Skip to main content
Post your CV and find your next job on Indeed!

Medical Device Training jobs

Sort by: -
    • Be compliant to trainings and eSOP reading.
    • Reading, United Kingdom | Full time | Home-based | R1562063.
    • Manage end-to-end delivery of data management services…
    • View all IQVIA jobs - Reading jobs - Engineering Team Leader jobs in Reading
    • Salary Search: Data Team Lead, EMEA salaries in Reading
    • See popular questions & answers about IQVIA
  • View similar jobs with this employer
    • 5+ years of relevant experience in the medical device space (either industry or through consulting/service provider).
  • View similar jobs with this employer
    • Significant experience (typically 8+ years) within medical device industry.
    • We are seeking an experienced Medical Device Quality Specialist Consultant to…
  • View similar jobs with this employer
    • This role focuses on advising clients on the regulatory, Quality and compliance aspects of medical devices, through a strong understanding of regulatory and…
  • View similar jobs with this employer
    • Significant experience in medical device and/or drug-device combination product development;
    • This role calls for a senior engineer with substantial experience…
    • Using a smartphone/handheld device to manage your route.
    • Private medical insurance at no cost to you after three months.
    • Up to 90 stops — £100.00.
    • As a Trainee Technician, you will be provided with comprehensive training and development, allowing you to gain valuable experience in the manufacture and…
    • Full product training will be provided.
    • Providing some in-house applications training.
    • Provide high level applications support and training to clinical users.
    • Ensure compliance with relevant medical device and regulatory requirements.
    • Provide product training and commercial support to distributor teams.
    • Under the mentorship of management, responsible for hiring, training, and performance management of staff.
    • Livingston, United Kingdom | Full time | Office-based…
    • Act as a senior strategic advisor to pharmaceutical, biotechnology and medical device clients on HTA evidence planning, market access strategy and reimbursement…
  • View similar jobs with this employer
    • Participate in all required orientation, training, and calibration activities.
    • Hours: Estimated 10–16 hours per month.
    • MD, DO, or PhD preferred.
  • View similar jobs with this employer
    • Participate in all required orientation, training, and calibration activities.
    • Role: Clinical Independent Rater for Clinical Trials.
    • MD, DO, or PhD preferred.
    • Under the mentorship of management, responsible for hiring, training, and performance management of staff.
    • Livingston, United Kingdom | Full time | Office-based…
    • You will be responsible for services including patient-specific cranioplasty implants, anatomical modelling, specialist mechanical engineering, medical device…
Data Team Lead, EMEA
IQVIA
·
3.7
Reading
•
Remote
Full-time
Apply on company site

Job details

Here’s how the job details align with your profile.

Job type

Full-time

Benefits

Pulled from the full job description
Employee stock ownership plan
Work from home

Full job description

Reading, United Kingdom | Full time | Home-based | R1562063


Job Overview



Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables. Perform role of Data Team Lead (DTL).

Essential Functions



  • Gather Study Set up requirements through discussion and communication with relevant stakeholders.
  • With Minimal guidance - support, overview of validation of new Device integrations.
  • Oversight & Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.
  • Ensure that all the deliverables are of expected quality standards and meet customer expectations.
  • With guidance, ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW).
  • Support Training of New joiners.
  • Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.
  • Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended as required.
  • With Guidance manage & oversight the implementation of new technology / database revisions.
  • Work closely with the programming team for process innovation and automation.
  • Be compliant to trainings and eSOP reading.
  • Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
  • Communication with Line Manager, and other team members across functions should be collaborative.
  • Perform other duties as directed by Line Manager.

Qualifications



  • Bachelor's Degree In health, clinical, biological or mathematical sciences, or related field with proven experience in Data Management Req
  • 3 -4 years direct Data Management experience, including a minimum of 1 year as a CDM project lead. Pref
  • English Fluency Spoken and English Advanced
  • Advanced computer applications like Microsoft excel, word, Inbox etc Advanced
  • Should have Advanced understanding of Drug development lifecycle and Overall Clinical research process Advanced

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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.


Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Let Employers Find YouUpload Your Resume