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Clinical Research Data Management Pharmacovigilance Medical Writing Medical Coding Medical Scribing

Enroll in our expert-led courses to gain essential skills and knowledge in clinical trials, data management, and regulatory compliance.

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Aditi
Ashwini D
Chaitanya B
Devkanya k
Gunjan A
Gunjan Amle
Hanumant S
Kavery J
Mangesh S
Mayur J
Nandini B
Nireeksha R
Onkar D
Parul Singh
Priyanka S
Rakshita
Rakshitha
Sarthak B
Shahin M
Shivani-S.-TCMS

Cliniversity offers practical, hands-on training with every course.

Gain real-world skills through online learning and expert-led sessions, preparing you for a successful career in Clinical Research and Medical Coding.

Certification in Clinical Research

Certification in Clinical Research

  • Online
  • Hands-On Training
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Advanced Diploma in Clinical Research

  • Online
  • Hands-On Training
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Medical Coding Course

Certification in Medical
Coding

  • Online
  • Hands-On Training
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Certification in Clinical Research + Medical Coding

  • Online
  • Hands-On Training
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Top Reasons to Join Cliniversity

This training enhances their ability to use pharmacovigilance tools and methodologies, crucial for maintaining compliance with regulatory standards and improving overall healthcare outcomes.

1. Hands-On Training on Pharmacovigilance Databases
  • Students gain practical exposure to real-world PV tools and safety databases, enhancing their job readiness from day one.
  • Cliniversity uses PVEDGE Pharmacovigilance Database to provide Pharmacovigilance Hands-on Training.
  • Get unlimited access to learning materials, recorded lectures, and course content anytime even after course completion.
  • LMS has extensive pre-recorded sessions for different module, help students in navigating details upon program completion.
  • CLINIVERSITY issues globally verifiable, tamper-proof credentials using blockchain technology adding authenticity and long-term value to your certification.
  • Benefit from career support, resume guidance, mock interviews, and placement opportunities with top CROs, pharma companies, and research organizations.

Join our comprehensive clinical research courses designed by industry experts

Enhance your skills, gain certification, and advance your career in clinical research. Enroll now for in-depth training and real-world applications.

Clinical Research

  • Clinical Research Coordinator
  • Clinical Research Associate
  • CTA

Data Management

  • Clinical Data Analyst
  • Clinical Data Associate
  • Clinical Data Manager

Pharmacovigilance

  • Case Processing Expert
  • Drug Safety Associate
  • Clinical Safety Scientist

Medical Writing

  • Copy Editor
  • Medical Content Writer
  • Scientific Writer

Medical Coding

  • Medical Coder
  • Clinical Doc specialist
  • Clinical Coder

Medical Scribing

  • Medical Biller
  • Claims Processor
  • Billing Specialist

Why Student Choose Us

Take The Next Step Toward Everlasting Clinical Research Industry

50 +

Recruiters

150 +

Expert Trainers

2000 +

Professional Network

5 LPA

Recent CTC

Choose Your Role

Gain the knowledge and skills you need to advance.

Clinical Research Coordinator (CRC)/ Study Coordinator

Coordinates clinical trial activities at research sites, ensuring protocol compliance and patient safety. Acts as a bridge between investigators, sponsors, and ethics committees.

  • Domain: Clinical Research
  • Assists in managing clinical trial operations at sites.
  • Handles patient recruitment, informed consent, and trial documentation.
  • Works closely with investigators and sponsors.
  • Employer Industry:
  • Clinical Trial Sites
  • Hospitals/Medical Colleges
  • Contract Research Organizations (CROs)
  • Site Management Organizations (SMOs)

Clinical Data Associate (CDA) / Data Analyst (Entry-Level)

Handles collection, cleaning, and validation of clinical trial data. Works with EDC tools to ensure data accuracy and regulatory compliance.

  • Domain: Clinical Data Management (CDM)
  • Responsible for data entry, data cleaning, and validation checks.
  • Works with EDC (Electronic Data Capture) tools like Medidata, Rave.
  • Ensures data accuracy and consistency for trials.
  • Employer Industry:
  • Contract Research Organizations (CROs)
  • Pharma & Biotech Companies
  • Clinical Data Management Service Providers

Drug Safety Associate (DSA)/ Case Processing Expert

Processes and evaluates adverse drug reaction reports (ICSRs). Ensures timely reporting to regulatory authorities using PV tools.

  • Domain: Pharmacovigilance
  • Handles case processing of adverse drug reactions (ICSRs).
  • Enters and codes medical data using MedDRA and WHO-DD.
  • Assists in narrative writing and report submission to regulatory bodies.
  • Employer Industry:
  • Pharmacovigilance Service Providers
  • CROs
  • Pharmaceutical Companies

Junior Medical Writer / Trainee Scientific Writer Coordinator

Creates clinical trial documents like protocols, reports, and summaries. Requires medical knowledge, strong writing skills, and familiarity with ICH-GCP.

  • Domain: Medical Writing
  • Assists in preparing clinical documents like protocols, CSRs, and safety summaries.
  • Edits and formats documents as per ICH-GCP and sponsor guidelines.
  • Requires strong written communication and medical knowledge.
  • Employer Industry:
  • CROs
  • Medical Communications Agencies
  • Pharma/Biotech Companies
  • Health Content Providers

Regulatory Affairs Associate (Trainee)

Assists in preparing and submitting regulatory documents for product approvals. Monitors global regulatory guidelines and supports compliance.

  • Domain: Regulatory Affairs
  • Supports dossier compilation and submission (eCTD, CTD formats).
  • Tracks regulatory updates and assists in responding to queries.
  • Coordinates with cross-functional teams for regulatory filings.
  • Employer Industry:
  • Pharma/Biotech Companies
  • CROs
  • Regulatory Consulting Firms
  • Medical Device Companies

Medical Scribe (Virtual / Onsite)

Documents real-time patient-physician interactions into electronic medical records. Improves doctor efficiency and accuracy in clinical documentation.

  • Domain: Medical Scribing
  • Works in real-time with US physicians to document patient encounters.
  • Prepares SOAP notes, prescriptions, and test orders during consultations.
  • Requires good listening, typing speed, and clinical terminology knowledge.
  • Employer Industry:
  • Medical Scribing Companies
  • US Healthcare Documentation Firms
  • Telemedicine & Health IT Companies

Our mission is to equip healthcare professionals with the essential skills and knowledge enter in dynamic field

Cliniversity offers programs via LIVE Online Instructor-Led, Self-Paced, and Classroom formats. The programs are industry-designed and include hands-on training on Pharmacovigilance software tools.

Hands on Training on
Pharmacovigilance Software

Cliniversity provides live hands-on training on PV Tool,
also provides an add on certification for the same.

Placement Support

Our Placement support team help you to reach your
dream career opportunities in leading CROs, Pharma and IT Companies.

Why students choose us to gain knowledge

Our expert-led clinical research courses and enhance your skills in clinical data management. Join now for comprehensive, industry-relevant training designed for career advancement in the healthcare and pharmaceutical sectors.

Medical Coding

Clinical Data Management

Clinical Research

Pharmacovigilance

Become a Certified Clinical Research Professional.

At Cliniversity, we pride ourselves on our outstanding placement record in the clinical research sector. Our students are highly sought after by top CROs and leading research institutions. With a robust training program and hands-on experience, our students are well-equipped to excel in roles such as Clinical Research Associates, Data Managers, and Pharmacovigilance Specialists. Join us and launch your career with confidence, knowing you have the skills and support to succeed in the dynamic field of clinical research!

Shivani Shukla

Data Entry Operator

Gunjan Amle

Research Coordinator

Aditi

Data Coordinator

Parul Singh

Research Coordinator

Sarthak B

Data Coordinator

Amatul V S

Drug Safety Associate

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Omkar C

Medical Writer

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Sushree S

Safety Associate

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Insights and Trends in Clinical Research: Expert Articles and Updates.

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