Regulatory Coordinator

Headlands Research, Inc.; Lake Worth (TX); On-site; USD 60,000 - 85,000; Full time

Job summary

Headlands Research is seeking a full-time Regulatory Coordinator for their clinical trial sites. The role involves managing regulatory processes, ensuring compliance, and serving as a primary contact for clinical studies. Ideal candidates have 3+ years in clinical trials, strong project management skills, and a detail-oriented approach. Join a leading company aiming to advance participant engagement within clinical research.

Qualifications

• 3+ years experience in clinical trials as a regulatory person or clinical coordinator required.
• Knowledge of regulatory policies/study start-up/maintenance.
• Experience with clinical trial processes and contract management.

Responsibilities

• Set up and maintain checklists, dashboards, reports, and document templates for new projects.
• Perform quality control reviews of essential site regulatory documents.
• Serve as the primary point of contact for all clinical studies from a regulatory perspective.

Skills

Project Management

Communication

Organizational Skills

Critical Thinking

Detail-oriented

Multitasking

Interpersonal Skills

Customer Service

Job description

Overview

At Headlands Research, we are building a best in class clinical trial network. We’re an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant engagement Founded in 2018, our company operates 20+ clinical trial sites in the US and Canada with rapid plans for expansion.

This role is located onsite in Atlantis, FL and is a full time position. You can learn more about us at www.headlandsresearch.com.

The Role

JEM Research Institute, a Headlands Research site, is looking for a Regulatory Coordinator. The Regulatory Specialist manages and executes the site identification process and performs regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements. They prepare and manage site regulatory documentation, reviews and negotiate site regulatory documents with CROs and sponsors, maintain, review, and report on site performance metrics, serve as the primary point of contact for investigative sites, track completion of regulatory documents and establish project timelines. They work with Quality Assurance department to ensure training and regulatory documents are FDA ready at all times.

Responsibilities

• Set up and maintain checklists, dashboards, reports, and document templates for new projects.
• Perform quality control reviews of essential site regulatory documents.
• Serve as the primary point of contact for all clinical studies from a regulatory perspective.
• Prepare and maintain regulatory documents from study start up to study end.
• Work with study staff (coordinators/recruiters/investigators) to ensure training and documents are in compliance and FDA ready.
• Maintain compliance with all company policies and procedures

Qualifications

• 3+ years experience in clinical trials as a regulatory person or a clinical coordinator required
• Knowledge of regulatory policies/study start-up/maintenance
• Experience with study startups, clinical trial processes
• Experience with contract management
• Excellent project management skills
• Excellent organizational and time management skills
• Excellent oral communication skills
• Detail-oriented
• Strong critical thinking skills
• Strong ability to multitask
• Strong computer skills; CRIO or electronic source experience a plus
• Ability to communicate clearly and effectively (written and oral)
• Excellent interpersonal and customer service skills
• GCP/Regulatory knowledge