Job Description

Mainz, Germany; Cambridge, US | full time | Job ID: 9723





The Associate Director Clinical Data Management provides solid core and comprehensive data management expertise to provide high quality data management deliverables on clinical studies within his/her portfolio/platform program(s). He/She is responsible for leading the Clinical Data Management Teams and overlooking the execution of clinical trials, with regard to operational and administrative aspects. This includes day-to-day people management, resource planning, hiring and allocation of Data Management resources to the respective clinical portfolio/platform program(s). The ADCDM is working closely with the (Senior) Director Clinical Data Management to develop forward strategies and processes.

Key Responsibilities

Organizes and conducts team meetings. Takes care of team development, identification of high-performance team members and working on team development together with the (Senior) Director Clinical Data Management Provides guidance to project teams on the oversight and supervision of CRO/third party vendors and organizes trainings as needed. Acts as a mentor for new incomers or may delegate to appropriate team member this activity. Provides continuous feedback to develop team members. Contributes to the development and review of portfolio documents (includes contracts, guidelines, budgets, metrics, KPIs..) Complies with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents. Identifies the needs of new technology or tools for Data Management and takes active role during development and implementation. Supervises clinical data management activities within his/her portfolio/platform program and ensures it is per BioNTech standards and strategy. Escalates unresolved data or compliance issues to the functional manager(s). Provides guidance to Subject Matter Experts with regard to standard process developments Ensures the trials processes are aligned within his/her portfolio/platform program(s) and escalates any deviations or foreseen non-compliance. Provides expert support to the Clinical Development Team, on study design issues for BioNTech development projects and portfolio/platform program(s). Represents his portfolio/platform program(s) team among other department leads and functions, and supports cross-functional interactions and problem solving. Participates in strategic vendor selection processes for Clinical Data Management, and actively participate in vendor relationship management, includes escalation. Provides input on developing, revising, and maintaining core operating procedures and templates. Provides support or assist Quality assurance department in conducting audits involving data management activities

What you have to offer

Minimum qualifications: -


Natural/ life sciences or scientific background (university degree) or former experience in a CRO/ biotechnology/ pharmaceutical company in a Clinical Data Management position




Professional Experience: -


Minimum 12 years of experience in Clinical Data Management with wide practice in oversight of DM activities as a Lead and DM project management Profound knowledge of international guidelines (ICH-GCP) for the conduct of clinical research projects and experience with Clinical Database Systems and processes Experience with Clinical Database Systems and processes Experience in leading teams and resource planning




Skills and/or Knowledge: -


Very good English (written and spoken) Effective communicative skills, active listener Excellent organizational skills Able to motivate and lead a team/ used to work in a team Able to work under stressful conditions Ready to take over responsibilities Able to recognize problems and provide solutions Detail oriented Experience in usual software (Word, Excel, Power Point) Experience with at least one Clinical Data Management System (Medidata, OCRDC, Inform, …) Independent and pro-active way of working

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.

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