The objective of " The Beginners Course for Clinical Research" is to provide essentials of Clinical Research for recent graduates as well as experienced professionals in science, medicine & allied disciplines who are looking into careers in clinical research.
This course is developed and structured in a manner considering the beginner-level knowledge required in view of industry expectations. In this course, you’ll learn the principles and processes of clinical research, and basic clinical trial terminologies, and understand the different job roles of clinical research in developing new treatments and interventions.
Who Should Enroll?
1. Graduate or postgraduate degree in Pharmacy
2. Graduate or postgraduate degree in Medicine or any healthcare stream
3. Graduate or postgraduate degree in Life Sciences
4. Anyone from a related healthcare industry
What This Course Covers?
Module 1: Introduction & History Of Clinical Research
Module 2: Introduction To Preclinical Trial
Module 3: Clinical Trial Phases
o Phase 1
o Phase 2
o Phase 3
o Phase 4
Module 4: What is ICH-GCP
Module 5: Clinical Trial Stake Holders
o Investigator
o Sponsor
o CRO
o Regulatory Authority
Module 6: Informed Consent Process
Module 7: Introduction To Institutional Review Board / Institutional Ethics Committee
Module 8: Different Job Roles In Clinical Trials (CRA, CTA, CRC, CDA)
Module 9: Key Clinical Trial Terminologies
What Benefits/ Value Does This Course Offer?
Self Paced Learning with full explanation narrated for each module
Full lifetime access
Access on mobile and TV
Practice questions in all modules and a final assessment quiz
Certificate of completion
Content Developed By Industry People with 15+ years of experience
What are the job opportunities related to this course?
Below are a few job designations:
Clinical Research Co-ordinator (CRC)
Clinical Research Associate(CRA)
Clinical Trial Assistant (CTA)
Clinical Data Co-ordinator (CDC)
Clinical Research Data Specialist
Clinical Investigator or Clinical Researcher
Research Pharmacist
Clinical Project Manager
Medical/Scientific Writer
Clinical Trial Monitor
Pharmacovigilance Associate
Regulatory Affairs Associate
Centralized Monitor
Documentation Specialist
Trial Master File (TMF) Specialist
Clinical Trial Auditor