to lead the planning, development, and implementation of our Quality-Controlled Trial Management System (QCTMS). This role is essential to ensuring the successful configuration and customization of QCTMS for clinical studies in a regulated environment.
Responsibilities
Planning and managing QCTMS development, testing, and documentation
Providing technical consultancy during study configuration and customization
Ensuring compliance with internal SOPs and regulatory standards
Lead the planning and execution of QCTMS development and testing activities
Define release-specific requirements and oversee release planning
Provide technical support to Study Project Managers during:
Study-specific requirements analysis
Configuration planning
System customization (interfaces, integrations, etc.)
Review and validate study configurations
Perform activities in accordance with QCTMS SOPs
Requirements
Bachelor or Master’s degree in IT, natural sciences, or equivalent qualification and experience
Proficiency in SQL
for data querying, validation, and troubleshooting within QCTMS databases.
QCTMS functionality and workflows
Software project management, especially in regulated environments
Familiarity with XML, JavaScript
Python, R programming knowledge is beneficial
Thank you for submitting your application. We truly appreciate your interest in joining our company.
Please note that the review process may take some time. If you are selected to move forward, we will contact you within two weeks. If you are not selected, please understand that we will not be sending additional updates.
In accordance with the application procedure (Art. 6 para. 1b GDPR), we will retain your application documents for a period of six months. After this time, your data will be securely deleted. You have the right to request access to, rectification, or deletion of your personal data, to restrict or object to its processing, and to request data portability.
If you have any questions regarding data protection, please contact our Data Protection Officer at dataprotection@gcp-service.com.
We wish you all the best in your job search.
Best regards,
HR team @ GCP-Service International
If we have piqued your interest, we look forward to receiving your application. Please address it as follows, stating your salary expectations and the earliest possible starting date:
GCP-Service International Ltd. & Co.KG
Anne-Conway-Str. 2
28359 Bremen Germany
E-mail: application@gcp-service.com
Location: Bremen, Germany
We are seeking a skilled and proactive
QCTMS Manager
to lead the planning, development, and implementation of our Quality-Controlled Trial Management System (QCTMS). This role is essential to ensuring the successful configuration and customization of QCTMS for clinical studies in a regulated environment.
Responsibilities
Planning and managing QCTMS development, testing, and documentation
Providing technical consultancy during study configuration and customization
Ensuring compliance with internal SOPs and regulatory standards
Lead the planning and execution of QCTMS development and testing activities
Define release-specific requirements and oversee release planning
Provide technical support to Study Project Managers during:
Study-specific requirements analysis
Configuration planning
System customization (interfaces, integrations, etc.)
Review and validate study configurations
Perform activities in accordance with QCTMS SOPs
Requirements
Bachelor or Master’s degree in IT, natural sciences, or equivalent qualification and experience
Proficiency in SQL
for data querying, validation, and troubleshooting within QCTMS databases.
QCTMS functionality and workflows
Software project management, especially in regulated environments
Familiarity with XML, JavaScript
Python, R programming knowledge is beneficial
Thank you for submitting your application. We truly appreciate your interest in joining our company.
Please note that the review process may take some time. If you are selected to move forward, we will contact you within two weeks. If you are not selected, please understand that we will not be sending additional updates.
In accordance with the application procedure (Art. 6 para. 1b GDPR), we will retain your application documents for a period of six months. After this time, your data will be securely deleted. You have the right to request access to, rectification, or deletion of your personal data, to restrict or object to its processing, and to request data portability.
If you have any questions regarding data protection, please contact our Data Protection Officer at dataprotection@gcp-service.com.
We wish you all the best in your job search.
Best regards,
HR team @ GCP-Service International
If we have piqued your interest, we look forward to receiving your application. Please address it as follows, stating your salary expectations and the earliest possible starting date:
GCP-Service International Ltd. & Co.KG
Anne-Conway-Str. 2
28359 Bremen Germany
E-mail: application@gcp-service.com
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