Manager*/ Associate Director* Clinical Operations Capabilities
Open for hire at one of the following locations – Mainz Goldgrube. - Job ID: 6957
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Manager*/ Associate Director* Clinical Operations Capabilities
The Manager*/Associate Director* Clinical Operations Capabilities is responsible for the development and maintenance of Clinical Operations capabilities, optimizing Global Clinical Development Operations processes, managing certain technology capabilities and systems (such as CTMS, SSU, etc.) by operationally controlling those. Project management is an important asset in the GCP environment whilst fostering on continuous improvement at any given time. The Manager*/ Associate Director* Clinical Operations Capabilities works collaboratively with cross-functional teams to ensure successful project outcomes and provides operative support to end-users.
Your Main Responsibilities are:
- Support development of / Co-develop and maintain Clinical Operations capabilities
- Define and implement of the strategic objectives and roadmap of Global Clinical Development Operations capabilities
- (Support) Identification of key stakeholders and establish relationships to align with their needs and expectations
- Manage and alter capability definitions to ensure the capability meets industry standards and compliance requirements
- Optimize Global Clinical Development Operations processes
- Identify gaps and further areas of improvement
- Develop and implement process improvements to enhance efficiency, reduce errors and increase compliance
- Act on process improvements to reach compliance with regulatory standards
- Manage Global Clinical Development Operations technology capabilities
- (Support) Co-Evaluation and co-implementation of technological solutions to support Clinical trial conduct, such as CTMS, SSU and Analytics (non exhaustive list)
- Collaborate with internal / external stakeholders to make sure Ensure the technology meets the organization's needs and integrates with other systems
- Support managing / Manage relationships with internal and external stakeholders
- Project Management in the GCP environment
- Collaboratively or individually, plan and execute capability-related projects to deliver business value
- Joint-work with cross-functional teams to ensure successful project outcomes
- Monitor project progress and manage deliverables, risks and issues
- Operational control and support
- Act as quality gate and control for data entry for clinical systems such as CTMS, SSU, etc.
- Act as a contact person for portfolio/project leads and cross-functional teams
- Provide operative support to end-users
- Continuous Improvement
- Stay informed about industry trends and emerging technologies
- Proactively seek opportunities for process improvement and innovation within the organization
- Commit to ongoing personal and professional development, to continuously learn and improve skills
What you have to offer:
-
Bachelor’s degree or higher in natural / life sciences
- Ready to take over / Responsible for recognizing problems and providing solutions
- Strong understanding of clinical trial operations, regulations, and compliance requirements
- Ability to work independently and in a team environment
- Ability to work in international cross-functional project environments
- Excellent communication and interpersonal skills, with the ability to collaborate with diverse stakeholders
- Ability to work in a fast-paced and dynamic environment
- Analytical mindset and attention to detail to ensure accurate and reliable data management
- Adaptability to learn new systems and technologies quickly
- Ability to identify and drive process improvement initiatives
- Strong organizational and time management abilities
- Proficiency in database management and Microsoft Office suite
- Knowledge of the Veeva Clinical Suite is an asset
- Excellent English (written and spoken), German optional
Benefits for you
We offer a competitive compensation package which will be determined by the contract type and selected candidate’s qualifications and experience.
How to apply
Apply now and simply send 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 by using our online form.
Please note:
- Only applications sent via our online form shall be considered.
- Only Candidates with the right qualifications and relevant experience shall be shortlisted
- Incomplete applications shall be rejected
- BioNTech will run a background check during the hiring process
We are looking forward receiving your application.
*BioNTech does not differentiate on the basis of gender, political opinion, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other aspect of personal status. We are committed to creating a diverse and inclusive environment and are proud to be an equal opportunity employer. Most important – it’s a match!
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