IQVIA

Learning Delivery Quality Lead (Trainer)

Sweden · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

  • EmployerIQVIA
  • LocationSweden
  • Work styleWork style not stated
  • Employment typeFull time
  • Employer posted

Overview

The Learning Delivery Quality Lead is responsible for delivering onboarding, role-readiness, and capability development programs for Clinical Operations staff. This role partners with operational leaders, quality teams, HR, and client stakeholders to ensure employees are appropriately trained, compliant, and prepared to support global clinical research activities.

Key Responsibilities

  • Deliver and facilitate sponsor "Ways of Working" training programs.
  • Lead onboarding and role-readiness programs for Clinical Operations personnel.
  • Coordinate study-specific, process, systems, and compliance training activities with relevant stakeholders.
  • Maintain and enhance role-based training curricula for CRAs, CTAs, Study Managers, Direct Line Managers, and related functions.
  • Conduct training needs assessments and identify capability gaps.
  • Facilitate instructor-led and virtual training workshops.
  • Monitor training compliance and competency metrics.
  • Partner with Operational Leaders, Quality, and HR teams to support workforce capability development.
  • Evaluate training effectiveness and implement continuous improvement initiatives.
  • Support inspection readiness through accurate and complete training documentation.
  • Collaborate with internal and external stakeholders to develop and deploy soft skills training programs.
  • Deliver sponsor Ways of Working training to new hires and existing team members as required.
  • Develop and maintain expertise across the client training landscape, procedural training, monitor training, role-specific training, systems training, therapeutic area learning pathways, and associated documentation.
Show full description

Serve as a subject matter expert and primary point of contact for training-related inquiries from operational teams.

Experience Required

  • Bachelor's degree in scientific discipline or healthcare field.
  • Minimum of 3-5 years' experience in Learning & Development or Training functions within clinical research organizations is required.
  • Minimum of 7-10 years of overall professional experience; prior experience as a Clinical Research Associate (CRA) is preferred.
  • Demonstrated experience working within regulated environments, including ICH-GCP and SOP-driven organizations, is required.
  • Experience using Learning Management Systems (LMS) and training compliance tracking, within Global Pharma, CRO, and FSP environments.
  • Experience developing and delivering instructor-led, virtual, and e-learning programs.
  • Experience managing onboarding and role-based training programs.
  • Experience supporting global or regional clinical trial teams preferred.
  • Minimum 1-2 years of experience delivering training, coaching, mentoring, or onboarding clinical staff.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Staying safe while you apply

  • Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
  • Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
  • Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

  • Check the fit.

    Compare the requirements with the experience you have confirmed, including gaps.

  • Prepare honestly.

    Build interview stories and application drafts from your own evidence.

  • Keep track.

    Save the role and record your own application status and follow-ups.

Create a free workspace or log in.

QA and test engineer jobs in Sweden

ROLIVA currently lists 12 open roles like this in Sweden.

Employers hiring for this

  • Saabgroup3 open roles
  • Elekta2 open roles
  • ABB1 open role
  • AXIS1 open role
  • IQVIA1 open role

Top skills asked for

Listings whose description mentions each term. A mention is not a requirement.

At a glance

  • Employment typeFull time
  • SeniorityLead / Principal
  • Employer posted
  • Added to ROLIVA
  • Last checked

Skills in this posting

Skills ROLIVA found in the employer’s own description above. A mention is not a requirement.

GCP

Explore similar roles

Similar jobs

Anaplan

SDET - AI

London, United Kingdom

Work style not stated