study and participate in the development of the study risk assessment plan.

- Review content and quality of site and central monitoring documentation.

- Interact with clients and other functional departments related to clinical monitoring, central monitoring, and site management activities and deliverables.

- Demonstrate understanding of other functions' roles in achieving compliance and delivery according to protocol, SOPs, ICH GCP, and country regulations.

- Oversee CRAs and Central Monitors assigned to the study and assess study-specific process and training compliance.

- Provide 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 the achievement of project milestones.

- Demonstrated capability of working in an international environment.

- Demonstrated expertise in site management and monitoring (clinical or central).

- Preferred experience with risk-based monitoring.

- Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.

- Strong conflict resolution skills.

- Moderate travel may be required, approximately 20%.

## Skills

### Required
- Good Clinical Practice
- ICH Guidelines
- Risk-Based Monitoring
- Site Management
- Clinical Monitoring
- Central Monitoring
- Protocol Development
- Budget Management
- Conflict Resolution

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-NC-Remote/Clinical-Trial-Manager---Full-Service_25110988?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)