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Receive the syllabus, fee details, online batch timing, dual certification information and internship pathway.
A clear overview of BCRI’s online advanced certification for students comparing CRA training, CRC training and Clinical Data Management training.
| Course Name | Online Advanced Certification in CRA, CRC & Clinical Data Management |
| Learning Mode | Live online / online supported learning with LMS access and practical case discussions |
| Core Domains | Clinical Research, CRA Training, CRC Training, Clinical Data Management, EDC, SDV, TMF/eTMF, Query Management |
| Certification | BCRI certification + NSDC–LSSSDC / NCVET / NSQF-based certification pathway, subject to applicable assessment and eligibility |
| Internship Option | 3-month or 6-month internship opportunity; paid or unpaid depending on partner company/project availability |
| Career Areas | SMOs, CROs, hospitals, clinical trial sites, pharma companies and clinical data management teams |
Learn monitoring visit preparation, SDV, site follow-up, protocol compliance, audit readiness, TMF/eTMF and sponsor/CRO communication.
Learn patient visit coordination, informed consent support, source documentation, AE/SAE documentation and site-level trial operations.
Learn EDC workflow, eCRF design, data entry, query management, discrepancy handling, data cleaning, reconciliation, QC and database lock.
Watch this step-by-step Clinical Data Management demo to understand how clinical trial data is reviewed, entered, cleaned and prepared for analysis. This video helps students of the Advanced CRA, CRC and CDM Course understand practical CDM workflow, CRF/eCRF handling, query management and real job responsibilities in clinical research.
Confirms completion of BCRI’s online Advanced CRA, CRC and Clinical Data Management course covering clinical research operations, site coordination, monitoring and CDM workflows.
Eligible students may undergo NSDC–LSSSDC / NCVET / NSQF-based assessment where applicable, subject to qualification pack mapping, batch eligibility and assessment process.
Students taking a 3-month or 6-month internship may receive an industry exposure or internship certificate from the host organisation, based on completion and company policy.
Suitable for students who want shorter practical exposure after completing online CRA, CRC and Clinical Data Management training.
Suitable for students who want deeper industry exposure and stronger job readiness for CRA, CRC, trial assistant and CDM roles.
Internships may be paid or unpaid depending on company/project availability. High-performing candidates may get absorbed in the same company based on performance, vacancy and hiring policy.
Clinical research overview, phases, study designs, ethics, ICH-GCP, regulatory authorities, protocol, ICF, CRF and essential documents.
Patient coordination, screening, enrolment, visit scheduling, source documents, site file maintenance, AE/SAE documentation and investigator support.
Pre-study visit, site initiation visit, interim monitoring visit, close-out visit, SDV, SDR, RBM, deviation handling and monitoring follow-up.
DMP, study setup, eCRF specification, database design, DVS, UAT, EDC data entry, edit checks, system queries and manual queries.
Discrepancy management, DCM/DCI concepts, listing review, consistency checks, lab data review, SAE reconciliation, IxRS reconciliation and QC reports.
Resume preparation, mock interviews, job role guidance, internship counselling and placement support for SMOs, CROs, hospitals and CDM teams.
Clinical Research Coordinator, Study Coordinator, Site Coordinator, Trial Assistant, Patient Recruitment Coordinator, Site Documentation Executive.
CRA Trainee, Junior CRA, Clinical Trial Assistant, Clinical Operations Associate, Site Management Associate, TMF/eTMF Associate.
Hospital Research Coordinator, Clinical Trial Coordinator, Research Nurse, Trial Nurse, Ethics Committee Coordinator, Documentation Coordinator.
Clinical Data Coordinator, Clinical Data Associate, CDM Trainee, EDC Associate, Query Management Associate, Data Review Associate.
| Role | Fresher / Entry-Level Range | Growth Range | Best Entry Pathway |
|---|---|---|---|
| Clinical Research Coordinator / Study Coordinator | ₹2.4 LPA – ₹4.5 LPA | ₹4 LPA – ₹7.5 LPA | SMO, hospital or clinical trial site internship |
| CRA Trainee / Junior Clinical Research Associate | ₹3 LPA – ₹5 LPA | ₹5 LPA – ₹9 LPA | CRA training + monitoring knowledge + SDV practice |
| Clinical Data Associate / Clinical Data Coordinator | ₹3 LPA – ₹5 LPA | ₹5 LPA – ₹9 LPA | CDM training + EDC + query management practice |
| Senior CRA / Experienced CRA | Experience required | ₹9 LPA – ₹16 LPA+ | Monitoring experience + site management + audit readiness |
| Clinical Data Manager | Experience required | ₹8 LPA – ₹15 LPA+ | CDM experience + database lock + team/project coordination |
Overview of clinical research, clinical studies vs clinical trials, stakeholders, sponsors, CROs, SMOs, investigators, sites, ethics committees and career opportunities.
Phase 0, Phase I, Phase II, Phase III, Phase IV, post-marketing studies, SAD, MAD, dose-ranging studies, interventional, observational and trial design basics.
ICH-GCP principles, informed consent, participant protection, ethics committee/IRB review, DCGI/CDSCO, FDA, EMA, IND, NDA, ANDA, confidentiality, GDPR and HIPAA overview.
Protocol, Investigator’s Brochure, ICF, CRF/eCRF, source documents, delegation log, screening log, enrolment log, Trial Master File, Investigator Site File and archival.
Site coordination, patient visit scheduling, screening, enrolment, source documentation, AE/SAE documentation support, lab report coordination and site close-out support.
CRA responsibilities, site management, pre-study visit, site initiation visit, interim monitoring visit, close-out visit, monitoring reports, follow-up letters and action item tracking.
Source Data Verification, Source Data Review, RBM, remote monitoring, centralized monitoring, protocol deviation/violation, CAPA basics and audit readiness.
AE vs SAE, SAE reporting responsibilities, safety documentation, SAE reconciliation, safety committees and AE/SAE data collection in EDC.
Data Management Plan, study setup, eCRF specifications, database design, DVS, edit checks, UAT, final sign-off, EDC access, data entry and query management.
Listing review, discrepancy management, DCM/DCI concepts, lab data review, SAE reconciliation, IxRS reconciliation, vendor reconciliation, QC reports, database lock and archival.
CTMS, trial tracking, eTMF, EDC integration, IVRS/IWRS, remote monitoring tools, decentralized clinical trials and technology-driven clinical trial operations.
Resume preparation, LinkedIn profile guidance, mock interviews, job role mapping, internship guidance and interview preparation for CRA, CRC and CDM roles.
Protocol, ICF, Investigator’s Brochure, CRF/eCRF, source documents, delegation log, screening log, enrolment log, monitoring visit report and TMF/eTMF.
EDC, CTMS, eTMF, IVRS/IWRS, Remote Data Capture, query management tools and clinical trial tracking systems.
Site initiation, SDV, monitoring, AE/SAE documentation, EDC data entry, discrepancy management, reconciliation, QC and database lock.
Practice reading protocol sections, visit schedules, inclusion/exclusion criteria and informed consent documentation.
Understand source data verification, monitoring visit preparation, site follow-up, query tracking and deviation documentation.
Practice EDC data entry logic, system queries, manual queries, query response, discrepancy handling and query closure.
Learn AE/SAE collection, safety documentation, SAE reconciliation and safety data quality responsibilities.
Learn listing review, consistency checks, data validation, reconciliation, QC status reports and database lock support.
Prepare for CRA Trainee, CRC, Clinical Data Associate, EDC Associate and Clinical Trial Assistant interviews.
| Normal CRA/CRC Course | BCRI Advanced CRA, CRC & Clinical Data Management Course |
|---|---|
| Mostly focuses on site coordination and monitoring basics. | Covers site coordination, monitoring, clinical trial documentation and complete CDM workflow. |
| Limited exposure to EDC, eCRF, query management and database lock. | Includes EDC workflow, eCRF, data cleaning, discrepancy handling, reconciliation, QC and database lock. |
| Career focus may be limited to CRC or CRA trainee roles. | Students can target CRA, CRC, Clinical Trial Assistant, CDM, EDC, TMF/eTMF and clinical operations roles. |
| May not include internship pathway or dual certification clarity. | Includes 3/6-month internship option and BCRI + NSQF-based dual certification pathway, subject to eligibility and assessment. |
Get syllabus, fee, batch timing and eligibility guidance.
Ask about 3-month or 6-month internship options.
Yes. This page is for BCRI’s online Advanced Certification in CRA, CRC & Clinical Data Management. It combines Clinical Research Associate training, Clinical Research Coordinator training and Clinical Data Management training.
Yes. Freshers from pharmacy, life sciences, nursing, biotechnology, microbiology, allied health and healthcare backgrounds can join. The course starts from clinical research basics and gradually moves into CRA, CRC and CDM workflows.
A CRA monitors clinical trial sites and checks compliance. A CRC coordinates trial activities at the site. A CDM professional manages clinical trial data through EDC, query management, data cleaning, reconciliation, QC and database lock.
Eligible students may get access to 3-month or 6-month internship opportunities through available SMO, CRO, hospital, clinical research site or partner company openings.
The internship may be paid or unpaid depending on company policy, project availability, student selection, duration and performance.
There may be an opportunity for absorption, but it depends on performance, vacancy, interview outcome and company hiring policy. It should not be treated as a guaranteed placement.
NSQF/NCrF-aligned learning may support academic credit value where applicable. Credit transfer, ABC storage or score addition depends on assessment completion, awarding body rules and acceptance by the student’s university or academic institution.
Students can apply for CRA Trainee, Clinical Research Coordinator, Clinical Trial Assistant, Clinical Data Associate, Clinical Data Coordinator, EDC Associate, TMF Associate, Site Coordinator and Clinical Operations Executive roles.
Yes. The course includes EDC workflow, eCRF, SDV, TMF/eTMF, query management, discrepancy handling, data cleaning, reconciliation, QC and database lock concepts.
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