Clinical Trials Regulatory Officer – Maintenance Associate
IQVIA
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇸🇰 Slovakia
Visit company websiteJob Level
JuniorMid-Level
About the role
- Support study delivery during the maintenance phase of the study
- Work alongside MLs and CTRMs to complete all necessary maintenance and regulatory activities
- Manage and utilize study dashboards
- Analyze data and monitor study metrics and compliance
- Prepare project status reports and presentation materials for internal project team and customer meetings
- Connect with key internal stakeholders for the project
Requirements
- Good knowledge of clinical research domain and applicable regulatory requirements/ guidelines
- Good knowledge of Clinical Systems (CTMS, TMF, Workflows etc)
- Expert with MS Excel and good knowledge of MS Office applications and Spotfire reports
- Strong Analytical skills
- Ability to work on multiple projects/tasks balancing competing priorities
Benefits
- Training and Mentorship: Commitment to professional growth
- Ongoing support and development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
data analysisstudy metrics monitoringproject status reportingregulatory complianceclinical research knowledgeCTMSTMFSpotfireMS ExcelMS Office
Soft skills
analytical skillsproject managementcommunicationstakeholder engagementprioritizationteam collaboration