Upgrade your career in
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.
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.
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.
2. Lifetime LMS Access
- 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.
3. Blockchain-Based Certificates via CredSure
- CLINIVERSITY issues globally verifiable, tamper-proof credentials using blockchain technology adding authenticity and long-term value to your certification.
4. 100% Placement Support with Real-World Projects
- 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
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
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
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
Omkar C
Medical Writer
Sushree S
Safety Associate
Content to Bookmark
Insights and Trends in Clinical Research: Expert Articles and Updates.
Good Clinical Practice (GCP): Ethical and High-Quality Clinical Research
Good Clinical Practice (GCP) represents an internationally accepted set of
Best Practices for Data Accuracy and Regulatory Compliance in Clinical Data Management
In today’s fast-paced healthcare and pharmaceutical industry, Clinical Data Management
Regulatory Affairs: Building a Future-Proof Career in Pharma & Clinical Research
Before a new medicine reaches our hands, it passes through
From Campus to Corporate: How Certification Programs Make You Job-Ready
From Campus to Corporate: How Certification Programs Make You Job-Ready