Demo

Director, Consulting

BioIVT
Detroit, MI Full Time
POSTED ON 4/21/2025
AVAILABLE BEFORE 5/19/2025

Job Description

Job Description

BioIVT is a leading global provider of high-quality biological specimens and value-added services. The company specializes in control and disease state samples including human and animal tissues, cell products, blood, and other biofluids. BioIVT’s unmatched portfolio of clinical specimens directly supports precision medicine research and the effort to improve patient outcomes by coupling comprehensive clinical data with donor samples and specialized ADME-Tox and drug transporter research services.

The company is organized into 4 business units (Normal Human and Animal, Disease State, ADME-Tox, and Immune Cell). For over 25 years, BioIVT has been the leading global provider of clinical specimens to support drug discovery through development applications.

In October of 2021, BioIVT partnered with Linden Capital, a Chicago-based healthcare private equity firm, to help drive continued growth and expansion for the business.

About Linden Capital : Founded in 2004, Linden Capital is the country’s largest dedicated healthcare private equity firm creating exceptional value for companies, business owners and investors. Linden Capital, headquartered in Chicago, Illinois has invested more than $3 billion in healthcare companies, helping to build strong platforms, and thriving businesses. Over the course of the company’s history, they have helped to build a portfolio of companies into sector market leaders, garnering exceptional returns for investors and companies.

Summary

The Director of Consulting at BioIVT will report to the VP of Scientific Consulting and provide expert guidance on in vitro drug-drug interaction (DDI) studies and regulatory strategies. This role involves conducting gap analyses, designing studies, and formulating responses to regulatory agencies based on current guidance. While the primary focus is small molecule development, consulting projects may extend to novel therapeutics, including antibody-drug conjugates, peptides, and oligonucleotides.

Key responsibilities include scientific data review, client consultation, regulatory strategy development, and public scientific engagement. The Director will collaborate closely with Sales, Scientific Operations, and Marketing to ensure technical fluency across teams, support sales enablement, and identify opportunities for innovation and growth.

The ideal candidate holds a doctoral degree in a relevant field, possesses extensive post-doctoral experience in ADMET, and demonstrates strong scientific, regulatory, and business acumen.

Duties and Responsibilities

Scientific Consulting & Client Engagement

  • Conducts gap analyses and consulting on in vitro DDI studies, advising clients on study design and regulatory strategy.
  • Reviews scientific and regulatory data, writing and presenting detailed analyses of DDI-related questions.
  • Leads client meetings and video calls, delivering high-quality consulting services and ensuring alignment with regulatory expectations.
  • Assists in developing study protocols based on consulting recommendations.
  • Presents scientific insights at industry conferences, webinars, and other public forums to enhance BioIVT’s thought leadership.

Sales Enablement & Business Development

  • Supports the sales team by participating in technical discussions, presentations, and client training.
  • Develops white papers, blogs, and other technical content to build brand awareness and generate leads in alignment with Marketing campaigns.
  • Proactively engages with prospective clients to identify consulting opportunities and expand BioIVT’s ADMET service offerings.
  • Builds and maintains a network of key opinion leaders, strengthening BioIVT’s presence in the scientific community.
  • Supports the revenue goals of the business unit through pro-active outreach to prospective clients for consulting opportunities. Actively seeks out scientist to scientist conversations that bring value to BioIVT and our clients
  • Internal Scientific Leadership

  • Serves as a subject matter expert (SME) in research and regulatory areas relevant to BioIVT’s business.
  • Stays abreast of emerging scientific and regulatory trends, identifying opportunities for new services or technology investments.
  • Collaborates with Operations, Project Management, Marketing, and Sales to drive innovation and scientific excellence.
  • Qualifications

  • Doctoral degree (e.g., Ph.D., D.Sc., Sc.D., etc.) in pharmaceutical sciences, pharmacology, toxicology, pharmacometrics or a related field plus seven or more years’ post-doctoral experience in ADMET areas relevant to in vitro DDI required.
  • Ideal candidates will have expertise beyond small molecule development and have familiarity with novel therapeutics, including antibody-drug conjugates, peptides and oligonucleotides.
  • Demonstrated excellence in both written and oral communication skills with track-record of public speaking engagements and scientific publications.
  • Knowledge of FDA, EMA and International regulations and guidance, and industry best practices related to drug preclinical drug development.
  • Good understanding of business and corporate strategy relating to drug research, development, submissions, approvals process and other regulatory matters, and has an excellent overall grasp of issues relating to the pharmaceutical industry.
  • Excellent understanding of elementary chemical, biochemical and / or cell biology principles. Detailed knowledge of scientific terminology.
  • Proficient in programs including Microsoft Word, Excel, PowerPoint and Outlook.
  • Knowledge of customer relationship management (CRM) and prospecting tools is preferred.
  • Strong collaboration, time management, organizational and interpersonal skills
  • Passion for working directly with clients and providing solutions to drive customer success and improve their experience.
  • Ability to work as part of, and lead, cross-functional teams involving Operations, Project Management, Marketing, and Sales and effectively engage at all levels of the organization, including senior leadership.
  • Ability and willingness to travel (up to 20%) as necessary, including overnight business trips.
  • We offer a comprehensive benefit package for eligible team members including medical, dental, vision, short-term / long-term disability, life insurance, hospital indemnity and accident insurance. We also offer a generous retirement plan with a company match. Eligible employees also enjoy competitive time-off policies. We are a collaborative environment that promotes growth from within. Enjoy company-sponsored events for the entire team!

    We can’t wait to work with you!

    We are an equal opportunity employer.

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