Clinical Data Manager

Overview
Do you want to make a significant impact in a dynamic organization where you can shape global projects and processes? Are you passionate about working with Clinical Data Management end-to-end with rapid cycles and contributing to an entrepreneurial spirit? If yes, then this might be the perfect opportunity for you!

Essity – a leading global hygiene and health company and the home of brands like TENA, Libresse, Cutimed, Sorbact and JOBST is offering an exciting and challenging opportunity for you who want to contribute with your expertise, energy and creativity. We are looking for an additional colleague to join our company as a Clinical Data Manager in the department of Global Clinical Affairs, within Global Marketing & Innovation (GMI) Global Unit.

Watch our film of why we work at Essity: We are Essity - and we care

About the role
The Clinical Data Manager (CDM) is responsible for how clinical data is collected, managed, and to ensure the quality of clinical data throughout the study. The role also involves managing multiple studies simultaneously, mainly within medical areas such as wound care, incontinence and compression products, but also in other product areas.

Through Clinical Project teams, the CDM is a key contributor in the development of study protocols and to collect data according to regulatory requirements and project goals. The CDM works closely with the Clinical Project Manager and other project members to understand and implement study requirements. They build and configure the Electronic Case Report File (E-CRF) for data collection, and validate and test the system to ensure functionality. The role is also responsible for the study documentation related to data management, e.g. the data management plan. Most of the projects are global, and the CDM assures continuous quality and cleaning throughout the course of the study. Towards the end of the study the CDM is responsible for Clean file and Data Base Lock, extracting the data and delivering data in various formats depending on the recipient. When necessary, the CDM sets requirements and collaborates with external companies, and works on developing and improving work processes.

This is a hybrid role (>50% in the office) that can be based at our office in Gothenburg or Hamburg.

Examples of tasks

• Be the Subject matter expert on Clinical data management throughout a clinical investigation.
• e-CRF programming and set-up.
• Monitor the quality of data throughout the course of a clinical investigation.
• Accountable for all data management related documentation for clinical projects or programs.
• Drive data cleaning activities including data clarifications, data base lock, data extraction etc.
• Establish and maintain a relevant network of vendors (e.g. CROs)
• Ownership of Data Management related processes

Who You Are
You are a person that likes to be an active participant and contributor in all projects. You can explain the rationale behind different approaches and are ready to roll up your sleeves and get things done. You thrive in hands-on project work and have excellent collaboration skills. Your communication abilities are top-notch, allowing you to present and adapt your message clearly based on the audience. You excel at presenting data in a straightforward manner and can manage multiple projects simultaneously. You combine the hands-on work and ability to pay attention to details, with a holistic oversight of the data management across projects and stakeholder.

You have:

• Relevant academic background (preferably MSc or higher)
• Documented experience to manage all aspects of data management, including CRF configuration
• Experience in independent clinical data management in an industry setting (Medical Device, Pharmaceutical or CRO)
• Understanding of applicable rules, regulations, guidelines and industry standards.
• Statistical knowledge is considered a strength.
• Fluency in English

Application
Interested? If you are up for the challenge and think this sounds like you, apply online today! Kindly note that due to GDPR we cannot accept applications via mail.

We may conduct background checks in the final stages of the recruitment process to verify your qualifications and fit for the role

What We Can Offer You
Our purpose, Breaking Barriers to Well-being, provides meaning to everything we do. Working at Essity means a chance to improve well-being for people and opportunities to drive positive change for the society and the environment. As an employee at Essity, you will belong to an organization where you feel valued and supported to grow and challenged to generate business results in a collaborative and open atmosphere.

Innovate for Good | Excel Together | Be You with Us

Application End Date:
21 apr. 2025
Job Requisition ID:
Essity252193