REGULATORY SPECIALIST - CRI

Methodist Health System; Dallas (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

The Regulatory Specialist position at Methodist Health System in Dallas, TX focuses on the regulatory components of clinical trials, including Phase II/IV trials, IITs, and retrospective data analysis. This role supports organization goals and ensures compliance with ICH-GCP guidelines.

You will coordinate IRB submissions, maintain essential regulatory documents, and facilitate the informed consent process while collaborating with study teams to protect patient safety and data integrity.

Qualifications

• Bachelor's degree in a related field required; Master’s preferred.
• Experience in clinical research and regulatory affairs required.
• GCP certification preferred; strong documentation skills.

Responsibilities

• Review clinical research protocols for regulatory requirements.
• Coordinate regulatory submissions and IRB approvals.
• Maintain regulatory documents per ICH-GCP standards.
• Support informed consent processes with study teams.
• Communicate with sponsors, investigators, and coordinators.
• Identify and report adverse events per FDA guidelines.

Skills

Regulatory affairs

Clinical research

GCP certification

IRB submissions

Documentation and record-keeping

Communication skills

Education

Bachelor's degree

Master’s degree preferred

Tools

Microsoft Office

Job description

## REGULATORY SPECIALIST - CRIApplylocations: Dallas, Texastime type: Full timeposted on: Posted Yesterdayjob requisition id: JR1000037333**Hours of Work :**8am-5pm**Days Of Week :**M-F**Work Shift :****Job Description :**Your Job: The Regulatory Specialist will perform expertise in the regulatory component of all clinical research trials to include, but not limited to; Phase II and IV clinical, investigator initiated trials (IITs), and retrospective analysis of clinical data. The Regulatory Specialist will support the mission, vision, values, and strategies of the Methodist Health System.Your Job Requirements:• Bachelor's degree required; Master’s degree preferred• CCRC or CCRP (preferred)• GCP certification (preferred)• 1 year of experience in a medical or clinical setting (required)• 1 year of experience in clinical research (required)• 1 year of experience in research regulatory affairs (required)• Strong proficiency using Microsoft Office products • Superior oral and written communication skills • Strong process orientation • Detail oriented, logical, and methodological approach to problem solving • Ability to provide vision and leadership. Your Job Responsibilities: • Communicate clearly and openly• Build relationships to promote a collaborative environment• Be accountable for your performance• Always look for ways to improve the patient experience• Take initiative for your professional growth• Be engaged and eager to build a winning team• Review clinical research protocols to determine logistical components of regulatory requirements• Obtain and facilitate tracking of relevant regulatory documents for clinical trials submission and management.• Maintain appropriate communications between sponsors, investigators, other research team members for clinical trials assigned.• Assist in the development of clinical trial documents for signature of principal investigator and approval by the IRB.• Create and/or adapt clinical trial informed consent documents for Institutional Review Board (IRB) submission.• Maintain regulatory documents in accordance with International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) guidelines.• Attend study specific training, investigator meetings as assigned, and MHS required training.• Facilitate informed consent process for principal and sub-investigators.• Assist clinical research coordinators in the identification and reporting of appropriate adverse events in accordance with Food and Drug Administration, sponsor protocol, and IRB regulations and guidelines.• Prepare and submit amendments to protocols and informed consent documents as required.Methodist Health System is a faith-based organization with a mission to improve and save lives through compassionate, quality healthcare. For nearly a century, Dallas-based Methodist Health System has been a trusted choice for health and wellness. Named one of the fastest-growing health systems in America by *Modern Healthcare*, Methodist has a network of 12 hospitals (through ownership and affiliation) with nationally recognized medical services, such as a Level I Trauma Center, multi-organ transplantation, Level III Neonatal Intensive Care, neurosurgery, robotic surgical programs, oncology, gastroenterology, and orthopedics, among others. Methodist has more than two dozen clinics located throughout the region, renowned teaching programs, innovative research, and a strong commitment to the community. Our reputation as an award-winning employer shows in the distinctions we’ve earned:* Great Place to Work Certified 2026-2027* Glassdoor’s Best Places to Work 2025 & 2026* Glassdoor’s Best Places to Work in Healthcare, Biotech & Pharma 2026* TIME’s Best Companies for Future Leaders 2025 & 2026* Newsweek’s America’s Most Admired Workplaces 2026* Glassdoor’s Best-Led Companies 2025* Fortune Best Workplaces in Health Care 2025* Military Friendly Gold Employer 2025* Becker’s Hospital Review 150 Top Places to Work in Healthcare 2025* Newsweek’s Americas Greatest Workplaces 2025