RISA has announced an opening for the position of Clinical Eligibility Reviewer – Oncology Trials. This opportunity is suitable for healthcare and life sciences professionals with experience in clinical research, clinical monitoring, medical record review, or clinical data review.

The RISA Clinical Reviewer job focuses on assessing patient clinical records against oncology clinical trial inclusion and exclusion criteria. Unlike a traditional Clinical Research Coordinator (CRC) position, this is primarily a clinical data review and trial eligibility assessment role, with no patient contact, site visits, or regulatory submission responsibilities.

Professionals with MBBS, BSc Nursing, BPharm, MSc Clinical Research, Life Sciences, Pharmacology, or MPH qualifications may be considered depending on their relevant clinical research experience.

RISA Clinical Reviewer Job Overview

About RISA

RISA develops technology solutions designed around real-world healthcare and oncology workflows. The organization works at the intersection of medicine, technology, clinical operations, and artificial intelligence.

For this position, RISA is building a team responsible for reviewing oncology patient records and determining whether patients satisfy specific clinical trial eligibility criteria.

What Does a Clinical Eligibility Reviewer Do?

A Clinical Eligibility Reviewer evaluates clinical information such as electronic medical records, laboratory results, pathology findings, diagnoses, medications, previous treatments, and other patient data.

The reviewer compares this information against the inclusion and exclusion criteria of an oncology clinical trial protocol and determines whether the available evidence supports trial eligibility.

The final assessment may classify a patient as:

• Eligible
• Not Eligible
• Insufficient Data

Reviewers must also provide clear criterion-by-criterion reasoning supporting their assessment.

Key Responsibilities

Selected candidates for the RISA Clinical Reviewer vacancy will be responsible for:

• Reviewing EMR records and structured patient clinical data.
• Evaluating laboratory panels and organ-function parameters.
• Reviewing medication and treatment histories.
• Interpreting pathology reports and relevant clinical findings.
• Applying oncology clinical trial inclusion and exclusion criteria accurately.
• Evaluating cancer staging and biomarker requirements.
• Reviewing previous lines of therapy and treatment history.
• Assessing washout periods and protocol-defined treatment restrictions.
• Reviewing comorbidities and laboratory thresholds.
• Determining whether patients are eligible, not eligible, or require additional information.
• Preparing clear criterion-by-criterion eligibility rationales.
• Escalating ambiguous or borderline cases rather than making unsupported assumptions.
• Maintaining consistent and auditable clinical review documentation.
• Supporting high-quality downstream clinical and AI/model-training workflows.

Educational Qualifications

RISA has mentioned several healthcare and life sciences qualifications for the Clinical Reviewer role.

Candidates may have:

MBBS or equivalent
Considered the strongest educational background for direct clinical data interpretation.

BSc Nursing
Candidates should have relevant clinical research experience.

BPharm
Pharmacy graduates with relevant clinical research experience may apply.

MSc Clinical Research

MSc Life Sciences

MSc Pharmacology

MPH
Preferably with a clinical trials focus.

Educational qualification alone may not be sufficient because the job description specifically asks for relevant clinical research experience.

Experience Required

Candidates should have a minimum of 2 years of clinical research experience.

RISA particularly prefers professionals with CRO experience involving:

• Clinical monitoring
• Clinical data review
• CRA responsibilities
• Medical record review
• Patient eligibility screening
• Protocol-based clinical assessment

Previous experience in oncology clinical trials involving solid tumors, hematological malignancies, lung cancer, breast cancer, gastrointestinal cancers, or related therapeutic areas would be particularly valuable.

Experience screening patients against clinical trial inclusion and exclusion criteria is also highly relevant.

Core Skills Required

Candidates should demonstrate strong clinical trial protocol comprehension and the ability to interpret complex eligibility criteria precisely.

Important skills include:

• Clinical trial protocol interpretation
• Inclusion/exclusion criteria assessment
• Medical terminology
• Oncology terminology
• Clinical data review
• Electronic medical record review
• Laboratory value interpretation
• Pathology report review
• Medication history assessment
• Oncology staging concepts
• Treatment line assessment
• Biomarker interpretation
• Strong English reading comprehension
• Attention to detail
• Clinical judgment
• Structured documentation
• Data-driven decision-making

Candidates must be comfortable working with structured clinical data interfaces containing laboratory values, diagnosis codes, medications, pathology findings, and treatment information.

Oncology Knowledge Preferred

Knowledge of the following concepts can strengthen a candidate’s profile:

TNM Staging: Understanding tumor, node, and metastasis classifications used to characterize cancer extent.

ECOG Performance Status: Familiarity with performance-status assessments commonly incorporated into oncology trial eligibility.

Biomarker-Gated Protocols: Ability to understand eligibility requirements based on molecular or pathological biomarkers.

Line-of-Therapy Tracking: Understanding previous cancer treatments and how prior therapies influence clinical trial eligibility.

Certifications That Can Add Value

The following certifications are advantageous but are not stated as mandatory:

• ICH-GCP certification
• CCRP certification
• CCRA certification
• ACRP-related clinical research certification
• SOCRA certification

ICH-GCP knowledge is particularly important for professionals working in clinical trials.

Who Should Apply?

This RISA Clinical Reviewer position may be particularly relevant for professionals currently working as:

• Clinical Research Associates
• Clinical Data Reviewers
• Clinical Trial Reviewers
• Clinical Research Professionals
• Oncology Clinical Research Professionals
• Medical Record Reviewers
• Clinical Monitoring Professionals

Candidates seeking to move away from field-heavy clinical research responsibilities while continuing to work closely with patient data and clinical trial protocols may find the position especially relevant.

Is This RISA Job for Freshers?

No. This vacancy is not primarily a fresher position.

The job description specifies a minimum of 2 years of clinical research experience. Candidates with experience in clinical monitoring, clinical data review, CRA activities, medical record assessment, or trial eligibility screening are more closely aligned with the requirements.

Benefits of This Opportunity

The original job posting does not specify a formal employee-benefits package. However, the professional scope of the position provides exposure to:

• Oncology clinical trials
• Clinical data interpretation
• Protocol eligibility assessment
• Structured patient data
• Medical record review
• Technology-enabled clinical workflows
• Auditable clinical decision-making
• AI-supported healthcare operations

Candidates should confirm compensation, insurance, leave, and other employment benefits directly with RISA during the recruitment process.

Expected Salary

RISA has not disclosed the salary in the provided job advertisement.

For structured-data purposes, an estimated market range of approximately ₹6,00,000 to ₹12,00,000 per year may be considered for comparable clinical research/data-review profiles in India, depending on qualification, oncology expertise, previous CRO experience, and overall clinical research background.

Important: This is an estimated market range and not an officially disclosed RISA salary. Candidates should confirm compensation directly with the employer.

How to Apply

Application Link