• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • COVID-19 Patient Resource Center
    • Clinical Trial Listings
    • What is Clinical Research?
    • Volunteering for a Clinical Trial
    • Understanding Informed Consent
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Market Research
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • White Papers
    • SOPs
    • eCFR and Guidances
  • White Papers
  • Clinical Trial Listings
  • Advertise
  • COVID-19
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Accurate Clinical Research Adds Second Location

Accurate Clinical Research Adds Second Location

January 25, 2010
CenterWatch Staff

Houston, Texas-based Accurate Clinical Research (ACR), a self-described clinical coordinating center, has added a second location on Nassau Bay in Houston, where their new partnering physician has both his clinical practice and research practice.

ACR conducts its own clinical trials and also offers various services to physicians who want to conduct clinical research, including contract and budget negotiation, regulatory, business development, staff training, call center development and patient recruitment. Physicians also have the option of having one of ACR’s certified clinical research coordinators (CRCs) come work at their sites.

Physicians new to clinical research work with ACR for about one year before getting the option to join ACR as partnering physicians or to become principal investigators on their own. Partnering physicians still partake in ACR’s centralized services, including having an ACR-certified CRC come work at their site. They also share in the revenue generated from studies they work on.

Dr. Prashanth Sunkureddi, a rheumatologist, is ACR’s new partnering physician and has worked with ACR for about a year as a sub-investigator. He is working on three active protocols at his site. ACR has 20 active protocols in all, mostly in rheumatology and diabetes, though ACR is multispecialty.

Although contract and budget negotiation is handled by ACR centrally, partnering physicians sit down with the central office and review the budgets together with them.

“Dr. [Philip] Waller and I have set up a strategy where physicians come on board with us here. They see how much paperwork is involved, how much detail is involved in clinical research. They know what’s on the back of a 1572. We’ve hired an elite team that works side-by-side with the physician. And then it’s their choice to stay with us or do it on their own,” said Karen Obmaces, research director at ACR. “We go into each individual physician and set up a strategy for them. We offer them facility setup, study management, regulatory compliance, hiring and training, those types of services.”

Waller, ACR’s medical director/principal investigator, added, “Naive physicians don’t have a clue how to find studies. And when they find them, they ask, ‘What do I do now?’ [ACR] gives them a way to get their feet wet without taking the financial responsibility. We make sure they’re physicians of integrity. Physicians who we put on with us have the ACR stamp of approval. We know they’re physicians who meet our standards.”

ACR has grown since it was established in 2007 from one principal investigator and one coordinator to its current six principal investigators, five certified CRCs and two sub-investigators. “We’re building the original location now as well as our second location with Dr. Sunkureddi,” Obmaces said.

ACR plans to continue adding partnering physicians not only in the Houston area or across Texas but in other parts of the country as well. ACR is debt-free and entirely grant-funded.

“We have a lot of exciting news for 2010,” Obmaces said.

Upcoming Events

  • 12Apr

    The Patient Playbook Webinar Series, Part 3 — Rethinking the Development of Participant-Centric Clinical Trial Technology

  • 25Apr

    Effective Root Cause Analysis and CAPA Investigations for Drugs, Devices and Clinical Trials

  • 26Apr

    FDA’s New Laws and Regulations: What Drug and Biologics Manufacturers Need to Know

  • 27Apr

    Califf’s FDA, 2023 and Beyond: Key Developments, Insights and Analysis

  • 17May

    2023 WCG Avoca Quality Consortium Summit

  • 21May

    WCG MAGI Clinical Research Conference – 2023 East

Featured Products

  • Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

    Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

  • Surviving an FDA GCP Inspection

    Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs

Featured Stories

  • Five Ws

    Consider the Five ‘W’s to Understand Potential Participants

  • QandA-360x240.png

    Perspectives from Smaller-Sized CROs: Q&A with Cheryle Evans

  • White House

    Trial Stakeholders Advise White House on Emergency Research Infrastructure

  • SurveywBlueBackground-360x240.png

    Stress Levels Continue to Climb in Healthcare Workforce, Survey Finds

Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

The information you need to adapt your monitoring plan to changing times.

Learn More Here
  • About Us
  • Contact Us
  • Privacy Policy
  • Do Not Sell or Share My Data

Footer Logo

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

Phone 617.948.5100 – Toll free 866.219.3440

Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing