Clinical Eligibility Reviewer — Oncology

Trials

Location: Bangalore / Hyderabad

Function: Clinical Data Review / Trial Eligibility Assessment

Company Description: RISA is dedicated to helping institutions succeed, beginning with leaders in oncology care. The organization focuses on designing an AI Operating System that aligns closely with real-world clinical and operational workflows. Through its BOSS Console, RISA supports oncology institutions in making more informed, efficient decisions. Team members collaborate at the intersection of medicine, technology, and operations to create practical, scalable solutions. The environment is mission-driven, innovative, and focused on impact within oncology and beyond.

About the Role

We're building a team of clinical eligibility reviewers to assess oncology trial patient records against protocol inclusion/exclusion criteria. This is a data-and-judgment role, not a field-based coordination position — there is no patient contact, no site visits, and no regulatory submission work involved.

You will review structured clinical data (EMR record ecords, lab results, medication histories, pathology reports) and determine whether a patient meets the eligibility bar for a given oncology trial, documenting your reasoning clearly enough to support audit and downstream model training.

This role sits closer to a clinical data reviewer or medical monitor than a traditional Clinical Research Coordinator (CRC). If you've worked in clinical monitoring, data review, or as a CRA and are looking for something less field-heavy but still clinically rigorous, this is built for that profile.

What You'll Do

Review EMR records, lab panels, medication/treatment histories, and pathology reports for individual patients

Apply oncology trial inclusion/exclusion criteria — staging, biomarker status, prior lines of therapy, organ function thresholds, comorbidities, washout periods, and more





Produce a clear eligibility verdict (eligible / not eligible / insufficient data) with documented, criterion-by-criterion rationale

Flag ambiguous or borderline cases for escalation rather than guessing

Maintain consistent, auditable documentation of your reasoning — not just your conclusion

Education:

MBBS or equivalent — strongest signal for clinical data interpretation

BSc Nursing or BPharm with clinical research experience

MSc in Clinical Research, Life Sciences, or Pharmacology

MPH with a clinical trials focus

Experience:

Minimum 2 years in clinical research.

CRO experience in clinical monitoring, data review, or as a CRA is strongly preferred

Oncology-specific trial experience (solid tumors, hematologic malignancies, or lung/breast/GI cancer) is ideal

Prior experience screening patients against protocol eligibility criteria, even in a support capacity

Experience reviewing medical records or structured patient data in any form

Strong plus, not mandatory:

CCRP, CCRA, or equivalent certification (ACRP India chapter, SOCRA)

ICH-GCP certification (expected baseline for anyone in this role)

Familiarity with oncology staging and biomarker frameworks — TNM staging, ECOG

performance status, biomarker-gated protocols, line-of-therapy tracking

Core Skills

Non-negotiable:

Protocol comprehension — able to read a dense eligibility criterion and apply it precisely, without over- or under-interpreting

Fluency in medical and oncology terminology: staging, treatment lines, lab value thresholds, drug classes, response criteria

High attention to detail — a false positive costs site time and erodes clinical trust

Robust English reading fluency, as all protocol documents and patient data are in English

Comfort working from structured data interfaces — lab values, medication lists ,diagnosis ,codes, pathology reports

Pay: ₹400,000.00 - ₹700,000.00 per hour

Work Location: In person

📌 Clinical Trails - Oncology (India)
🏢 Risa Labs
📍 India