Specialist, CTSM IRT Systems

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Mainz, Germany; London, United Kingdom; Munich, Germany | full time | Job ID: 9651

Overview

As a Specialist, CTSM IRT Systems, you will play a key role on the frontier of clinical trial supply management, supporting the setup and maintenance of Interactive Response Technology (IRT) systems globally for our innovative Phase I-III clinical trials. You’ll work closely with cross-functional teams and pioneering partners to ensure the seamless delivery of cutting-edge solutions, accelerating our journey from science to survival.

Responsibilities

• Serve as a critical collaborator in communicating study parameters to IRT vendors under the guidance of the IRT Manager.
• Coordinate IRT system setup and ongoing maintenance, including User Requirement Specification (URS) reviews and User Acceptance Testing (UAT).
• Assist in preparing UAT test scripts, participate in testing activities, and identify risks within system configurations.
• Act as a key contact for budget management and category-invoice workflows.
• Support user training by developing training materials and guiding users on system functions.
• Maintain the integrity of essential documentation by uploading materials to the electronic Trial Master File (eTMF).
• Provide basic IRT-related communication and support to vendor teams, fostering effective collaborations.

What You Have to Offer

• Bachelor’s degree in Computer Science, Information Systems, Life Sciences, Engineering, or related discipline.
• Foundational professional experience (minimum 3 years) with exposure to clinical trial supply management or related areas in the pharmaceutical industry preferred.
• Knowledge of clinical supply chain processes and relevant GMP/GDP guidelines.
• Familiarity with IRT systems and IT-system validation/testing activities.
• Strong skills using Microsoft Office (Word, Excel, PowerPoint).
• Excellent communication skills and a proactive approach to overcoming challenges.
• Business-level fluency in English.

What We Do

We develop the first modular mRNA manufacturing facilities based on a container solution called “BioNTainers” to improve healthcare worldwide. Help us build a regional manufacturing network in Africa & Australia: with the region and for the region. As part of the local team, drive the establishment of regional end-to-end mRNA manufacturing solutions.

Benefits

BioNTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base. We offer competitive remuneration packages determined by the specific role, location of employment, and the selected candidate’s qualifications and experience. Availability, eligibility and design of listed benefits may vary by location and internal policy.

How to apply

Apply now by sending your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter, and contact details via our online form.

Please note: Only applications sent via our online form shall be considered. By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through HireRight. You will be informed accordingly by your BioNTech-Recruiter.

Job details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Information Technology

We are looking forward to receiving your application.

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