Sr. Scientist, Biomarker Operations Project Management

** Job Description
** The Senior Scientist, Biomarker Operations is responsible for the hands-on execution of outsourced biomarker data generation projects within the clinical portfolio. This role ensures operational excellence, data quality, and compliance throughout the lifecycle of biomarker assay projects. The Senior Scientist collaborates closely with cross-functional teams to deliver high-quality biomarker data for clinical trials and translational research.
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* Key Responsibilities:

**** Project Execution:
*** Plan, coordinate, and oversee outsourced biomarker data generation projects (e.g., omics assays) from initiation through data delivery.
* Track project deliverables, timelines, and resources
* Identify risks, proactively resolve issues, and maintain compliance at every stage of the process.
** Technical Support:
*** Apply expertise in biomarker assay technologies to support assay selection, platform evaluation, and troubleshooting.
* Stay current with internal and external trends, risks, and opportunities.
** Operational Excellence:
*** Implement and maintain streamlined workflows to maximize efficiency and data quality.
* Accurately track project information and maintain effective verbal and written communication internally and externally.
* Identify and resolve conflicting stakeholder needs.
* Contribute to a culture of continuous improvement and operational excellence.
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* Collaboration:

*** Work closely with other operational/scientific colleagues to support a cohesive and agile unit.
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* Qualifications:

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* Education:

*** Bachelor’s (with 5 years), Master’s or higher (with 3 years) in a scientific or technological field of study and relevant experience
** Required

Experience and Skills:

*** Demonstrated success in outsourced biomarker assay data generation
* Strong project management skills, with a track record of delivering high-quality data efficiently and compliantly
** Preferred

Experience and Skills:

*** Experience in drug discovery or clinical research
* Experience operating in a collaborative, matrixed, and fast-paced environment#EligibleforERP
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* Required Skills:

** Adaptability, Adaptability, Assay Development, Cell-Based Assays, Clinical Research, Clinical Study Management, Clinical Trial Planning, Clinical Trials, Data Analysis, Drug Discovery Process, Ethical Compliance, Ethical Standards, ICH GCP Guidelines, Medical Writing, Multiple Therapeutic Areas, New Technology Integration, Operational Excellence, Operational Performance Management (PM), Patient Care, Project Management, Protocol Development, Regulatory Submissions, Scientific Publications, Systems Troubleshooting, Therapeutic Knowledge {+ 1 more}
** Preferred

Skills:

** Current Employees apply

Current Contingent Workers apply
** US and Puerto Rico Residents Only:
** Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please  if you need an accommodation during the application or hiring process.

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** U.S. Hybrid Work Model
** Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of…