Medical Intelligence Analyst

CryptoMize; India; On-site; INR 600,000 - 900,000; Full time

Job summary

CryptoMize in New Delhi is seeking a Medical Intelligence Analyst to join our headquarters on a full-time basis. You will monitor the clinical evidence base, track regulatory movements, and conduct literature surveillance to support healthcare-sector engagements with clients.

The role requires expertise in clinical literature retrieval, epidemiological reasoning, and translating medical statistics for decision-making.

Qualifications

• Clinical literature retrieval required and documented search strategies.
• Regulatory and pharmacovigilance concepts should be understood.
• Epidemiological reasoning and medical statistics translation skills.

Responsibilities

• Track the clinical evidence base behind healthcare accounts and brief the desk on changes.
• Read regulatory movement and convert insights into engagement calendars and actions.
• Run literature surveillance with documented search strategies and explicit inclusion criteria.

Skills

Clinical literature retrieval

Trial-design literacy

Regulatory-pathway reading

Pharmacovigilance awareness

Epidemiological reasoning

Medical statistics translation

Tools

PostgreSQL

Python

Metabase

Grafana

Git

Job description

Medical Intelligence Analyst jobs in Delhi at CryptoMize are open on a rolling, always-hiring basis — we staff sectoral-analytical capacity ahead of healthcare-sector engagements, not after they land. This is a full-time, permanent position with immediate joining, based at our New Delhi HQ, supporting healthcare-sector engagements with clinical and regulatory corpora. Below is the complete job description: the responsibilities you will own from day one, the requirements, the seniority path, and the selection process. Credentialed clinical and life-sciences analysts who want their sectoral measurement to mean something — intelligence reads that moved real healthcare decisions, dashboards that defended real client questions — should read to the end.

What you will actually do:

• Track the clinical evidence base behind every healthcare account — trial readouts, conference abstracts, pipeline changes — and brief the desk on what changed and why it matters
• Read regulatory movement the way strategists read polls: filing queues, inspection outcomes, drafting-committee shifts, and consultation windows converted into engagement calendars
• Run literature surveillance with medical-librarian rigor — search strategies documented, inclusion criteria explicit, citation chains followed back to primary publications

Skills that matter:

Clinical literature retrieval, Trial-design literacy, Regulatory-pathway reading, Pharmacovigilance awareness, Epidemiological reasoning, Medical statistics translation.

Tools you will use:

PostgreSQL 15, Python 3.11, Metabase & Grafana, Git-based analysis repos with review discipline.

Location:

New Delhi (HQ), E4, Vasant Vihar.

Type:

full-time permanent.

Availability:

immediate, rolling intake.

Compensation:

discussed at screening.