First 30 minutes always free

Talk to a Real Pharma Expert

Get 1:1 career guidance from industry veterans who've been exactly where you are. No generic advice — personalised, domain-specific mentoring.

01

Pick your domain expert

CDM, PV, Regulatory, SAS or Clinical Ops

02

Choose session length

30 min free, extend at ₹500/hr

03

Show up on Google Meet

Link sent to your email automatically

🗂️
CDM10+ years

CDM Expert

From Data Entry to Data Manager — your CDM career mapped out

Specialises in helping freshers break into Clinical Data Management. Covers CDASH, CDISC standards, edit checks, database design, and CCDM certification prep. Has placed students at top CROs including IQVIA and Parexel.

CDASH / CDISCMedidata RaveOracle InFormCCDM PrepCRF Design
Worked at: IQVIA, Novartis, J&J
4.9

Starting from

FREE / 30 min

🛡️
PV8+ years

PV Expert

Your guide to the world of Drug Safety & Pharmacovigilance

Deep expertise in adverse event reporting, signal detection, and regulatory submissions. Helps freshers understand ICH E2E guidelines, ICSR processing, and how to crack PV interviews at global pharma companies.

ICSR ProcessingSignal DetectionICH E2EArgus SafetyPSUR/PBRER
Worked at: Parexel, ICON, Syneos
4.9

Starting from

FREE / 30 min

📋
Regulatory9+ years

Regulatory Expert

Navigate drug approvals — your regulatory career accelerated

Experienced in global regulatory submissions across CDSCO (India), USFDA, and EMA. Guides freshers through CTD format, dossier preparation, and the art of building a regulatory portfolio from scratch.

CTD FormatCDSCO SubmissionsUSFDA eCTDDossier ReviewRegulatory Strategy
Worked at: Dr. Reddy's, Sun Pharma, Covance
4.9

Starting from

FREE / 30 min

💻
SAS7+ years

SAS Expert

From SAS basics to CDISC-ready datasets — crack the code

Specialises in clinical SAS programming for freshers — from base SAS fundamentals to SDTM and ADaM dataset creation. Helps students build their first real SAS portfolio and clear technical interviews at CROs.

Base SASSDTMADaMTLF GenerationSAS Certification
Worked at: Cognizant, Wipro Life Sciences, IQVIA
4.9

Starting from

FREE / 30 min

🔬
Clin Ops11+ years

Clinical Ops Expert

Site visits, monitors, and trials — your CRA career starts here

Veteran Clinical Research Associate who has monitored trials across India and Southeast Asia. Guides freshers on CRA interview preparation, Good Clinical Practice (GCP), site visit reports, and how to land their first CRA role.

GCP / ICH E6Site MonitoringCRA Interview PrepSDV/SDRRegulatory Submissions
Worked at: ICON, PRA Health Sciences, Veeva
4.9

Starting from

FREE / 30 min

Session Pricing

Transparent pricing. No hidden fees. First 30 minutes on us.

30 min
FREE
60 min
250
90 min
500
120 min
750
✦ Sessions are conducted on Google Meet. Calendar invite sent immediately after booking. Extensions (additional 30-min blocks at ₹250) can be arranged directly during the session.

Common Questions

Is the first 30 minutes truly free?

Yes, completely. No credit card required for the free 30-minute session. Just fill your details and pick a time slot.

Who are the experts?

All experts are verified pharma professionals with 7–12 years of experience at top CROs and pharma companies. We don't reveal names publicly to protect their privacy.

What if I need more than 30 minutes?

You can book a longer session upfront (60/90/120 min). Or if your free session runs long, you can arrange an extension directly with the expert during the call.

What platform is used for sessions?

All sessions are on Google Meet. A calendar invite with the Meet link is sent to your email immediately after booking.

Can I get a refund?

Yes — if the expert cancels or you cancel 24+ hours before, you get a full refund to your original payment method within 5-7 business days.

Which domains are covered?

CDM, Pharmacovigilance, Regulatory Affairs, SAS Programming, and Clinical Operations. More domains coming soon.

Not sure which domain to choose?

Book a free 30-minute session with our Generic expert — they'll help you map your background to the right pharma domain.

Explore 90-Day Roadmap