Sr Director, Global Translational Sciences Lead, Molecular Imaging

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Sr Director, Global Translational Sciences Lead, Molecular Imaging

The Senior Director, Global Translational Sciences Lead, Molecular Imaging is responsible for driving the development of translational and biomarker objectives for preclinical and early clinical strategies in support of Bayer Radiology Nuclear Medicine diagnostic radiotracer assets. In this role, you will focus on innovating and adding value to patients by differentiating radiopharmaceuticals for use as targeted diagnostics and/or therapeutics and driving translational understanding of clinical trial data.

The primary responsibilities of this role, Senior Director, Global Translational Sciences Lead Molecular Imaging, are to:

• Ensure effective collaborations between preclinical research and clinical development, establishing strong target-to-disease connections for radiotracers as standalone diagnostics or in co-development with targeted radio therapies (TRTs) or other therapeutics;
• Integrate and validate technical knowledge of radiopharmaceuticals’ mechanisms of action and identification of imaging biomarkers in preclinical development into strategies for the clinical development of diagnostic assets;
• Develop the overall early clinical development strategy of radiotracer assets in co-creation with relevant thought-leader communities, vendors, and partners with a central customer/patient value approach;
• Develop and oversee clinical trial designs (First in Human to Phase 2a) for radiotracer assets, in collaboration with vendors and partners;
• Lead the matrix-management of clinical trial teams, collaborating across the organization and externally with service providers/investigator sites;
• Lead all aspects of translational studies and deliverables with CROs and collaborators to support new and ongoing clinical studies;
• Provide technical expertise as required for the development, troubleshooting, and tech transfer of manufacturing methods to external vendors/partners;
• Support the development of cGLP and cGMP radiopharmaceutical manufacturing processes to enable clinical development activities;
• Review experimental data both internally and from external vendors/partners, analyze, summarize, and interpret results, and relay findings to stakeholders, internal and external (including representing Bayer at regulatory meetings) through summary reports, technical documents, or presentations;
• Author/co-author pre-clinical and clinical documents as applicable, such as IBs, protocols, study reports, statistical analysis plans, publications, and regulatory submissions;
• Support optimization of standard methodologies in clinical trial operations and adopt an open learning and sharing environment, optimizing methodologies and utilizing digital tools in clinical trials;
• May support and contribute to Business Development & Licensing (BD&L) activities;
• Mentor colleagues and promote knowledge-sharing.
• The primary location for this role is Whippany, NJ. Residence-based candidates located in the US and willing to travel may also be considered for this role.

Bayer seeks an incumbent who possesses the following:

• Minimum of a Master's Degree, MD, Pharm
  
  D, or PhD in Molecular Imaging/Nuclear Medicine or a related field;
• At least 10 years of experience in the Pharma Industry, with 5 or more years in Translational Science/Medicine and/or Early Clinical Development (Phase 1-2a) of Radiopharmaceuticals, preferably in diagnostic radiotracers;
• A track record of clinical trial management/operations of Radiopharmaceuticals and broad knowledge of the…