• 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 » Oncologists restrict pharmaceutical sales rep access at accelerating rates

Oncologists restrict pharmaceutical sales rep access at accelerating rates

August 29, 2012
CenterWatch Staff

As more pharmaceutical companies prepare to bring new oncology drugs to market, their sales representatives face a rising hurdle—oncologists are reducing the number of times they will see them.

According to the spring 2012 AccessMonitor, a report from global sales and marketing consulting firm ZS Associates, about 61% of oncologists placed moderate-to-severe restrictions on visits from pharmaceutical sales reps. This makes oncology the most restrictive of the 20 most common medical specialties measured in the report. By comparison, about 47% of cardiologists and only 38% of primary care physicians restrict rep access to the same degree.

Oncology is the fastest-growing specialty therapy area in the world and accounted for 10 percent of global pharmaceutical sales in 2011. Currently, there are about 1,000 oncology drugs in the pipeline—almost twice the number in any other field.

"Sales reps equip oncologists with data on evolving science, access to financial assistance for patients, and help with reimbursement support and patient support materials," said Ganesh Vedarajan, principal and leader of the oncology and specialty therapeutics practice at ZS Associates. "Regulatory constraints, however, are increasingly restricting these offerings. Physicians also are able to access scientific data in real time through other channels."

Vedarajan continued, "While oncologists still see some value in rep visits, increased patient load and more time spent on reimbursement issues limit the time they have available. Most practices now require reps to schedule appointments in advance—and generally provide only two or three potential openings per week."

The report examined how often 350,000 physicians and other prescribers meet with pharmaceutical sales representatives who visit them. It then classified those doctors into one of three groups: "accessible" (physicians who met with more than 70% of reps); "access restricted" (physicians who met with 31%-70% of reps); and "severely access restricted" (physicians who met with no more than 30% of reps).

According to the report, only 39% of oncologists were "accessible," compared to 65% of all prescribers. Moreover, 11% of oncologists placed severe access restrictions on reps, compared to just 9% of all prescribers. About half of oncologists placed moderate access restrictions on reps compared to 26% of all physicians.

"While reach seems to have stabilized, the frequency with which an oncologist will see a rep has declined at a steady pace," said Jon Roffman, associate principal and leader of the oncology practice's field force strategy work. "For the first time since AccessMonitor began tracking physician access in 2006, oncologists who placed moderate-to-severe restrictions on rep visits outnumbered those with relatively few access restrictions."

According to AccessMonitor, an overwhelming majority of oncologists (79%) saw even their best reps only up to 12 times each year—and almost no specialists allowed reps to visit them more than 24 times per year. This compared to 3% of primary care physicians and 13% of all specialists who will meet with their best reps more than 24 times a year.

"With the increasing number of approved oncology drugs and the active pipeline, properly introducing these therapies to physicians is going to get more complicated. Indeed, within just a few years, the average rep may be unable to meet with a doctor face-to-face more than four times each year," said Roffman. "It's hard to be effective with so little interaction. To meet this challenge, pharmacos must rethink their approach to engaging with this physician group. Both the offering and selling model must dramatically shift to adjust to the constraints and needs of oncologists."

Because many oncologists limit the number of times they see any single rep each year, pharma companies are tempted to secure more doctor visits by sending several different reps to promote the same drug.

"These conditions are ripe for a new pharma sales rep 'arms race,'" said Vedarajan. "Pharma companies that hire more reps must be careful not to overwhelm prescribers with sales calls."

This is why Maria Whitman Mumm, associate principal and leader of East Coast marketing solutions in the oncology practice at ZS Associates, encourages companies to focus on the customer experience. "This requires a mind shift for pharmacos," said Whitman Mumm. "Instead of designing their field organization based on, 'How many sales reps do I need?' pharmacos should ask, 'What is the physician experiencing, and how can I help improve the experience by bringing the most value to him or her?'"

According to Whitman Mumm, sales reps must understand the physician's needs and preferences and use a mix of services and tactics—including new technologies—to improve the overall experience. Pharmacos must also encourage reps to remain at the center of communication and provide a personal touch to these doctor interactions where possible. ZS research, in fact, indicates higher physician open rates for emails sent by reps compared to those sent by the head office.

"The sales model also must evolve to take a different sales approach to institutions," added Vedarajan. "Some institutions do not allow sales reps at all. As the industry consolidates and more physician practices are acquired by institutions, this problem will become worse. Companies should think about steps to adapt for continued success."

Upcoming Events

  • 12Apr

    The Participant 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