0Full-time Clinical Data Manager (IRT) Clinical Trials (m/f/d)
expertum GmbH | Germany | 88400 Biberach an der Riß | Home office | Published since: 08.01.2026 on stepstone.de

Full-time Clinical Data Manager (IRT) Clinical Trials (m/f/d)


Are you looking for a new professional challenge?

Then you're right with us. As a staff expert, we support various companies in finding appropriate specialist and executives (m/w/d) and are at your side as a career advisor.

Our client is a well-known company from the pharmaceutical industry with several locations in Germany. We are currently looking for you at the location Biberach at the crack for the following attractive position,

Senior Account Manager (m/w/d)

Take advantage of your chance and become part of this success story! !

Your tasks • Your profile • What we offer

Are you looking for a new professional challenge?

Then you're right with us. As a staff expert, we support various companies in finding appropriate specialist and executives (m/w/d) and are at your side as a career advisor.

Our client is a well-known company from the pharmaceutical industry with several locations in Germany. We are currently looking for you at the location Biberach at the crack for the following attractive position,

Senior Account Manager (m/w/d)

Take advantage of your chance and become part of this success story!

This position is a hybrid working model which can be covered from the Home Office/remote on 2 to 3 days per week after consultation or as required. The incorporation takes place on site. In this new role, you will independently conduct all activities consisting of evaluation, planning, conceptual implementation and implementation as well as review, maintenance and decommissioning of study-specific IRT concepts. You act independently as IRT representatives in cross-departmental and cross-functional study and project teams and have sound expertise in the technical implementation of IRT concepts and clinical study design with regard to compliance and drug safety. You also contribute to the continuous development of IRT concepts by introducing new approaches and solutions to keep the systems up-to-date. You ensure that all work is carried out taking into account patient safety and in accordance with GMP and GCP as well as US, EU and other international guidelines.

Additional tasks for the expert role: You support the activities for validating computer-assisted systems.

IRT Specialist: Master's degree in natural sciences and several years of experience in a related scientific discipline or Bachelor's degree with many years of experience in a related field or experience in quality environment. IRT experience, proven in-depth knowledge of the technical aspects and functions of an IRT system (of advantage). Good knowledge of the generic software development cycle, including the validation of cloud systems (of advantage). Good knowledge of regulatory requirements and GMP/GCP requirements in the pharmaceutical industry and their application to the function are required. Good knowledge of global investigative drug activities as well as general clinical study and design. Ability to initiate and analyze complex tasks independently, taking into account the applicable regulations, economics and timetables. Excellent communication skills and fluent in English, both in word and in writing.

IRT Expert: Master's degree in natural sciences and several years of experience in a related scientific discipline or Bachelor's degree with many years of experience in a related field or extensive experience in quality environment. IRT experience, proven deep knowledge of the technical aspects and functions of an IRT system. Good knowledge of the generic software development cycle, including the validation of cloud systems. Good knowledge of regulatory requirements and GMP/GCP requirements in the pharmaceutical industry and their application to the function are required. Good knowledge of global investigative drug activities as well as general clinical study and design. Ability to initiate and analyze complex tasks independently, taking into account the applicable regulations, economics and timetables. Excellent communication skills and fluent in English, both in word and in writing.

We pay a collective salary and if necessary Industry supplements, holiday and Christmas allowances as well as shift allowances according to the GVP tariff agreement based on the chemical collective agreement Your employment contract is unlimited. In cooperation with Allianz and the Nuremberg Insurance, we offer an occupational pension scheme. You get a high-quality professional equipment for protective and workwear as well as medical precautions by the Werksarztzentrum. If necessary, we finance individual training courses that will continue to take you in the long term. As an expert employee, you get exclusive discounts in over 600 shops and online shops. We will also be happy to advise you on other advertised positions and career opportunities. Section 1075

Location

ava expertum GmbH
88400  Biberach an der Riß
Germany

The text of this ad was translated from German into English using an automatic translation system and may contain semantic and lexical errors. Therefore, it should be used for introductory purposes only. For more detailed information, see the original text of the ad at the link below.

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