# 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/Sydney-North-New-South-Wales-Australia/Senior---Clinical-Research-Associate_R1525252?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_0deaf7a0-dc2

## Description

We are seeking a Clinical Research Site Manager to perform monitoring and site management work, ensuring sites conduct studies and report data according to study protocols, regulations, and sponsor requirements.

**Essential Functions:**

- Conduct site monitoring visits, including selection, initiation, monitoring, and close-out visits, following contracted scope of work and regulatory requirements

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

- Provide protocol and related study training to assigned sites, establishing regular communication lines to manage project expectations and issues

- Evaluate study site practices, escalating quality issues as needed

- Manage study progress, tracking regulatory submissions, recruitment, case report form completion, and data query resolution

- Ensure site documents are available for filing in the Trial Master File and verify Investigator's Site File maintenance

- 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

- At least 1 year of on-site monitoring experience

- Equivalent combinations of education, training, and experience may be accepted

- Good knowledge of clinical research regulatory requirements, including Good Clinical Practice and International Conference on Harmonization guidelines

- Therapeutic and protocol knowledge, provided through company training

- Computer skills, including Microsoft Word, Excel, and PowerPoint, and proficiency in using laptops and mobile devices

- Strong written and verbal communication skills, with good command of English

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

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

## Skills

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

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Sydney-North-New-South-Wales-Australia/Senior---Clinical-Research-Associate_R1525252?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)