• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • COVID-19 Patient Resource Center
    • Clinical Trials
    • Search Clinical Trials
    • Patient Notification System
    • What is Clinical Research?
    • Volunteering for a Clinical Trial
    • Understanding Informed Consent
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Clinical Trial Listings
    • Market Research
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • JobWatch
    • White Papers
    • SOPs
    • eCFR and Guidances
  • White Papers
  • Trial Listings
  • Advertise
  • COVID-19
  • iConnect
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » ACRP, DrugDev partner to increase visibility of clinical researcher and site profiles

ACRP, DrugDev partner to increase visibility of clinical researcher and site profiles

April 26, 2017
CenterWatch Staff

The Association of Clinical Research Professionals (ACRP) and DrugDev announced a partnership to radically decrease clinical trial investigator burden. The two organizations have partnered together to offer ACRP clinical researchers and site staff members online profiles visible to premier pharma companies and CROs. These companies and CROs represent more than one-third of all clinical trials today and will support ACRP members' needs for faster, more efficient site selection. This achievement is made possible by the DrugDev Profiles System, which uses the DrugDev Golden Number to match and master site facilities and personnel information.

ACRP is the first organization to launch a partnership with DrugDev offering online profiles to clinical researchers.

All sponsors and CROs who use DrugDev services for study planning and site identification will be able to view investigator sites and personnel profiles from ACRP members.

About 80% of sites maintain an online profile to decrease burden during feasibility and startup. Additionally, online profiles allow sites to provide their information once, instead of at the start of each new trial.

While these advances help, online profiles are still a significant source of investigator burden. The DrugDev 2016 Global Investigator Survey found that 35% of sites have at least three online profiles, and nearly 10% maintain 11 or more profiles. These data suggest that finding a way to increase collaboration industry-wide is critical for investigators to participate in clinical trials.

In 2014, the profiles module of DrugDev Spark launched in partnership with Investigator Databank with the goal of driving industry-wide collaboration and decreasing the burden associated with online profiles, feasibility, site identification, and site startup. Study sponsors can access site profiles through DrugDev Spark modules and users can quickly and easily export their Profile as a standard format CV to share with any CRO or sponsor. The result is a win-win, matching the right sites with the right studies and decreasing site burden while increasing visibility for study opportunities.

"Partnering with DrugDev to increase the visibility of ACRP members and their organizations supports our mission to promote excellence in clinical research," said Jim Kremidas, ACRP executive director. "We are excited about this unique opportunity to provide additional value to our members."

Elisa Cascade, president of Data Solutions at DrugDev, explained, "DrugDev is passionate about technology that improves the site experience, and partnering with ACRP on online profiles is a great example of how we are using collaboration and standardization to reduce clinical researcher burden. Moreover, making investigator and site profiles available to the multiple CROs and sponsors who use the DrugDev platform reduces the number of basic site information requests. This in turn allows investigators to spend less time on repetitive administrative tasks and more time focused on clinical activities. It also allows the CROs and sponsors to target their study opportunities better to the right sites."

Upcoming Events

  • 24May

    Powering an Effective Oversight Strategy with Clinical and Operational Insights

  • 25May

    2022 WCG Avoca Quality & Innovation Summit: Own the Future

  • 28Jun

    Effective Root Cause Analysis and CAPA Investigations for the Life Sciences

  • 16Oct

    WCG MAGI's Clinical Research Hybrid Conference - 2022 West

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

  • Protocol-360x240.png

    Avoid Deviations by Making Protocol Review a Team Effort

  • SelectionProcess-360x240.png

    Give Us a Voice: Sites Clamor for a Say on Vendor Selection

  • Convince-360x240.png

    Use Data and Details to Convince Site Leadership to Add Staff

  • AsktheExpertsBadge-360x240.png

    Ask the Experts: Listing Trial Staff and Others on the Statement of Investigator

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 My Personal Information

Footer Logo

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

Phone 617.948.5100 – Toll free 866.219.3440

Copyright © 2022. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing