MedTech Site Manager 1
IQVIA · Washington, DC
Clinical OperationsFull-time$75k–$124kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA MedTech seeks a clinical research professional to manage investigator sites and monitoring activities for medical device and diagnostics trials. The role supports clinical affairs operations in compliance with GCP guidelines and regulatory standards, reporting to the Director of Clinical Affairs.
What they're looking for
- Bachelor's degree in pharmacy, pharmaceutics, or related scientific field
- 2+ years clinical trial experience; monitoring experience preferred
- Comprehensive knowledge of GCP guidelines and clinical monitoring procedures
- Experience with Electronic Data Capture (EDC) and trial management systems
- Strong written and verbal communication and presentation abilities
- Proficiency in MS Office, Excel, Word, and PowerPoint
- Strong analytical, critical-thinking, and problem-solving skills
What you'll be doing
- Review and approve regulatory documents for clinical trial implementation and monitoring
- Ensure monitoring activities align with company SOPs and Clinical Monitoring Plans
- Assist with site recruitment, training, audits, and quality management activities
- Maintain accuracy and completeness of Trial Master File throughout project lifecycle
- Develop and maintain relationships with clients, team members, and site personnel
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.