Clinical Monitoring Manager - SEALit Neurodevice Trial

Job Description

Location: Hybrid (Preferred: Northwest Ohio or Southern Ohio Metropolitan Area; Open to Nationwide Applicants)

Reports to: Chief Medical Officer

Salary: $80,000 – $98,000 (commensurate with experience; higher range available for top-tier candidates)

Job Type: Full-time, Hybrid

About MedX CRO

MedX CRO is a leading U.S.-based contract research organization specializing in innovative clinical trials for medical devices and therapies. We are currently managing the SEALit neurodevice clinical trial—a breakthrough in neurological care—with sites across the U.S. and internationally. Our mission is to advance patient outcomes through rigorous, ethical, and compliant research.

Position Overview

We are seeking a Clinical Monitoring Manager to serve as the primary medical expert for the SEALit neurodevice clinical trial. This hands-on role ensures participant safety, regulatory compliance, and operational excellence. Ideal candidates are detail-oriented, collaborative, and passionate about advancing neurodevice innovation.

Key Responsibilities

Serve as the primary medical point of contact for the SEALit neurodevice clinical trial

Oversee clinical trial activities including adverse event reporting, protocol adherence, and data review

Collaborate with cross-functional teams to ensure compliance with FDA and ICH-GCP guidelines

Provide medical input on protocol development, study design, and data analysis

Lead safety review meetings and contribute to clinical study reports

Mentor clinical staff and foster a culture of excellence and continuous improvement

Ensure adherence to regulatory requirements and company SOPs

Participate in investigator meetings and site trainings as needed

Qualifications

Medical degree (MD, DO, or equivalent) required

Minimum 3 years’ experience in clinical trial medical monitoring (medical device focus preferred)

Proven experience in FDA-regulated trials

Strong knowledge of FDA regulations, ICH-GCP, and clinical trial processes

Excellent leadership, communication, and analytical skills

Commitment to ethical standards and professional integrity

Supervisory Responsibilities

Oversight of clinical trial staff and site medical personnel (as assigned)

Why Join Us?

Make a meaningful impact in a high-growth, innovative company

Collaborate with leading physicians, scientists, and engineers in the neurodevice field

Opportunity for expanded responsibilities and career growth

MedX CRO is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Full-time

Hybrid remote