Global Clinical Research Manager – Orthopedic Devices

Medartis; Miami (FL); On-site; USD 90,000 - 130,000; Full time

Job summary

Medartis seeks a clinical studies professional to manage the portfolio of clinical research projects and sites, ensuring compliance with FDA/GCP and regulatory standards. The role requires coordinating with investigators, CROs, and internal teams, and travel up to 20% to study sites and conferences.

The successful candidate will lead data collection, protocol development, and regulatory submissions while maintaining high-quality study documentation and education for site staff.

Qualifications

• Degree in a STEM field at a university level or equivalent professional experience/training.
• PhD and GCP certificate desirable.

Responsibilities

• Cultivate a portfolio of clinical research projects and a network of sites/investigators to support Medartis regulatory needs.
• Create and maintain customer contacts for visits, trainings and advisory roles as the liaison between internal and external partners.
• Develop and maintain quality system processes to ensure compliance with regulatory and legal requirements.
• Select and support preclinical and clinical studies, including patient registries and PMA considerations.

Skills

Willingness to travel

Fluent English

Communication skills

Office proficiency

Education

STEM degree

PhD desirable

Tools

EDC software

Job description

Medartis seeks a clinical studies professional to manage the portfolio of clinical research projects and sites, ensuring compliance with FDA/GCP and regulatory standards. The role requires coordinating with investigators, CROs, and internal teams, and travel up to 20% to study sites and conferences.

The successful candidate will lead data collection, protocol development, and regulatory submissions while maintaining high-quality study documentation and education for site staff.