# CTM II - Sr CTM assigned to client LAtam (USA scope or local scope)

**Company**: Syneos Health
**Work arrangement**: remote
**Experience**: senior
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ARG-Remote/CTM-II---Sr-CTM-assigned-to-client-LAtam--USA-scope-_25107944?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_a535445c-eb6

## Description

Syneos Health is seeking a CTM II - Sr CTM assigned to client LAtam (USA scope or local scope). The successful candidate 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:

- Oversees site interactions post-activation through site closeout

- Identifies critical data and processes, protocol execution risks, and risk mitigations

- Reviews study scope of work, budget, and protocol content

- Uses prior clinical experience, operational data, metrics, and reports to identify risks

- Escalates risks to clinical trial management deliverables to the project manager

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

- Participates and presents in key meetings

- Serves as an escalation point for communications with investigator site staff

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

- Develops and maintains clinical study tools and templates

- Coordinates initial and ongoing training to the study team

- Oversees resourcing allocations for CRAs and Central Monitors

- Ensures quality of clinical monitoring, central monitoring, and site management deliverables

- Reviews project oversight dashboards and other clinical trial systems

- Understands the monitoring strategy required for the study and participates in the development of the study risk assessment plan

- Reviews content and quality of site and central monitoring documentation

- Interacts with the client and other functional departments related to clinical monitoring, central monitoring, and site management activities

- Demonstrates understanding of other functions' roles in achieving compliance and delivery

- Oversees CRAs and Central Monitors assigned to the study

- 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 the achievement of project milestones

- Demonstrated capability of working in an international environment

- Demonstrated expertise in site management and monitoring

- Preferred experience with risk-based monitoring

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

- Must demonstrate good computer skills

- Good communication, presentation, and interpersonal skills

- Strong conflict resolution skills

- Demonstrated ability to apply problem-solving techniques to resolve complex issues

- Critical thinking to determine the cause and appropriate solution in the identification of issues

- Moderate travel may be required, approximately 20%

## Skills

### Required
- Clinical trial management
- Site management
- Monitoring
- Risk-based monitoring
- Good Clinical Practice
- ICH Guidelines
- Regulatory compliance
- Data integrity
- Patient safety
- Protocol compliance

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ARG-Remote/CTM-II---Sr-CTM-assigned-to-client-LAtam--USA-scope-_25107944?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)