Client-Facing MedTech Clinical Safety Lead

5PY IQVIA RDS Inc.; Washington (District of Columbia); On-site; USD 86,000 - 215,000; Full time

Job summary

IQVIA Inc. seeks a MedTech Clinical Safety Manager to coordinate safety projects across clinical and post-market programs. You will manage day-to-day execution, timelines, safety reviews, documentation, and client communications under senior leadership guidance.

The role requires 4+ years in clinical research or medical device safety, strong organizational skills, and proficiency with MS Office. You will collaborate with cross-functional teams to meet contractual commitments and ensure

Qualifications

• Bachelor's degree in Nursing, Life Sciences, Health Sciences, Public Health, Biology, Biomedical Sciences, or related field.
• 4+ years of experience in clinical research, medical device safety, project coordination or management, healthcare, quality, regulatory affairs, or related field.
• Experience supporting CECs, DSMBs, or other independent safety review committees.
• Experience coordinating client-facing projects, timelines, deliverables, meetings, and operational activities across multiple stakeholders.
• Strong organizational and prioritization skills with ability to manage multiple assignments and deadlines.
• Excellent verbal and written communication skills with ability to present information clearly to internal and external stakeholders.
• Proficiency with Microsoft Office applications including Excel, Word, PowerPoint, and Outlook.
• Ability to work independently and in a fast-paced, collaborative team.

Responsibilities

• Manage day-to-day execution of assigned client safety projects across medical device clinical studies and post-market safety activities, with oversight from senior Clinical Safety leadership.
• Develop and maintain project plans, timelines, deliverables, documentation requirements, meeting schedules, and action-item trackers for assigned safety projects and committee activities.
• Proactively elevate risks, scope changes, resource needs, or potential delays.
• Lead and coordinate Clinical Events Committee (CEC) and Data Safety Monitoring Board (DSMB) meetings, including scheduling and distributing materials, coordinating stakeholders, and tracking action items.
• Collect, review, organize, and maintain safety documentation including adverse event reports, product complaints, and safety logs.
• Prepare and maintain project status reports, utilization and delivery metrics, and client-facing materials.
• Serve as day-to-day contact for project activities and support resolution of delivery issues under guidance of senior staff.
• Collaborate with Clinical Operations, Regulatory Affairs, Quality, Medical Affairs, and finance to coordinate resources and ensure delivery commitments.

Skills

Project coordination

Client-facing

Regulatory knowledge

Communication skills

MS Office

Education

Bachelor's degree

Tools

CTMS

eTMF systems

Job description

IQVIA Inc. seeks a MedTech Clinical Safety Manager to coordinate safety projects across clinical and post-market programs. You will manage day-to-day execution, timelines, safety reviews, documentation, and client communications under senior leadership guidance.

The role requires 4+ years in clinical research or medical device safety, strong organizational skills, and proficiency with MS Office. You will collaborate with cross-functional teams to meet contractual commitments and ensure