MedTech Site Manager 1 (MedTech)

Location: Washington, DC, United States of America

Salary: $74,500–$124,100 annualized base pay

Company

IQVIA MedTech and MCRA provide clinical research, regulatory, market access, and post-market solutions for the medical device and diagnostics industry.

What you will do

• Manage investigator site and CRA activities for assigned clinical studies.
• Review and approve regulatory documents and clinical protocols supporting trial implementation, monitoring, evaluation, and regulatory submissions.
• Ensure remote and on-site monitoring activities follow SOPs and Clinical Monitoring Plans.
• Support clinical study planning, investigator and site recruitment, site training, audits, and quality management.
• Maintain accurate and complete Trial Master Files throughout the study lifecycle.
• Build effective relationships with clients, project teams, investigators, study coordinators, and other site personnel.

Requirements

• Bachelor’s degree in pharmacy, pharmaceutics, or a related scientific discipline.
• At least 2 years of clinical trial experience; monitoring experience is preferred.
• Comprehensive knowledge of and fluency in Good Clinical Practice and clinical monitoring procedures.
• Understanding of the therapeutic area assigned to clinical projects.
• Experience with Electronic Data Capture systems and clinical trial management systems.
• Strong written, verbal, presentation, research, analytical, critical-thinking, and problem-solving skills, plus proficiency with MS Office, Excel, Word, and PowerPoint.

Nice to have

• Clinical monitoring experience.
• EndNote experience.

Culture & Benefits

• Full-time employment with health, welfare, and other benefits.
• Potential incentive plans, bonuses, and additional compensation may be available depending on the position.
• Work is conducted in accordance with GCP guidelines, company and client SOPs, and applicable FDA and regulatory requirements.