Research Center Profile:
Sheridan Clinical Research, Inc.
Infections and Infectious Diseases
Obstetrics/Gynecology (Women’s Health)
Trauma (Emergency, Injury, Surgery)
"Our Expertise is your Advantage" We have dedicated full-time and part-time research sites within premiere office-based private group practices, community based hospitals, and outpatient surgical centers.
Our experienced clinical research team has worked in the following therapeutic areas:
Anesthesia, Neonatology, Gynecologic Oncology, Emergency Medicine, Obstetrics & Gynecology, Pain Management, Internal Medicine, and Maternal & Fetal Medicine.
Service lines include our hospital-based Anesthesia, Pain Management, Neonatology, Emergency Medicine, and Radiology services that are provided at facilities in Arkansas, Colorado, Connecticut, Florida, Georgia, Louisiana, Maryland, Massachusetts, Missouri, Nevada, New Jersey, New Mexico, North Carolina, Pennsylvania, Texas, Vermont, Virginia, Washington, and West Virginia with full research capabilities.
Dedicated Monitor Workspace
Electronic CRF Capabilities
Electronic Diary Capabilities
Double Locked Drug Storage
Blood Draw Stations
Full Service Laboratory
Coordinators with Private Offices
Sheridan Clinical Research, Inc. ("Sheridan Clinical Research"), and its research affiliate, is a multi-site, full-service clinical research company, part of one of the nation's largest physician practice management organizations. The physician practice management organization employs over 1,600 physicians and allied healthcare providers and provides a comprehensive management team of Director, Clinical Leader Investigators, Regulatory Specialists, Project Managers, Research Coordinators, Patient Recruitment, Compliance, Marketing, and Quality Assurance Experts. The Sheridan Clinical Research division conducts clinical trials in a wide range of specialty areas as described below.
Our experienced clinical research team has worked in the following therapeutic areas: Anesthesia, Neonatology, Gynecologic Oncology, Pain Management, Obstetrics / Gynecology, Emergency Medicine, Internal Medicine, Maternal, and Fetal Medicine.
Our Principal Investigators are Board Certified in their
specialty areas and all Investigators are required to complete
GCP/Research Compliance Training programs.
Investigators at Sheridan Clinical Research have successfully
completed over 140 pharmaceutical sponsored research protocols Phase
II-IV, since 2000.
Our Expertise is Your Advantage
10 years+ of Clinical Research Experience
Team of Certified Clinical Research Coordinators
Compliance and Quality Assurance Support Services
Internal Unique Feasibility Assessments
Site Mobilization Team for Streamlined Site Activation
Absolute Integrity of Clinical and Data Management
Proven Reputation with Established Sponsor Relationships
Strategic Recruitment Plan Constructed for Each Protocol
Ambitious Enrollment Efforts
Nation-Wide Research Site Capabilities in over 60 facilities
Expeditious Regulatory Submissions
Established Rapport with Local and Central IRBs
Electronic Data Capture Experience
Continuing Staff Education
Proactive and Responsive Management Team
Strategic Alliances with CRO’s and Sponsors
Electronic Patient Database, Number of Patient Encounters
Company wide >1 million annually, Diverse National
Representative of Patient Populous Types of Patients Seen in the
Maternal Fetal Medicine
Our Practiced Values:
Sheridan Clinical Research conducts clinical trials with integrity and we are committed to advancing human protection in research. We produce qualitative clean data, and we abide by all applicable laws, regulations and guidelines governing patient confidentiality and their welfare.
Each Sheridan Clinical Research site is attentive and respectful to subjects and their families as they progress through clinical trials and their treatment process.
Sheridan Clinical Research is dedicated and committed to not just meeting, but exceeding, the needs and goals of pharmaceutical sponsors and subjects.
We provide proactive and responsive leadership to the site's research staff (Principal Investigators and clinical research coordinators) and sponsor needs.
Sheridan Clinical Research requires that its clinical management team, consisting of physicians and clinical research professionals, is easily accessible and devotedly service-driven.
Sheridan Clinical Research requires its Principal Investigators and study coordinators to participate in clinical research educational training and programs on an ongoing basis; not only to maintain proficiency on the fundamentals of clinical research, but to become informed of the latest advancements in the industry. Distinguishing Factors
Sheridan Clinical Research maintains:
A subject friendly environment.
Protocol-specific recruitment plans
Monthly enrollment target measures
Accountable Investigator involvement
Capabilities of working with Central and Local IRBs
Sheridan Clinical Research, Inc. is a
Circle of Supporter member.
If you are interested in contacting this center to discuss placing a clinical
trial there, please complete and send the email form below. A representative from
the research center will then follow up with you.