Clinical Site Lead

Job Duties

• Maintains clinical study site maintenance, data and source documentation collection.
• Field monitors clinical trials, ensuring compliance with study protocols and regulations.
• Ensures completeness and accuracy of data, reporting adverse events and protocol deviations.
• Coordinates initiation of clinical sites with assigned Field Clinical Engineer or designer and in-house personnel.
• Collaborates with study teams to enroll sites, facilitate enrollment of study subjects, and resolve data queries.
• Promptly reports findings of monitoring visits according to SJM processes.
• Collaborates with in-house teams to ensure complete submission of study documents.
• Trains site personnel and mentors less experienced clinical team members.

Requirements

• Bachelor’s degree from an accredited university or college, preferably in natural science, pre-medicine, nursing, bioengineering, or a related field.
• 10 years of experience in clinical research monitoring.
• Ability to interpret basic clinical data and meet deadlines.
• Effective communication skills with internal and external customers.

Preferred Qualifications

• Previous related experience in a medical device/pharmaceutical company or clinical experience in a hospital environment.
• A general familiarity with cardiac, vascular, and/or neuromodulation technologies.
• Certification by an industry-recognized professional society (e.g., SoCRA or ACRP).