Oncology Program Leader SourceMDx
THIS JOB HAS EXPIRED Education Level: Minimum Doctorate Degree in Molecular Biology or related field.
Experience: Minimum 5+ years in a pharmaceutical/clinical setting with a broad-based exposure to oncology trials, therapeutics and diagnostics.
Demonstrated background in all phases of cancer drug development from preclinical
to clinical, complemented with a strong fluency in cancer therapeutics and
related biological pathways.
Ability to understand and translate RNA transcript-based gene expression results
in the context of biology and medicine.
Strong advocate of the application of transcription profiling across the drug
Ability to work with interdisciplinary teams within pharmaceutical and
biopharmaceutical organizations to support translational biomarker programs for
Broad-based knowledge of cancer and inflammation, particularly causal links and
common underlying mechanisms.
Strong background in RNA transcript measurement and platforms.
Excellent organizational, interpersonal and written/oral communication skills.
Understanding of general statistical methods with the ability to learn more
advanced statistical concepts.
Computer skills must include Microsoft Word, Microsoft Excel and Power Point
Manage multiple clinical projects and associated activities within a
comprehensive oncology program involving Source MDx, high profile academic
collaborators and pharmaceutical/biopharmaceutical clients.
Generate program related documents (project meeting summaries and updates,
interim and final data analysis reports and presentations) for academic
collaborators, pharmaceutical/biopharmaceutical clients and internal use (Source
MDx management, Scientific Advisory Board and Board of Directors).
Serve as an industry advocate of RNA-transcript-based molecular diagnostics in
oncology by actively contributing towards the publication of study results in
leading journals and the presentation of findings in highly regarded scientific and
business forums (conferences, specialized meetings etc.)
Understand the emerging regulatory landscape of approval and commercialization
of molecular diagnostic assays.
||Boulder, CO |
THIS JOB HAS EXPIRED