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CluePoints

Cloud-based RBQM platform for clinical trials

Sales Enablement Manager

Sales OperationsConfirmed live in the last 24 hours
Full-timeUnited KingdomNo salary listed

About the Job

Requirements

  • Experience in a sales enablement, sales operations, or similar role within a B2B software-as-a-service environment.
  • A track record of building or reorganising sales playbooks and field-facing content that sales representatives adopt.
  • Experience designing and running onboarding or ramp programmes for a sales team.
  • Strong stakeholder management skills and comfort working cross-functionally across Sales, Marketing, and Product.

Responsibilities

  • Organise and structure existing sales content into a clear, easy-to-navigate playbook that the whole team can find and use.
  • Own and maintain battlecards, objection-handling guides, and competitive-positioning material, keeping them current as the market evolves.
  • Build and run onboarding ramp plans for new sales hires, plus ongoing coaching, reinforcement, and skill-gap interventions for the existing team.
  • Identify training and content gaps across the sales team and brief the instructional designer on what needs to be built.
  • Own content structure and adoption within Docebo, track usage data to understand what is landing with sales representatives, and act on what is not.

Desired Qualifications

  • Direct experience with Docebo or a comparable learning management system or sales enablement platform.
  • Experience in clinical trials, life sciences, or another regulated software-as-a-service environment.
  • Experience briefing or managing instructional designers or other learning and development contractors.

About the Company

CluePoints

Cloud-based RBQM platform for clinical trials

CluePoints provides risk-based quality management and data quality oversight software for clinical trials. Its cloud-based platform analyzes trial data using advanced statistics, machine learning, and AI to identify risks and monitor data quality from initial risk assessment through issue tracking. Key products—Site Profile and Oversight Tool (SPOT), Intelligent Medical Coding (IMC), Intelligent Query Detection (IQD), and Medical & Safety Review (MSR)—automate data discrepancy detection, improve medical review efficiency, reduce manual coding, and enable adaptive site monitoring. The company differentiates itself with an end-to-end, multi-product platform (expanded in 2024) that combines RBQM, data analytics, and regulatory-aligned monitoring to help pharmaceutical/biotech companies and CROs de-risk trials and ensure data integrity and patient safety. Its goal is to help customers meet regulatory guidance from bodies like the FDA and EMA while improving trial quality and efficiency.

Company size
201-500
Company stage
Acquired
Total funding
$6.6M
Headquarters
Ottignies-Louvain-la-Neuve, Belgium
Founded
2012

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