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Clinical Programs Director, Data Intelligence

Job in Fall River, Bristol County, Massachusetts, 02720, USA
Listing for: Danaher Corporation
Full Time position
Listed on 2026-05-30
Job specializations:
  • IT/Tech
    Data Analyst, Data Science Manager, Business Systems/ Tech Analyst
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cytiva, one of Danaher’s () 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.

Learn about the Danaher Business System () which makes everything possible.

The Clinical Programs Director, Data Intelligence leads the creation and deployment of intelligent, data‑driven solutions that connect Salesforce with external molecule data to automate workflows, improve visibility, and strengthen operational performance. This role plays a critical part in advancing the Molecule Tracking Growth Room initiatives by streamlining and accelerating the spec win to design in process. The role will directly influence Cytiva’s ability to secure specification positions and expand market share in high‑value drug development workflows.

This role reports to the Director, Clinical Programs Platforms and Strategy and sits within the Clinical Programs organization, based in Marlborough, Massachusetts, supporting initiatives across a global footprint.

What you will do:
  • Lead the CRM Analytics roadmap for Design In, ensuring alignment with Clinical Programs strategy and commercial growth objectives while integrating Salesforce with external molecule datasets to enhance automation and visibility.

  • Provide technical and strategic leadership on AI driven tools that support molecule tracking, lifecycle management, and advanced analytics to accelerate specification wins.

  • Serve as the primary liaison with external analytics and technology partners, driving collaboration and successful delivery of data‑driven solutions.

  • Oversee the full development lifecycle—including solution design, prototyping, implementation, testing, deployment, and ongoing optimization—to deliver scalable analytics capabilities.

  • Deliver monthly Policy Deployment reporting, translating performance insights into clear, actionable recommendations for leadership.

Who you are:
  • Bachelors degree in a scientific, technical, or related field. Masters degree preferred.

  • Deep experience with Salesforce, CRM Analytics (Tableau CRM/Einstein), SQL, and modern Microsoft tools, including Copilot and emerging AI platforms.

  • Demonstrated ability to design and execute CRM and data strategies supporting complex analytics, reporting, and workflow automation at scale.

  • Exposure to AI/ML tools with the ability to translate technical outputs into practical business applications for molecule tracking and lifecycle insights.

  • Strong analytical, problem solving, communication, and stakeholder‑management skills, with the ability to operate both strategically and hands on to build, test, and optimize solutions.

Travel Requirements:
  • 25% travel to EMEA, USCAN, and APAC
It would be a plus if you also possess previous experience in:
  • Hands on experience with biotherapeutic drug development, molecule progression, or process development, with the ability to tie scientific workflows to commercial and operational decisions.

  • Familiarity with Global Data, clinical program management systems, and external molecule databases, with the ability to synthesize these sources into actionable insights.

  • Proven success navigating complex, global, matrixed organizations and driving alignment across commercial, scientific, and technical stakeholders.

  • Experience leading cross functional digital or…

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