# Site Activation Coordinator

**Company**: IQVIA
**Experience**: senior
**Salary**: zł151,200.00 - zł280,700.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Warsaw-Poland/Reg---Start-Up-Spec-2_R1573302?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_5ca9cca1-13f

## 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. 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.

- 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.

- May have direct contact with sponsors on specific initiatives.

Qualifications:

- Bachelor's Degree in life sciences or a related field and 3 years' clinical research or other relevant experience.

- 3 years clinical research experience, including 1 year experience in a leadership capacity.

- In-depth knowledge of clinical systems, procedures, and corporate standards.

- Good negotiating and communication skills.

- Effective communication, organizational, and interpersonal skills.

- Ability to work independently and to effectively prioritize tasks.

- Ability to manage multiple projects.

- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.

- Understanding of regulated clinical trial environment and knowledge of drug development process.

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

## Skills

### Required
- clinical research
- regulatory guidelines
- GCP/ICH
- communication skills
- organizational skills
- interpersonal skills
- leadership

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Warsaw-Poland/Reg---Start-Up-Spec-2_R1573302?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)