# Clinical Research Site Manager

**Company**: IQVIA
**Experience**: mid
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Illkirch-Graffenstaden-France/CRA2--Freelancer-_R1345974?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_90c452d1-64b

## Description

We are seeking a Clinical Research Site Manager to perform monitoring and site management work, ensuring sites conduct studies and report study data as required by the study protocol, regulations, and sponsor requirements.

Responsibilities:

- Conduct site monitoring visits in accordance with contracted scope of work and regulatory requirements

- Collaborate with sites to adapt, drive, and track subject recruitment plans

- Provide protocol and related study training to assigned sites and establish regular communication lines

- Evaluate study site practices and escalate quality issues as needed

- Manage study progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution

- Maintain site documents and verify Investigator's Site File in accordance with GCP and local regulatory requirements

- Create and maintain documentation regarding site management, monitoring visit findings, and action plans

- Collaborate with study team members for project execution support

Qualifications:

- Bachelor's degree in a scientific discipline or healthcare preferred

- At least 1 year of on-site monitoring experience

- Knowledge of applicable clinical research regulatory requirements (GCP and ICH guidelines)

- Good therapeutic and protocol knowledge

- Proficiency in Microsoft Word, Excel, and PowerPoint, and use of a laptop computer and iPhone and iPad

- Excellent written and verbal communication skills, including good command of English

- Organizational, problem-solving, and time and financial management skills

- Ability to establish and maintain effective working relationships with coworkers, managers, and clients

## Skills

### Required
- Good Clinical Practice (GCP)
- International Conference on Harmonization (ICH) guidelines
- Microsoft Word
- Excel
- PowerPoint
- English

### Nice to have
- scientific discipline
- healthcare
- clinical research regulatory requirements

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Illkirch-Graffenstaden-France/CRA2--Freelancer-_R1345974?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)