Translational Oncology Scientist, Clinical Reporting

Foundation Medicine, Inc.; Morrisville (NC); Hybrid; USD 114,000 - 143,000; Full time

Job summary

Foundation Medicine, Inc. in Boston, MA, seeks a Scientist I, Translational Oncology and Clinical Reporting to support personalized diagnostic reports through literature research, scientific analysis, and writing. You will work with Medical and Clinical Research teams to ensure concise, physician-focused content.

This regulated role requires collaboration across departments, development of new guidance from literature, and timely delivery while upholding patient data privacy standards.

Qualifications

• Ph.D., M.D., or equivalent in cancer biology or related field; OR
• MS with 7+ years of relevant work experience; OR
• BS with 10+ years of relevant work experience

Responsibilities

• Identify, interpret, synthesize and summarize literature and sources relevant to Foundation Medicine's cancer genomic test.
• Collaborate with internal and external scientists and physicians to review and extend medical content.
• Generate new clinically-focused content based on literature and guidelines.
• Contribute to development and maintenance of Foundation Medicine's clinical oncology knowledgebase.
• Support additional research projects within TOCR and across departments.
• Communicate with stakeholders about patient genomics.
• Deliver on tight deadlines.
• Comply with FMI's attendance policies.

Education

Ph.D., M.D., or equivalent in cancer biology, cell biology, genetics, biochemistry, molecular biology, molecular oncology, translational medicine or similar field

MS with 7+ years of relevant work experience

BS with 10+ years of relevant work experience

Job description

Foundation Medicine, Inc. in Boston, MA, seeks a Scientist I, Translational Oncology and Clinical Reporting to support personalized diagnostic reports through literature research, scientific analysis, and writing. You will work with Medical and Clinical Research teams to ensure concise, physician-focused content.

This regulated role requires collaboration across departments, development of new guidance from literature, and timely delivery while upholding patient data privacy standards.