Clinical Literature Curator

NeoGenomics Laboratories

4d•Remote

About The Position

The Clinical Literature Curator supports NeoGenomics' scientific and medical intelligence programs by identifying, evaluating, and synthesizing scientific literature, clinical trial data, and other publicly available information related to oncology biomarkers and therapies. The role turns complex scientific evidence into clear, actionable insights for medical and scientific decision-making and helps maintain current, evidence-based knowledge of oncology biomarkers and their clinical utility. This is a remote position with a Monday–Friday shift.

Requirements

PhD in molecular biology, structural biology, biophysics, protein science, biochemistry, or a related discipline.
Demonstrated proficiency in data management, preparation of summary statements, and competitive intelligence deliverables.
Understanding of the hallmarks of cancer, targeted therapies and their molecular function, and oncology clinical trials.
Ability to read, understand, and critically evaluate scientific publications and synthesize information to communicate findings clearly to medical and scientific audiences.
General computer skills and ability to quickly learn and master computer programs, databases, and scientific applications.
Understanding of the value of supporting statements with appropriate citations and familiarity with citation formats and resources such as Google Scholar and EndNote.
Excellent writing, communication, and organizational skills.
Strong analytical skills and keen attention to detail.

Nice To Haves

At least one year of directly relevant experience in molecular biology, oncology literature research, clinical trials, therapeutics, and/or biomarkers.

Responsibilities

Conduct ongoing literature reviews to identify new research, cancer therapies, clinical trials, emerging procedures, and competitive intelligence relevant to oncology biomarkers.
Support the development, implementation, maintenance, and continuous improvement of databases and information systems used to curate and manage scientific and medical intelligence data.
Review, interpret, evaluate, synthesize, and summarize scientific literature and publicly available sources, including PubMed, ClinicalTrials.gov, and FDA publications, into accurate and concise clinical insights in accordance with SOPs.
Prepare written summaries, reports, and scientific content to support assessment of the clinical impact, utility, and actionability of oncology biomarkers.
Present evidence-based findings and recommendations to medical and scientific stakeholders, facilitating alignment on clinical relevance, impact, and actionability.