Trial Runners is an ophthalmology CRO providing biotech and pharmaceutical companies with clinical research management services. They are also a company that has a reputation for solid clinical trial management execution.
|Headquarters|| 116 W. Villard
Dickinson, ND 58601 USA
|Key people|| PATRICK HEALY, MPH
JILL HEALY President & CEO
Trial Runners, LLC was launched in 2006 by founders Patrick Healy and Jill Healy. Together they bring over 35 years of clinical research management experience from within pharmaceutical companies. Knowing the challenges biotech and pharmaceutical companies face, they saw an opportunity to improve upon the ophthalmology clinical Contract Research Organization (CRO) Industry.
Their background and insight inspired them to enhance clinical research management through innovative solutions. Out of experience grew a philosophy focused on responsiveness, execution, expert project management, lower costs and valued relationships. Providing you with experienced clinical professionals means accurate, timely research aligned with your budget.
Headquarters for Trial Runners is located in North Dakota. Jill was born and raised in North Dakota and after making many trips from New York City with Patrick to North Dakota to visit family, the founders fell in love with the state and realized the incredible opportunity that existed to launch a top tier ophthalmology CRO in the state. In 2014, Forbes magazine ranked North Dakota the #2 best state in the nation for business. In 2013, Livability.com ranked Dickinson, ND the #1 best small town in America. 
•Clinical Development and Strategy Consulting
•Safety and Pharmacovigilance
The TR Way
Clinical projects involve a myriad of details to consider, and without a clear plan it is easy to get bogged down in the details and lose track of what is important.
SAFETY AND PHARMACOVIGILANCE
Trial Runners offers global safety and pharmacovigilance services to assist in all phases of clinical research. The team provides experience, consistency and dedicated medical and safety staff with services that include:
- Development and utilization of a Serious Adverse Event (SAE) and medical management plan (SMMP)
- Processing of SAEs including medical review
- Preparation, writing, and distribution of SAE narratives and safety reports (MedWatch, CIOMS) including submission to regulatory authorities
- AE and SAE reconciliation of safety and clinical databases
- Medical and safety coverage available 24 hours, 7 days a week
- Safety Quality Assurance – ongoing review of safety data including monitoring and identifying safety trends
- Safety training and education
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