D2C Beginners Blueprint (Diploma in Clinical research and Pharmacovigilance)
About this course
This course is about understanding the concept of clinical research and pharmacovigilance through which you will be able to get your dream job inside pharmaceutical industry in just 2 months.
You will learn how any drug is being discovered and how clinical trials happens…What are the different phases of any clinical trials and different kinds of approvals required to bring any drug into market…After successful completion of any clinical trial how any drug undergoes the phase of post marketing surveillance which we call as pharmacovigilance… What and how pharmacovigilance is conducted and what’s the impact of pharmacovigilance.
Benefits of taking this course:
1) Crisp and clear, job-oriented program
2) Unlimited Live Q and A session every weekend
3) Opportunity to learn from real industry experts
4) Instant resolution of query with turn around time of 24 hrs
5) Authentic and no false promises
6) 100 % Job assistance
7) Job assistance till the time you get the job (not limited to two months)
Click on below link to know what our student speaks about us:
https://g.page/r/CWxF7qZXiPAPEAg/review
You will be eligible for below job roles after this course:
1) Clinical research coordinator
2) Clinical trial coordinator
3) Medical writing trainee
4) Medical writing associate
5) Clinical data management trainee
6) Clinical data management associate
7) Safety associate trainee
8) Pharmacovigilance associate
9) Pharmacovigilance executive
10) Pharmacovigilance officer
By signing up for this course, you will have the opportunity to meet Dr. Neema Bisht , Founder and Director Careerinpharma
Syllabus
Module 1 Clinical trial and phases
Module 2 Introduction to pharmacovigilance
Module 3 Adverse drug reaction, adverse event and serious adverse event
Module 4 ICH GCP (International conference on harmonization and good clinical practices)
Module 5 Institutional review board/Ethics committee
Module 6 Informed consent
Module 7 Dechallenge, rechallenge and causality assessment
Module 8 Confidentiality and privacy in clinical trial
Module 9 Signal detection and risk management plan
Module10 Quality assurance and research protocol
Module 11 Research protocol(continued) and type of reports in pharmacovigilance
Module 12 Documentation and record keeping
Module 13 Case processing in pharmacovigilance
Module 14 Roles and responsibilities. Recruitment and retention in clinical trial
About the instructors
Dr. Neema Bisht
Founder and Director, Careerinpharma
Dr. Manjula R
Senior pharmacovigilance expert
Bhawna Rawat
Query expert