# Site Activation Coordinator

**Company**: IQVIA
**Work arrangement**: remote
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Belgrade-Serbia/Regulatory-and-Start-Up-Specialist---Serbia_R1563175?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_d867b464-353

## Description

Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.

As a Home Based role requiring a RSU with contracts experience, you will:

- Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary

- Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines

- Perform start up and site activation activities according to applicable regulations, SOPs and work instructions

- Distribute completed documents to sites and internal project team members

- Prepare site regulatory documents, reviewing for completeness and accuracy

- Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information

- Review and provide feedback to management on site performance metrics

- Review, establish and agree on project planning and project timelines

- Ensure monitoring measures are in place and implement contingency plan as needed

- Inform team members of completion of regulatory and contractual documents for individual sites

- Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines

- Provide local expertise to SAMs and project team during initial and on-going project timeline planning

- Perform quality control of documents provided by sites

- May have direct contact with sponsors on specific initiatives

## Skills

### Required
- regulatory compliance
- site activation
- clinical research
- project management

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Belgrade-Serbia/Regulatory-and-Start-Up-Specialist---Serbia_R1563175?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)