Mainz, Germany; London, United Kingdom | full time | Job ID: 9810
As Associate Director Global Clinical Development Operations (GCDO) Data & Business Systems, you will play a key role in establishing, maintaining, and continuously improving our Clinical Trial Management systems and processes. You will work collaboratively with cross-functional teams to ensure successful project outcomes and provide operative support to end-users.
Your Main Responsibilities Are:
* Co-develop and maintain GCDO systems, with a focus on Clinical Trial Management Systems (CTMS) and related interfaces
* Collaboratively or individually, plan and execute capability-related projects to deliver business value.
* Collaborate with stakeholders to identify business needs and gapsand implement system enhancements & coordinate releases
* Ensure system configurations align with GCDO processes and regulatory requirements
* Provide user training and guidance to clinical teams to enhance system adoption and utilization
* Monitor system performance and troubleshoot operational issues to ensure seamless functionality
* Evaluate and implement technological solutions to support clinical trial conduct, focusing on Veeva Clinical Vault and analytics tools
* Plan and execute capability-related projects to deliver business value
* Act as a quality gate for clinical systems and provide operational support to end-users
* Establish measures to ensure data integrity, accuracy, and accessibility within GCDO systems
* Define, optimize and enforce data flows, governance standards, policies, and best practices
What You Have To Offer:
* Bachelor’s degree or higher in natural or life sciences
* Minimum of 5 years of proven track record in similar functions
* Strong understanding of clinical trial operations, regulations, and compliance requirements
* Ability to work independently and in international cross-functional project environments
* Excellent communication and interpersonal skills to collaborate with diverse stakeholders
* Analytical mindset and attention to detail for accurate data management
* Proficiency in database management and Microsoft Office suite; knowledge of Veeva Clinical Suite is an asset
* Adaptability and strong organizational and time-management abilities.
* Fluency in English (written and spoken); German is optional
Your 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 which is determined by the specific role, location of employment and also the selected candidate’s qualifications and experience.
Note: The availability, eligibility and design of the listed benefits may vary depending on the location. The final requirements for the individual use of our benefits are based on the company's internal policies and applicable law.
How to apply:
Apply now by sending us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your 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 our service provider ‘HireRight’. You will be informed accordingly by your BioNTech-Recruiter.
We are looking forward receiving your application.