Sheridan Clinical Research, Inc. ("Sheridan Clinical Research"), and its research affiliate, is a comprehensive full service clinical research division of one of the nation's largest physician practice management organizations. The physician practice management organization employs over 800 physicians and allied healthcare providers and provides a team of Regulatory, Patient Recruitment, Compliance, Marketing, and Quality Assurance Specialists. 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, General Surgery, Colorectal Surgery, Breast Surgery, Maternal, Fetal Medicine

"Our Expertise is your Advantage"

Dedicated full-time and part-time research sites within premiere office-based private group practices.

Additionally, hospital-based Anesthesia, Pain Management, Neonatology and Emergency Medicine services are provided at facilities in Florida, Texas, Louisiana, New Mexico, North Carolina, Pennsylvania, Arizona, Connecticut, Colorado, Arkansas, Virginia, Maryland and Missouri with full research capabilities.

Sheridan Clinical Research Site Capabilities include:

• Centrifuge
• Dedicated Monitor Workspace
• Dedicated Internet
• Electronic CRF capabilities
• Electronic Diary Capabilities
• Double Locked Drug Storage
• Dedicated Refrigerator
• Freezer
• Blood Draw Stations
• Full Service Laboratory
• Coordinators with Private Offices

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 60 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
• Integrity of Clinical and Data Management
• Proven Reputation with Established Sponsor Relationships
• Strategic Recruitment Plan for Each Protocol
• Ambitious Enrollment Efforts
• Nation-Wide Research Capabilities
• Prompt Regulatory Submissions
• Positive Business Demeanor with Local and Central IRBs
• Continuing Staff Education
• Proactive and Responsive Management Team

Electronic Patient Database, Number of Patient Encounters Company wide >1 million annually, Diverse National Representative of Patient Populous Types of Patients Seen in the Following Areas:

• Anesthesia
• Pain Management
• Surgery General & Colorectal
• Women's Health
• Obstetrics
• Neonatology
• Gynecological Oncology
• Emergency Medicine and 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 data, and we abide by all applicable laws, regulations and guidelines governing patient confidentiality.
• 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).
• 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.

• A subject friendly environment.
• Protocol-specific tracking systems
• Stringent Investigator involvement
• Capabilities to work with Central and Local IRBs

For more information, please contact:

Deena Bernstein
Director of Clinical Research
Sheridan Clinical Research, Inc.
1613 N Harrison Parkway
Bldg. C
Sunrise, FL 33323 USA
Phone: (954) 838-2729
Fax: (954) 851-1715
E-mail:

If you are interested in contacting this center to discuss placing a clinical trial there, please complete and send the E-mail form below. A representative from the research center will then follow up with you.

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Last updated on February 19, 2008

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