# Site Activation Specialist

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

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Buenos-Aires-Argentina/Site-Activation-Specialist_R1573057?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_9b3c5017-f4d

## Description

We are seeking a Site Activation Specialist to work full-time from home in Argentina.

As a Site Activation Specialist, you will 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. May also include maintenance activities.

**Essential Functions**

- 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.

- 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.

- Establish and agree on project planning and project timelines.

- 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.

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

- Perform quality control of documents provided by sites.

**Qualifications**

- Bachelor's degree

- 2+ years of clinical research experience, clinical trial assistant experience is a plus.

- Experience in clinical research regulatory activities in Argentina, including presentations to ethics committees and ANMAT (SSU and maintenance phases)

- Good command of English Language

- Excellent communication and interpersonal skills

- Excellent organization and prioritization skills

## Skills

### Required
- clinical research
- regulatory activities
- English Language

### Nice to have
- clinical trial assistant
- presentations to ethics committees
- ANMAT

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Buenos-Aires-Argentina/Site-Activation-Specialist_R1573057?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)