Director / Manager of Clinical Operations-Onsite in Miami, FL

Job Description

Job Description

Location : This role is onsite at CPMI in Miami, FL

If you are not local to Miami, let's discuss how to get you there!

This is a newly created role at an amazing, top clinical research site located in Miami, FL

About Company : Who is ERG?

ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with an expertise in early and late-stage neuroscience drug development. With 19 wholly owned clinical sites and 5 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 340+ in-patient beds, a large and growing database of patients suffering from mental illness, neurological disorders, sleep disorders, addictions, Acute and Chronic Pain, diabetes and other illnesses as well as normal healthy volunteers who participate in trials for the advancement of medicine. With access to over 32 million patients / subjects and 5000 + completed trials, ERG continues to grow its capabilities and expand into indications where there are tremendous unmet medical needs in the United States and globally.

About the Role :

We are seeking a highly qualified Manager / Director of Clinical Operations, Phase I, to oversee clinical trials, ensuring protocol adherence, and managing both staff and operational aspects of studies. This role demands strict compliance with GCP, ICH guidelines, and company SOPs. Core duties include staff management, protocol review, quality assurance, and overall study supervision.

Responsibilities :

• Lead and mentor the clinical operations team to promote a collaborative and efficient environment.
• Ensure protocol compliance and maintain high-quality standards across studies.
• Collaborate closely with Principal Investigators and Site Directors to assign studies and develop enrollment strategies.
• Oversee human resources functions, including staff evaluations, recruitment, and training.
• Monitor adherence to protocols, reporting any deviations to sponsors and regulatory bodies.
• Coordinate with Site Director and Principal Investigator to assign primary clinical research coordinators.
• Review study components with Principal Investigators and Site Directors, identifying areas requiring clarification before study initiation.
• Conduct study closeout procedures.
• Perform additional duties as needed to adapt to the evolving needs of CPMI.
• Ensure compliance with all applicable regulations and guidelines, including FDA, ICH, and GCP

Minimum Qualifications :

Preferred Qualifications :

Benefits Overview :

Our comprehensive benefits package includes :