workflows like trial matching, registry curation, visit

prep, and quality reporting. We replace that manual work with task-driven AI agents that sit

inside the EMR and process records with >95% accuracy, at scale, in real time.

We have grown 10x in the last one year and are processing millions of documents monthly.

Roles & Responsibilities include the following:

● Clinical Trials Acumen: Interpret the Inclusion and Exclusion criteria outlined in the

clinical trials on clinicaltrials.gov and in study protocols, and use this information to

assess patient eligibility for clinical trials.

● Market Research and Competitive Intelligence: Ability to perform basic market research

and competitive intelligence, including gathering, organizing, and summarizing insights

from public sources, reports, and industry databases.

● Understanding of oncology, medical, and pathology terminologies.

● Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and

draw appropriate insights.

Must Have:

● Bachelor's or Master's degree in a relevant field such as Science, Biotechnology, or

Pharmaceutical Sciences

● Prior knowledge of clinical trials and clinical research is preferred

● Proficiency with G-Suite tools (Docs, Sheets, Drive, etc.)

● Fast learner with strong problem-solving skills

● Excellent written and verbal communication in English

Research Operations Intern