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IQVIA

Runs drug trials and sells health data to pharma

Associate Business Development Director - Safety Solutions

Account ExecutiveConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A sustained and successful track record of at least six years selling professional services to pharmaceutical, biotechnology, medical device, and/or clinical research organizations is required.
  • A demonstrated track record of success working with senior-level management in a fast-paced growth environment is required.
  • Full sales-cycle experience is required, including prospecting, identifying opportunities, proposing solutions and writing proposals, negotiating, and closing.
  • Strong written and verbal English skills and experience with quality-oriented proposal writing and proposal management are required.
  • A bachelor's degree or higher is required.
  • Applicants must be willing to travel throughout the United States, estimated up to 50%.
  • Applicants must reside in the greater Boston area, NY/NJ area, VA/DC metro area, or California.

Responsibilities

  • Prospect accounts focused on Safety and Regulatory products and services.
  • Identify and develop new accounts and follow up on existing leads.
  • Develop and maintain productive relationships with key target accounts.
  • Manage assigned accounts to generate incremental and repeatable annual business.
  • Initiate and manage Requests for Information and Requests for Proposals, and negotiate terms for account programs and projects.
  • Work collaboratively with the Professional Services Organization to ensure complete and professional delivery of software and service solutions.
  • Expand sales of the product portfolio in the Safety and Regulatory market.
  • Collaborate with executives and subject-matter experts to maximize account coverage.
  • Maintain a knowledgeable understanding of changing regulatory guidelines and mandates affecting the industry community.
  • Conduct full-cycle sales, including identifying targets, securing and managing client meetings, understanding client needs, addressing concerns and objections, coordinating subject-matter experts to define opportunities, proposing solutions, negotiating, obtaining Statements of Work, and closing deals.

Desired Qualifications

  • Understanding of the regulatory pharmacovigilance process for both pre-marketed and post-marketed product stages.
  • Experience selling drug safety consulting services and products.
  • Experience working with Regulatory Affairs departments, product safety-related departments, or regulatory submissions.
  • Background in the Software as a Service market.
  • Experience with data-mining or statistical signal detection products.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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