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Company Overview

Tom Hanley and Brant Smith, two graduates of Rensselaer Polytechnic Institute, founded Smith Hanley in 1980 and grew it to a professional staffing business with offices in five U.S. metropolitan areas, including New York, Southport, Chicago, Houston, and Orlando.

In 2004, Smith Hanley was acquired by inVentiv Health (NASDAQ: VTIV), the leading provider of commercialization and complementary services to the global pharmaceutical, life sciences, biotechnology, and other industries. inVentiv delivers its customized clinical, sales, marketing, and communications solutions through its three core business segments: inVentiv Clinical, inVentiv Communications, and inVentiv Commercial.

Smith Hanley Consulting Group remains committed to the one-on-one relationships that began with our establishment nearly 30 years ago, and we now have the security and credibility that represent being a part of a large, publicly-traded corporation.

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Job Description

Sample Accountability Sr. Analyst

Job Duties:

  • Bring your organizational skills and detail-orientation to this exciting role in Pharmaceutical Sales Operations. Specific focus will be to ensure compliance in sample administration.

  • Serve as sales operations liaison with compliance and regulatory personnel as well as federal agencies.

  • Ensuring sample systems meet the business needs.

  • Interaction and collaboration with vendors to include service level assessments and contract obligations.

  • Develop field communications and project plans surrounding sample management

 

Benefits available:

  • Competitive salaries
  • Multiple medical / dental plans
  • Long term disability
  • 401k savings plan
  • Company Paid Life Insurance
  • Long term Disability

 



Job Requirements

Sample Accountability Sr. Analyst

Job Requirements:

  • 5-8 years experience in sales operations
  • 3-5 years focused experience in sample accountability
  • Ability to multi-task and prioritize in ambiguous environment will be key to success
  • Exceptional and proven verbal and written skills
  • Extensive Knowledge of PDMA and FDA/DEA requirements regarding sample management, controlled substance sampling administration and education
  • Knowledge of 21 CFR Part 11 Compliance and Systems Validation
  • Strong capabilities and use of Microsoft Office (Word, Excel and PowerPoint)
  • Professional degree highly preferred.

 

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