# Site Care Partner (Sponsor dedicated) - Buenos Aires only

**Company**: Syneos Health
**Location**: Buenos Aires
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ARG-Remote/Site-Care-Partner--Sponsor-dedicated----Buenos-Aires-only---Min-6--years-of-previous-monitoring-experience--ideally-in-Oncology-_25112421?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_bf73ac6c-abf

## Description

Syneos Health is seeking a Site Care Partner (Sponsor dedicated) to work in Buenos Aires. The successful candidate will have a minimum of 6 years of previous monitoring experience, ideally in Oncology.

The Site Care Partner will perform site qualification, site initiation, interim monitoring, site management, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance. They will use judgment and experience to evaluate the overall performance of the site and site staff and provide recommendations regarding site-specific actions.

Key responsibilities include:

- Performing site qualification, site initiation, interim monitoring, site management, and close-out visits

- Evaluating overall performance of site and site staff and providing recommendations

- Verifying the process of obtaining informed consent has been adequately performed and documented

- Assessing factors that might affect subject/patient's safety and clinical data integrity

- Conducting Source Document Review of site source documents and medical records

- Applying query resolution techniques remotely and on-site

- Utilizing available hardware and software to support the effective conduct of the clinical study data review and capture

- Verifying site compliance with electronic data capture requirements

- Managing site-level activities and communication to ensure project objectives, deliverables, and timelines are met

- Providing guidance at the site and project level towards audit readiness standards

- May act as primary liaison with study site personnel or in collaboration with Central Monitoring Associate

- Preparing for and attending Investigator Meetings and/or sponsor face-to-face meetings

- Participating in and may lead global clinical monitoring/project staff meetings

- May provide direct supervision, training, and/or mentorship to more junior level CRAs

The ideal candidate will have:

- Bachelor's degree or RN in a related field or equivalent combination of education, training, and experience

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

- Excellent communication, presentation, and interpersonal skills

- Ability to manage required travel of up to 75% on a regular basis

## Skills

### Required
- Good Clinical Practice
- ICH Guidelines
- clinical monitoring
- site management
- regulatory compliance

### Nice to have
- Oncology
- Spanish

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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/Site-Care-Partner--Sponsor-dedicated----Buenos-Aires-only---Min-6--years-of-previous-monitoring-experience--ideally-in-Oncology-_25112421?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)