MedTech Safety Project Lead

Job Summary

The MedTech Safety Project Lead provides operational project coordination and administrative support to the Clinical Safety team in the management of medical device and combination product safety activities across clinical and post-market programs. This role serves as a key coordinator of safety operations and independent safety review committees ensuring accurate tracking documentation and communication of safety information while supporting project execution regulatory compliance and cross-functional collaboration.

Job Responsibilities

• Provide day-to-day operational and administrative support to the Clinical Safety team across medical device clinical studies and post-market safety activities.

• Serve as the primary operational coordinator for assigned safety projects and committee activities ensuring deliverables timelines and documentation requirements are successfully executed.

• Assist with management of independent safety review committees (Clinical Events Committees (CECs) and Data Safety Monitoring Boards (DSMBs)) including preparation of meeting materials meeting participation and appropriate documentation of meeting outcomes.

• Coordinate safety-related project tracking timelines documentation meeting scheduling and action item follow-up.
• Support the collection review and maintenance of safety documentation including adverse event reports product complaints and safety tracking logs.

• Assist with case intake data entry quality checks and organization of safety records in accordance with internal procedures and regulatory requirements.
• Prepare meeting materials project status reports metrics and presentations for internal and client-facing discussions.

• Participate in client meetings and support preparation of client-facing safety updates reports metrics and presentations.

• Partner with Clinical Operations Regulatory Affairs Quality Medical Affairs and project teams to ensure timely communication and resolution of safety-related activities.
• Support inspection and audit readiness activities through maintenance of accurate documentation and safety records.
• Assist with implementation and refinement of safety processes workflows and standard operating procedures.
• Participate in safety team meetings and contribute to process improvement initiatives designed to enhance operational efficiency and compliance.
• Maintain awareness of applicable FDA EU MDR ISO 14155 vigilance and post-market surveillance requirements governing medical device safety activities.
• Perform other duties as assigned.

Job Qualifications

Required Qualifications

• Bachelors degree in Nursing Life Sciences Health Sciences Public Health Biology Biomedical Sciences or a related field.
• Minimum 2 years of clinical healthcare clinical research medical device or patient care experience.
• Strong organizational skills with the ability to manage multiple priorities and deadlines.
• Excellent verbal and written communication skills.
• Proficiency with Microsoft Office applications including Excel Word PowerPoint and Outlook.
• Demonstrated attention to detail and ability to maintain accurate documentation.
• Ability to work effectively in a fast-paced collaborative environment.

• Ability to participate in occasional early morning or evening meetings to support global teams and safety review committees. Flexible scheduling may be utilized to accommodate these requirements.

Preferred Qualifications

• Experience supporting medical device clinical trials clinical research safety quality regulatory affairs or complaint handling activities.

• Familiarity with safety databases clinical trial management systems (CTMS) electronic Trial Master Files (eTMF) or medical device complaint handling systems.

• Familiarity with adverse event reporting medical device vigilance post-market surveillance or product complaint processes.
• Understanding of Good Clinical Practice (GCP) FDA medical device regulations ISO standards or MDR requirements.
• Experience coordinating projects meetings or operational activities across multiple stakeholders.

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role when annualized is $51800.00 - $129600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge skills education and experience; location; and/or schedule (full or part-time). Dependent on the position offered incentive plans bonuses and/or other forms of compensation may be offered in addition to a range of health and welfare and/or other benefits.

Required Experience:

Senior IC