6-Week Career Accelerator Program
6-Week Career Accelerator Program
Clinical
Clinical
Research
Data
Accelerator
Accelerator
Program
Programme
6Weeks
40hours
1Project
6Weeks
6Weeks
6Weeks
40hours
1Project
6Weeks
6Weeks
6Weeks
40hours
1Project
6Weeks
6Weeks
A 6-week practical program built for life science graduates aiming to enter clinical research, with real-world exposure to monitoring visits, SDV, and CRO-level reporting standards.
About Program
Why Clinical Research Associate Programme?
Most clinical research graduates understand theory but lack real exposure to monitoring visits, site documentation, and CRO-level workflows.
This 6-week intensive program is designed to help life science graduates and professionals gain hands-on experience in real clinical trial monitoring processes used
in pharma and CROs.
Industry-Aligned Career Roles
Built for real clinical research careers Mapped to roles in CROs, pharma companies, hospitals, and global clinical operations teams.
Complete Monitoring Workflow
Learn the end-to-end monitoring cycle
From Site Selection & Initiation → Monitoring Visits → Source Data Verification (SDV) → Query Resolution → Close-Out reporting.
Mentorship + Practical Guidance
Industry demands compliance & clarity
Graduate with real monitoring reports, SIV documentation, and audit-ready templates.
Portfolio-Grade Capstone Project
One project that proves your skill
Complete a full mock Site Initiation Visit (SIV) and perform SDV with professional-grade documentation output.
Eligibility
Who This Program Is For
This program is designed for:
Life science graduates exploring clinical research, CRO, or pharma monitoring roles
MSc, PharmD, BPharm, and allied health graduates aiming for CRA or clinical operations careers
Professionals in hospitals, pharma, or CROs seeking structured clinical trial monitoring skills
Anyone who wants clarity before committing to a long-term postgraduate program in clinical research
Life science graduates exploring clinical research, CRO, or pharma monitoring roles
MSc, PharmD, BPharm, and allied health graduates aiming for CRA or clinical operations careers
Professionals in hospitals, pharma, or CROs seeking structured clinical trial monitoring skills
Anyone who wants clarity before committing to a long-term postgraduate program in clinical research
Life science graduates exploring clinical research, CRO, or pharma monitoring roles
MSc, PharmD, BPharm, and allied health graduates aiming for CRA or clinical operations careers
Professionals in hospitals, pharma, or CROs seeking structured clinical trial monitoring skills
Anyone who wants clarity before committing to a long-term postgraduate program in clinical research
Life science graduates exploring clinical research, CRO, or pharma monitoring roles
MSc, PharmD, BPharm, and allied health graduates aiming for CRA or clinical operations careers
Professionals in hospitals, pharma, or CROs seeking structured clinical trial monitoring skills
Anyone who wants clarity before committing to a long-term postgraduate program in clinical research
Outcomes
Career Outcomes and Roles
This program aligns you toward roles such as:
Clinical Research Associate
Clinical Trial Assistant
In-House / Remote CRA
Site Management Associate
Clinical Research Associate
Clinical Trial Assistant
In-House / Remote CRA
Site Management Associate
Clinical Research Associate
Clinical Trial Assistant
In-House / Remote CRA
Site Management Associate
Clinical Research Associate
Clinical Trial Assistant
In-House / Remote CRA
Site Management Associate
Syllabus
What you'll learn
You will learn how real bioinformatics analysts work inside R&D and pharma teams also trained to :
01
Week 01
Foundations & Clinical Trial Basics
Live: Introduction to Clinical Research & ICH-GCP Roles in Clinical Trials (Sponsor, CRO, Site) Clinical Trial Phases & Study Documents Protocol overview and Investigator responsibilities Async: Understanding essential documents (ICF, Protocol, IB) Overview of monitoring visits (PSV, SIV, MOV, COV) Capstone Prep: Select a mock study protocol and understand site requirements
01
Week 01
Foundations & Clinical Trial Basics
Live: Introduction to Clinical Research & ICH-GCP Roles in Clinical Trials (Sponsor, CRO, Site) Clinical Trial Phases & Study Documents Protocol overview and Investigator responsibilities Async: Understanding essential documents (ICF, Protocol, IB) Overview of monitoring visits (PSV, SIV, MOV, COV) Capstone Prep: Select a mock study protocol and understand site requirements
02
WEEK 02
Site Initiation & Documentation Control
Live: Site Selection & Feasibility basics Site Initiation Visit (SIV) process Trial Master File (TMF) & Investigator Site File (ISF) Regulatory documentation checklist Async: Review sample SIV report Study essential documents filing structure Capstone: Draft a mock SIV report and prepare site documentation checklist
02
WEEK 02
Site Initiation & Documentation Control
Live: Site Selection & Feasibility basics Site Initiation Visit (SIV) process Trial Master File (TMF) & Investigator Site File (ISF) Regulatory documentation checklist Async: Review sample SIV report Study essential documents filing structure Capstone: Draft a mock SIV report and prepare site documentation checklist
03
WEEK 03
Monitoring Visits & Source Data Verification
Live: Monitoring Visit workflow (MOV) Source Data Verification (SDV) process Case Report Forms (CRF) & EDC systems overview Query generation and resolution Async: Practice SDV on dummy patient case Write monitoring observation notes Capstone: Complete SDV exercise and generate monitoring findings report
03
WEEK 03
Monitoring Visits & Source Data Verification
Live: Monitoring Visit workflow (MOV) Source Data Verification (SDV) process Case Report Forms (CRF) & EDC systems overview Query generation and resolution Async: Practice SDV on dummy patient case Write monitoring observation notes Capstone: Complete SDV exercise and generate monitoring findings report
04
WEEK 04
Adverse Events & Safety Reporting
Live: Adverse Event (AE) vs Serious Adverse Event (SAE) Safety reporting timelines Investigator responsibilities in safety reporting Overview of Pharmacovigilance coordination Async: Review sample SAE form and narrative format Understand reporting flow: Site → Sponsor → Regulatory Capstone: Draft a mock SAE narrative and prepare safety reporting documentation
04
WEEK 04
Adverse Events & Safety Reporting
Live: Adverse Event (AE) vs Serious Adverse Event (SAE) Safety reporting timelines Investigator responsibilities in safety reporting Overview of Pharmacovigilance coordination Async: Review sample SAE form and narrative format Understand reporting flow: Site → Sponsor → Regulatory Capstone: Draft a mock SAE narrative and prepare safety reporting documentation
05
WEEK 05
Close-Out Visits & Audit Readiness
Live: Close-Out Visit (COV) process Drug accountability and reconciliation Query resolution follow-up Inspection & audit preparedness basics Async: Review monitoring report templates Understand CAPA (Corrective & Preventive Action) basics Capstone: Prepare a Close-Out Visit summary and audit readiness checklist
05
WEEK 05
Close-Out Visits & Audit Readiness
Live: Close-Out Visit (COV) process Drug accountability and reconciliation Query resolution follow-up Inspection & audit preparedness basics Async: Review monitoring report templates Understand CAPA (Corrective & Preventive Action) basics Capstone: Prepare a Close-Out Visit summary and audit readiness checklist
06
WEEK 06
Capstone Finalization & Career Pathways
Live: How to present monitoring experience in interviews CRA resume structuring workshop Understanding CRO hiring process Common CRA interview scenarios Presentation: Present your full monitoring workflow: SIV → SDV → AE handling → COV documentation Capstone Output: Complete monitoring portfolio including: SIV report SDV documentation Monitoring findings report SAE narrative Close-Out checklist
06
WEEK 06
Capstone Finalization & Career Pathways
Live: How to present monitoring experience in interviews CRA resume structuring workshop Understanding CRO hiring process Common CRA interview scenarios Presentation: Present your full monitoring workflow: SIV → SDV → AE handling → COV documentation Capstone Output: Complete monitoring portfolio including: SIV report SDV documentation Monitoring findings report SAE narrative Close-Out checklist
WEEK 01
Foundations & Clinical Trial Basics
Live: Introduction to Clinical Research & ICH-GCP Roles in Clinical Trials (Sponsor, CRO, Site) Clinical Trial Phases & Study Documents Protocol overview and Investigator responsibilities Async: Understanding essential documents (ICF, Protocol, IB) Overview of monitoring visits (PSV, SIV, MOV, COV) Capstone Prep: Select a mock study protocol and understand site requirements
WEEK 01
Foundations & Clinical Trial Basics
Live: Introduction to Clinical Research & ICH-GCP Roles in Clinical Trials (Sponsor, CRO, Site) Clinical Trial Phases & Study Documents Protocol overview and Investigator responsibilities Async: Understanding essential documents (ICF, Protocol, IB) Overview of monitoring visits (PSV, SIV, MOV, COV) Capstone Prep: Select a mock study protocol and understand site requirements
WEEK 02
Site Initiation & Documentation Control
Live: Site Selection & Feasibility basics Site Initiation Visit (SIV) process Trial Master File (TMF) & Investigator Site File (ISF) Regulatory documentation checklist Async: Review sample SIV report Study essential documents filing structure Capstone: Draft a mock SIV report and prepare site documentation checklist
WEEK 03
Monitoring Visits & Source Data Verification
Live: Monitoring Visit workflow (MOV) Source Data Verification (SDV) process Case Report Forms (CRF) & EDC systems overview Query generation and resolution Async: Practice SDV on dummy patient case Write monitoring observation notes Capstone: Complete SDV exercise and generate monitoring findings report
WEEK 03
Monitoring Visits & Source Data Verification
Live: Monitoring Visit workflow (MOV) Source Data Verification (SDV) process Case Report Forms (CRF) & EDC systems overview Query generation and resolution Async: Practice SDV on dummy patient case Write monitoring observation notes Capstone: Complete SDV exercise and generate monitoring findings report
WEEK 04
Adverse Events & Safety Reporting
Live: Adverse Event (AE) vs Serious Adverse Event (SAE) Safety reporting timelines Investigator responsibilities in safety reporting Overview of Pharmacovigilance coordination Async: Review sample SAE form and narrative format Understand reporting flow: Site → Sponsor → Regulatory Capstone: Draft a mock SAE narrative and prepare safety reporting documentation
WEEK 04
Adverse Events & Safety Reporting
Live: Adverse Event (AE) vs Serious Adverse Event (SAE) Safety reporting timelines Investigator responsibilities in safety reporting Overview of Pharmacovigilance coordination Async: Review sample SAE form and narrative format Understand reporting flow: Site → Sponsor → Regulatory Capstone: Draft a mock SAE narrative and prepare safety reporting documentation
WEEK 05
Close-Out Visits & Audit Readiness
Live: Close-Out Visit (COV) process Drug accountability and reconciliation Query resolution follow-up Inspection & audit preparedness basics Async: Review monitoring report templates Understand CAPA (Corrective & Preventive Action) basics Capstone: Prepare a Close-Out Visit summary and audit readiness checklist
WEEK 05
Close-Out Visits & Audit Readiness
Live: Close-Out Visit (COV) process Drug accountability and reconciliation Query resolution follow-up Inspection & audit preparedness basics Async: Review monitoring report templates Understand CAPA (Corrective & Preventive Action) basics Capstone: Prepare a Close-Out Visit summary and audit readiness checklist
WEEK 06
Capstone Finalization & Career Preparation
Live: How to present monitoring experience in interviews CRA resume structuring workshop Understanding CRO hiring process Common CRA interview scenarios Presentation: Present your full monitoring workflow: SIV → SDV → AE handling → COV documentation Capstone Output: Complete monitoring portfolio including: SIV report SDV documentation Monitoring findings report SAE narrative Close-Out checklist
WEEK 06
Capstone Finalization & Career Preparation
Live: How to present monitoring experience in interviews CRA resume structuring workshop Understanding CRO hiring process Common CRA interview scenarios Presentation: Present your full monitoring workflow: SIV → SDV → AE handling → COV documentation Capstone Output: Complete monitoring portfolio including: SIV report SDV documentation Monitoring findings report SAE narrative Close-Out checklist
Syllabus
What you'll learn
You will learn how real bioinformatics analysts work inside R&D and pharma teams also trained to :
Program Fee
Enroll Once. Become Job-Ready in 6 Weeks.
Enroll Once. Become Job-Ready in
6 Weeks.
Exclusive Cohort
Early Bird
Designed for learners building industry-ready clinical monitoring skills.
₹8,000
Inclusive of GST
Total duration: 6 weeks
Total duration: 6 weeks
Total learning hours: 39 hours
Total learning hours: 39 hours
Live sessions: 7
Live sessions: 7
Asynchronous learning: 20
Asynchronous learning: 20
Capstone work: 1
Capstone work: 1
Final presentation: 2
Final presentation: 2
What Makes This Program Different
A structured roadmap to start a career as a Clinical Research Associate
A structured roadmap to start a career as a Clinical Research Associate
Hands-on exposure to monitoring visits (SIV, MOV, COV) and SDV
Hands-on exposure to monitoring visits (SIV, MOV, COV) and SDV
Practical understanding of ICH-GCP guidelines and trial documentation
Learn what's used latest tools to build computational models & execute functions.
Real-world simulation of site initiation and monitoring workflows
Why are Bioinformaticians in demand,
salary-ranges & career paths
A complete capstone portfolio including SIV report and SDV documentation
A complete capstone portfolio including SIV report and SDV documentation
Confidence to clear CRA interviews and
work with CRO/site teams
Bioinformatician's Most Powerful Weapon - An insider look into the Industry
Meet our learners trained on real-world AI & healthcare workflows, equipped with industry-grade skills and practical experience to deliver impact from day one.
Industry-Ready Talent
Our Alumni
Meet our learners trained on real-world AI & healthcare workflows, equipped with industry-grade skills and practical experience to deliver impact from day one.
Industry-Ready Talent
Our Alumni
Frequently asked questions
1. What is the duration of the CRA Program?
The program runs for 6 weeks in a structured, part-time format designed to fit alongside college or work commitments.
2. What is the structure of the program?
3. How is this program different from a traditional degree or certification?
4. Who is this program meant for?
5. What kind of career outcomes can participants expect?
6. What topics and tools are covered in the program?
Frequently asked questions
1. What is the duration of the CRA Program?
The program runs for 6 weeks in a structured, part-time format designed to fit alongside college or work commitments.
3. How is this program different from a traditional degree or certification?
2. What is the structure of the program?
4. Who is this program meant for?
5. What kind of career outcomes can participants expect?
6. What topics and tools are covered in the program?
Frequently asked questions
1. What is the duration of the CRA Program?
The program runs for 6 weeks in a structured, part-time format designed to fit alongside college or work commitments.
3. How is this program different from a traditional degree or certification?
2. What is the structure of the program?
4. Who is this program meant for?
5. What kind of career outcomes can participants expect?
6. What topics and tools are covered in the program?
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