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The Research and Development team at Foundation Medicine is constantly pushing the envelope to transform cancer care.

Watch the video to see how each member has the chance to make a real impact. 

 

Scientist I, Data Management

  • Cambridge, Massachusetts, United States
  • Full Time

About the Job

The Data Management Scientist, Biometrics and Biomarkers is responsible for the oversight of data management activities and deliverables and providing the highest possible quality and efficiency of focused data management support to all life cycles for novel biomarker development and oncology companion diagnostic programs.

 

Key Responsibilities

• Perform query on database using SQL or other tools.

• Mitigate potential data management issues by reviewing protocols for cross-project consistency.

• Integrate data from multiple data sources for a given project, which may involve merging, reformatting of datasets and deriving new variables.

• Ensure the quality of data by identifying data errors or inconsistencies and work with appropriate personnel to resolve them.

• Perform data integration and transformation and deliver data tables based on data specifications.

• Manage current and historical data/results to build a knowledge base and ensure completeness and searchability.

• Ensure that all datasets, programs, and documentation are stored in appropriate locations under appropriate names for easy reference.

• Maintain high-level oversight on data quality metrics and DM deliverables.

• Perform ad-hoc data management and data analysis tasks.

• Collaborate with laboratory scientists, biostatisticians, technologists and regulatory affairs team on study design, planning, data preparation, programming, analysis and presentation of results.

• Other duties as assigned.

 

Qualifications

Basic Qualifications

• Master’s degree in bioinformatics, computer science, biostatistics, information systems or equivalent

• Fluency in one or several computing software for data programming

 

Preferred Qualifications

• 2+ years of relevant working experience (academic or industry)

• Experience in a programming role supporting clinical trial studies, biomarker studies in the biopharmaceutical/diagnostics/CRO industry

• Experience with Linux operating system

• Strong programming and computing skills; fluency in one or several scripting languages (Python, Perl), SQL and/or programming language (R, SAS)

• Knowledge and experience with Next-Generation Sequencing (NGS)

• Demonstrated ability of meeting project deadlines

• Demonstrated record of successful independent work and contributions to team projects

• Excellent communication, presentations and writing skills, and the ability to explain complex technical details in clear language

• Scientific understanding of cancer genetics and genomics

• Technical proficiency and creativity

• Strong interpersonal skills that include excellent skills in written communication, oral communication, collaboration, and problem solving with other departments and colleagues

• High level of detail orientation with a focus on quality

• Understanding of HIPAA and importance of privacy of patient data

• Commitment to FMI values: patients, innovation, collaboration, and passion

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