# On-site Monitor

**Company**: Syneos Health
**Location**: AUT-Remote
**Work arrangement**: onsite
**Experience**: mid
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/AUT-Remote/Site-Management---CRA-for-Real-World---Late-Phase-studies----open-to-diverse-EMEA-countries---_25002767?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_f31ba944-7db

## Description

Syneos Health is seeking an On-site Monitor to join their Clinical Solutions team. The successful candidate will perform site management activities in compliance with Company and Sponsor Standard Operating Procedures (SOPs) and Work Instructions (WIs).

**Job Responsibilities**

- Perform site management activities in compliance with SOPs and WIs

- Assure compliance with local regulations and guidance

- Conduct site management activities as per agreed Scope of Work (SoW), Site Management Plan (SMP) and relevant guidelines

- Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness

- Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents

- Demonstrates diligence in protecting the confidentiality of each subject/patient

- Assigned sites data review, assisting with data query resolution and missing data follow-up

- Maintain effective, accurate and timely communication with site staff and project team

- Ensure all assigned sites are trained and compliant with requirements of the study protocol, informed consent process, data collection requirements/data collection tools and safety reporting

- Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions

**Qualifications**

- Minimum 1 year relevant onsite monitoring experience required

- BA/BS degree in science/health care field or nursing degree or equivalent combined education and experience

- Must be proficient in Microsoft Office Suite (Word, Excel, and PowerPoint), email/voicemail, and Clinical Trial Management and EDC systems

- Previous site management (in-house, on-site, Study Coordinator) or equivalent experience

- Excellent communication, time management, organizational, documentation and customer service skills

- Knowledge of local requirements for Real World Late Phase study designs as well as Real World Research and relevant regulations including GPP

- Excellent customer focus (internal and external) and able to interact professionally with a client organization and study site

- Willingness to work within a team-oriented environment

- Ability to handle multiple tasks (across multiple studies as necessary) and prioritize accordingly to achieve study timelines

- Excellent command of written and spoken local language, if not English, as well as English required

- Ability to develop good working relationships via oral communication and good phone etiquette

- Ability to travel up to 60% on a regular basis depending on assignments and study phase

**Additional Information**

Syneos Health is committed to building an inclusive culture – where you can authentically be yourself.

## Skills

### Required
- German
- Microsoft Office Suite
- Clinical Trial Management
- EDC systems
- Good Pharmacoepidemiology Practices (GPP)
- International Conference on Harmonization - Good Clinical Practice (ICH-GCP)

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/AUT-Remote/Site-Management---CRA-for-Real-World---Late-Phase-studies----open-to-diverse-EMEA-countries---_25002767?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)