Director CTSM IMPM

Director CTSM IMPM

Shape the Future of Clinical Trial Supply Management. Lead global strategies for Investigational Medicinal Product Management across Phase IIII clinical trials. Influence how life-changing therapies reach patients worldwide. Define and lead initiatives of all Clinical Trial Supply Management IMPM-Platform activities in global Phase I-III clinical trials (R&D Programs).

Key Responsibilities :

• Define and lead initiatives for CTSM platform activities, ensuring alignment with organizational goals and clinical trial requirements.
• Develop and implement performance objectives for the IMPM function, driving operational excellence and innovation.
• Design and structure initiatives based on platform portfolio strategies.
• Translate platform portfolio strategies into trial requirements and ensure adherence across all related clinical trials.
• Design distribution, manufacturing, and supply planning strategies for platform portfolios.
• Manage performance management for the IMPM function, ensuring continuous improvement and alignment with organizational goals.
• Define and lead implementation of process initiatives for the IMPM function.
• Provide CTSM feasibility perspectives to platform / portfolio core teams.
• Ensure platform portfolio requirements are followed in trials and oversee execution of assigned clinical portfolios.
• Liaise with internal and external stakeholders to address escalations and identify cross-functional initiatives or new ways of working.
• Lead and mentor individuals with diverse professional backgrounds and expertise, fostering a culture of openness, collaboration, and trust.
• Ensure compliance with GCP and GMP principles, as well as Quality Management Systems.
• Coordinate and compile regulatory documents, ensuring accuracy and consistency.
• Ensure function-specific SOPs are followed and implemented effectively.
• Build and maintain strong relationships with internal and external stakeholders.

What You Have to Offer :

Join a team that values agility, creativity, and accountability. Together, we deliver therapies that transform lives and set new standards in clinical trial supply management.

Expected Pay Range (US) : $168,100 / year to $268,700 / year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities.

We want to improve healthcare by making our innovations accessible worldwide. Therefore, we developed the first modular mRNA-manufacturing facilities based on a container solution called "BioNTainers". Help us build a regional manufacturing network in Africa & Australia : With the region and for the region. As a part of the local team, driving the establishment of the regional end-to-end mRNA manufacturing solutions.

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.

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.

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.