Senior Director

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Johnson & Johnson is recruiting for a Senior Director-Oncology Translational Research - Multiple Myeloma, located in Spring House, PA; Boston, MA; Raritan, NJ; Brisbane, CA or Remote (considered on a case by case basis). The Senior Scientific Director will serve within the Oncology Translational Research. The Oncology Translational Research group is responsible for all clinical biomarker and translational medicine strategies for compounds in development within the Oncology pipelines. In addition, the Translational Research group also covers disease biology for the indications of interest for the Oncology TA. The Senior Scientific Director will also be responsible for: Oversees and manages the translational strategy and implementation to support early and late development hematological malignancies programs in Oncology. Ensures the planning and execution of discovery and validation of predictive, prognostic, safety, and disease biomarkers Oversees the management of a Translational Research budget to support biomarker discovery and validation studies as well as supporting analysis of clinical samples Establishing and maintaining collaborative relationships with internal functional groups (e.g. Discovery, Clinical, CDTs), external academic research groups and CROS to facilitate the implementation of Translational Research strategies in Clinical trials. Leading collaborations and projects with external leaders in the hematological malignancies field Manages a team of staff including TR leaders a laboratory technicians Regular reporting of biomarker data to Oncology senior management. Responsibility for the biomarker sections in Clinical protocols, Investigator Brochures, Compound Development Plans generation of Clinical Study Report Managing the outstanding or in-house coordination of proposed analysis within clinical trials. Oversee data quality and ensure compliance and meeting projected timelines for project deliverables (e.g. protocol outlines, protocols, informed consent, strategy documents, analysis reports, etc.) Responsibility for resource planning for proposed projects.