Clinical Research Associate, Single Sponsor
IQVIA
full-time
Posted on:
Location Type: Office
Location: Warsaw • Poland
Visit company websiteExplore more
Salary
💰 PLN 132,800 - PLN 280,000 per year
About the role
- Perform monitoring and site management work to ensure that sites are conducting the study(ies)
- Responsibilities include site selection, initiation, monitoring and close-out visits
- Supporting the development of a subject recruitment plan
- Establishing regular lines of communication and administering protocol training to assigned sites
- Evaluating the quality and integrity of site practices
- Managing progress by tracking regulatory submissions and data query resolution
Requirements
- Bachelor's degree in a health care or other scientific discipline or educational equivalent
- Experience in on-site monitoring of clinical trials
- Written and verbal communication skills including good command of Polish and English language
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
site managementsite selectionmonitoringprotocol trainingregulatory submissionsdata query resolutionclinical trials
Soft skills
written communicationverbal communicationinterpersonal skills