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OUR MENTORS. YOUR MOMENTUM.

Shaped by
expert hands.

Learn where clinical research happens. Be guided by the people who understand the work.

Your training combines practical involvement at a research site or hospital with online teaching and mentor guidance.

See how hybrid learning works ↓
ON THE GROUNDEXPERT GUIDANCE ONLINEOne connected learning experience.

01 / THIS IS HYBRID, THE FERAVENA WAY

On site. Online.
Always connected to practice.

Ground-level experience is the foundation.
Online teaching helps you understand and improve.

01 / YOUR TRAINING PLACEMENT

Research site
or hospital.

You’ll be placed at a research site or hospital for practical training, observing, assisting with and taking part in activities under site supervision.

  • See how the site works
  • Get involved in study activities
  • Build confidence through practice
IN PERSON · ON THE GROUND
02 / YOUR EXPERT GUIDANCE

Online teaching.
Real-world context.

Your mentors explain how to carry out each activity, why the steps matter and the regulations and responsibilities behind the work.

  • Learn the method and the reasoning
  • Discuss questions from site experience
  • Apply mentor feedback on the ground
ONLINE · MENTOR SUPPORTED

Experience → explanation → feedback → better practice.
What you encounter on site becomes part of your online learning. What you learn online comes back into your practice.

Placement here means a training placement. Your site team supervises involvement in study activities according to your training stage and the site’s requirements.

02 / WHO WILL GUIDE YOU

Different expertise.
Shared focus: your growth.

Operations. Data. Safety.
The roles supporting your practical learning.

CLINICAL OPERATIONS01

Senior Operations Manager

See how a research site comes together.

Guides your understanding of site start-up, study coordination, monitoring preparation and communication with the Ethics Committee.

Site readiness · Study workflows · Monitoring preparation
CLINICAL DATA02

Clinical Data Associates

Turn everyday observations into clear records.

Connect source narration with data entry, accuracy checks and query handling, helping you understand how site documentation supports clinical data quality.

Source documentation · Data entry · Query handling
PHARMACOVIGILANCE03

PV Associates

Learn the detail behind safety reporting.

Guide you through adverse-event documentation, safety information workflows and clear communication, with online explanations that connect back to site activities.

AE documentation · Safety workflows · Communication
PHARMACOVIGILANCE04

PV Manager

Understand the reasoning behind the process.

Brings the broader safety perspective to your learning: reporting responsibilities, escalation, quality review and the regulatory context behind each step.

Safety oversight · Escalation · Regulatory context

03 / HOW THE TWO PARTS WORK TOGETHER

One activity.
A complete learning loop.

For example: preparing for a monitoring visit.

  1. ON SITE

    Get involved.

    Assist the site team with organising study records and preparing for the visit.

  2. ONLINE

    Understand the why.

    Discuss the preparation steps, documentation expectations and relevant requirements with your mentor.

  3. BACK IN PRACTICE

    Put it to work.

    Use the feedback during your next supervised activity, with a clearer understanding of the process.

YOUR CAREER STARTS WITH INVOLVEMENT

Get closer
to the work.
And the experts.

Talk to us about hybrid training, research-site placement and the mentors who will guide your learning.

Explore all nine practical activities ↗

LET’S GET TO KNOW YOU

Make your move.

Request a callback from our team.

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Talk about hybrid training ↗