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Associate Director Translational Early Program

Bristol Myers Squibb

This is a Full-time position in Fort Worth, TX posted August 6, 2021.

Job Description At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science.

In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change.

We bring a human touch to every treatment we pioneer.

Join us and make a difference.

Translational Development at Bristol Myers-Squibb Bristol Myers Squibb is a leading global biopharma company focused on discovering, developing and delivering innovative medicines for patients with serious diseases.

We are focused on helping millions of patients around the world in disease areas such as oncology, hematology, immunology, cardiovascular and fibrosis.

Join us and make a difference.

We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development.

Through a culture of inclusion, we create a better, more productive work environment.

We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Summary/Scope Reporting to the VP, Translational Early Development, the Translational Early Program Lead will be part of the Immunology, Cardiovascular, and Fibrosis (ICF) Thematic Research Center (TRC) based in South San Francisco, CA.

Working in a cross functional team, the individual will be responsible for the development of the clinical biomarker strategy and precision medicine approach for early-stage drug development programs in cardiovascular and fibrotic diseases.

This individual will also have matrixed responsibilities to guide research programs within the translational research laboratories.

In addition, the individual will act as the translational development representative in early development teams and assume primary responsibilities, such as interacting with CROs and academic thought leaders to support contracting, sample analysis, and data delivery and interpretation of biomarkers in clinical studies.

The successful candidate will have prior experience interacting with project teams, clinical research physicians, statisticians, computational biologists, contract research organizations, academic collaborators, to deliver translational science that accelerates the development of medicines for patients in need.

Responsibilities will include, but are not limited to, the following: Responsible for managing the timelines and activities associated with clinical biomarker data delivery such as biomarker and assay selection, contracting (with support from an operations group), sample analysis, interpretation, and report generation, as well as involvement in trial-specific biomarker deliverables (e.g.

biomarker plans, protocol development, study reports) Work with internal translational research groups or CROs to develop and validate and selected biomarker assays for clinical implementation Implements innovative translational activities in early clinical studies through direct interaction with clinical research physicians, statisticians, clinical operations, computational biologists, contract research organizations, academic experts, and internal translational scientists Acts as a liaison between scientific and clinical project representatives to bridge the gap between discovery/translational research and clinical early development and enable back-translation from clinical studies to bench scientists Aid in biomarker data delivery for clinical studies through working with relevant functions and CROs; supports development of SOWs and interfacing with CRO for execution of services Participates in evaluation of CROs for data analysis and delivery capabilities, as needed Identify and collaborate in disease or therapeutic area-specific academic/industry partnerships and consortia, with the goal of advancing scientific understanding of disease pathophysiology to enable early target and biomarker identification and validation and generation of patient stratification hypotheses Interprets data and makes recommendations to enable decision-making Prepares and delivers internal and external presentations Supports regulatory submissions and regulatory interactions as needed Skills/Knowledge Required Understanding of drug discovery and development, especially transition from preclinical to clinical stages of development Experience in activities required for and related to clinical trial initiation, maintenance, and completion Experience in global regulatory interactions Experience in interacting with CROs and KOLs to manage projects and timelines Proven scientific/leadership expertise (working in teams, mentoring people, managing projects) Experience in mining of large datasets, either independently or in collaboration with bioinformaticians to understand disease pathophysiology and/or establish patient segmentation hypotheses Excellent record of performance and scientific accomplishments as demonstrated by impactful contributions to the scientific community, pipeline contributions, peer reviewed publications and patent applications highly desired Accountable for timelines and deliverables Prioritizes risks and implements contingency plans Communicates regularly; prepares and delivers presentations within the department, to governance and senior leadership bodies, and externally Recognizes cross-functional issues and communicates within the larger organization.

Provides expert guidance to multi-disciplinary teams and senior management.

Has a track record of delivering results, driving continuous improvements, and building effective cross-functional networks.

Ability to prioritize and manage time efficiently Strong verbal and written communication skills Accurate and detailed record keeping Excellent organizational skills

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