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      • Post Graduate Diploma in Drug Safety and Pharmacovigilance
      • Clinical Trial Management
      • Advanced Clinical Research
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Sollers CollegeSollers College
  • Contact Us
  • Courses
      Life Sciences
      Short term programs
      • Drug Safety Medical Narrative Writing
      • Drug Safety Aggregate Reporting
      • Drug Safety Signal Detection
      Certificate programs
      • Advanced Drug Safety and Pharmacovigilance
      • Drug Safety and Pharmacovigilance
      • Post Graduate Diploma in Drug Safety and Pharmacovigilance
      • Clinical Trial Management
      • Advanced Clinical Research
  • Sollers
    • About Us
    • Career Services
  • Blog

Advanced Clinical Research

Learn to conduct clinical research, collaborate with clinical scientists and enhance your skills in patient-oriented research.

 

Overview

Why Clinical Trial Management

This course provides training for students to learn how the Clinical Trial Management process works, developing complete Regulatory activities involved in Creating Documents and in Planning, Organizing, Monitoring, Recording, Analysis and Reporting of Clinical Trials. The program provides additional opportunities to learn about recent advancements as well as specializations in Risk-based Monitoring concepts.

In This Course

Study Startup: Understand the phases of the Clinical Trial, ICH-GCP guidelines, Study Feasibility, and Site Selection. Study Conduct: Learn about Site Monitoring Visits, which include Remote and Central Risk-Based Monitoring. Study Closeout: Learn about Site Close-Out Visit including both On-Site and Remote activities.

The Sollers Advantage

Work on real-time Case Scenarios, Clinical Tasks, and other Site Management activities taught by industry experts.

Learning Outcomes

  • Understand and implement Site selection, Site initiation, Site monitoring, and various other Site activities Activities
  • Students will assign sites, Site staff, IRB, and labs to the Pre-designed studies in the CTMS as a CRA
  • Students work on various Documents related to Site Visits as per the regulatory bodies requirement
  • Students will work on the Site binder and trial binder in the eTMF System
  • Students will be working with documentation related to local and central IRB (Regulatory board)

Highlights

For Hands-on Training in Aggregate Reporting:

We are enhancing our Argus Internship Sessions by incorporating hands-on training in Aggregate Reporting and believe that the knowledge and training that the students gain will enhance the scope for better opportunities in the drug safety and PV industry.

There will be 4 to 5 sessions of hands-on Aggregate Reporting training conducted on Saturdays from 10 am to 2 pm EST. The number of students per session will be limited and the number of students will be determined on a First Come, First Serve basis, strictly.

Course Duration

15 weeks (20+ hours each week)

3 Sessions /week

Engagement

150 hours

Get In Touch:

admissions@sollers.edu

or

Call Us Via:

73280 67846

Become a Certified
Clinical Trials Manager
Fast-track Your Life Sciences Career

100% Online | Industry-Driven Curriculum | Career Support Included

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Industry-focused training in Life Sciences with hands-on learning and career-ready skills.

Add: 90 Washington Valley Rd Bedminster, NJ 07921, USA
Admission: (732) 806 7846
Student Service: (848) 227 1023
Email: admissions@sollers.edu

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