If you are interested in learning more about collaborating with RxTrials please call 410-465-2455 or send an email to us at info@rxtrialsinc.com.

RxTrials is a multi-specialty clinical research organization that has assembled a large network of physicians and hospitals in Maryland, Washington D.C., and Virginia. RxTrials collaborates with physicians and hospitals interested in conducting clinical trials with pharmaceutical and device companies. RxTrials provides the clinical trials and minimizes physicians' work burden by providing the staff and expertise necessary to implement the trial more successfully. RxTrials is only paid more for patients enrolled and work completed.

What Rx Trials provides the physician:

• Attendance at Investigator Meeting.
• Inservice for staff.
• Active screening of potential study subjects.
• Implementation of the study.
• Provision of Quality Assurance.
• Appropriate clinical trials for your consideration.
• Preparations for pre-site visit with sponsor.
• Budget and contract negotiation.
• IRB preparation and submission.
• Development of necessary research documents.
• Development of recruitment strategies.
• Implementation of the study, coordination of all visits, and oversight of all tests and procedures
• Complete case report forms.
• Monthly meetings and close out with sponsor.

All Investigators and research staff receive ongoing human subject protection education.

RxTrials carefully evaluates each research study to ensure success for the sponsor.

RxTrials sites consistently exceed enrollment goals and generate quality data.

Our Subject Recruitment Specialist recruits study participants through proactive primary investigator involvement, intuitive marketing, and public relations strategies.

Experienced clinical research professionals expedite contract negotiations, budget development, accounting, human resources, and overall study administration.

On-site research coordinators guarantee prompt study initiation, effective interactions with study subjects and the research team, and ensure compliance with all human subject protection regulations. Providing individual attention to the needs of each sponsor and clinical trial is our priority.

The diverse metropolitan population, exceeding 5 million, allows for compliance with FDA standards for ethically and racially diverse enrollment.

Ongoing outreach and public education at community events heightens awareness of the clinical trial process and opportunities for subject participation, which eventually leads to successful enrollment and retention.