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Advanced Certification in Clinical Research Associate, Clinical Research Coordinator & Clinical Data Management
Join BCRI’s offline classroom-based CRA CRC CDM course in Bangalore and build job-ready skills in clinical trial operations, site coordination, monitoring, EDC, SDV, TMF/eTMF, query management and clinical data workflows.
Get offline batch timing, syllabus, fee details and internship guidance for the Bangalore classroom batch.
A classroom-based clinical research course designed for students who want practical training, local mentor support and career guidance for CRA, CRC and Clinical Data Management roles in Bangalore.
| Course Feature | Offline Bangalore Course Details |
|---|---|
| Course Name | Advanced Certification in CRA, CRC & Clinical Data Management |
| Location | BCRI Training Centre, HSR Layout, Bangalore |
| Best For | Life science, pharmacy, nursing, medical, biotechnology, microbiology and allied healthcare graduates |
| Training Mode | Offline classroom training with practical examples, trainer interaction and guided career counselling |
| Core Skills | Clinical research, CRA responsibilities, CRC responsibilities, EDC, SDV, TMF/eTMF, eCRF, query management and Clinical Data Management |
| Internship Pathway | Eligible learners may apply for 3-month or 6-month internship opportunities with available SMO, CRO, hospital or clinical research site partners |
| Certification | BCRI certification with NSDC–LSSSDC / NCVET / NSQF-based assessment pathway, subject to eligibility and applicable assessment process |
Bangalore is a strong location for clinical research learning because students can explore opportunities across hospitals, SMOs, CROs, healthcare companies, clinical trial sites and clinical data teams.
Learn through offline trainer-led sessions with structured schedules, peer interaction and direct doubt clarification.
Convenient for learners from HSR Layout, BTM Layout, Koramangala, Electronic City, Sarjapur Road, Bellandur, Marathahalli, Whitefield and JP Nagar.
Understand both site-level clinical trial work and data management workflows, instead of learning only one narrow role.
This offline CRA CRC CDM course in Bangalore helps students understand how clinical trial teams work together from patient visit and source documentation to EDC data entry, query resolution and database lock.
Learn monitoring visit types, SDV, site follow-up, protocol compliance, TMF/eTMF, action items and audit readiness.
Learn patient visit coordination, informed consent support, source documents, AE/SAE documentation and site file maintenance.
Learn EDC workflow, eCRF, data entry, query management, discrepancy handling, reconciliation, QC and database lock.
Use this section for a classroom video, demo lecture, trainer introduction or student testimonial video. The goal is to show that BCRI’s offline CRA CRC and Clinical Data Management course gives students a guided learning environment at HSR Layout, Bangalore.
Replace the video link with your actual BCRI classroom, course introduction or student feedback video.
This offline Advanced Certification in CRA, CRC & Clinical Data Management is positioned as a dual certification pathway for eligible students, combining BCRI course completion certification with skill-based assessment opportunities.
Awarded after successful completion of BCRI’s CRA, CRC and Clinical Data Management training curriculum.
Eligible learners may undergo NSDC–LSSSDC assessment based on applicable job-role mapping and batch eligibility.
NSQF-based certification helps demonstrate structured job-role competency, subject to assessment and awarding body rules.
The curriculum is built to help students understand the full clinical trial workflow from site operations to EDC data management and database lock.
Mode: Offline classroom training
Location: HSR Layout, Bangalore
Focus: CRA + CRC + CDM
Practical Areas: EDC, SDV, TMF/eTMF, eCRF, query management and database lock
Internship: 3 or 6 months pathway, subject to availability and selection
Overview of clinical research, clinical study vs clinical trial, clinical trial stakeholders, sponsors, CROs, SMOs, investigators, ethics committees and regulatory authorities.
Phase 0 to Phase IV trials, post-marketing studies, exploratory studies, safety and efficacy trials, SAD, MAD, microdosing, randomized, blinded, open-label and crossover designs.
ICH-GCP principles, informed consent, ethics committee process, participant protection, DCGI, CDSCO, FDA, EMA, IND, NDA, ANDA, privacy and confidentiality basics.
Protocol, Investigator’s Brochure, ICF, CRF, eCRF, source documents, delegation log, screening log, enrollment log, Trial Master File, Investigator Site File and archival.
Patient screening, recruitment, retention, informed consent support, visit scheduling, lab coordination, source documentation, site file maintenance, AE/SAE documentation and site close-out support.
CRA responsibilities, site communication, visit preparation, pre-study visit, site initiation visit, interim monitoring visit, close-out visit, follow-up letters and action item tracking.
Clinical monitoring, Source Data Verification, Source Data Review, Risk-Based Monitoring, remote monitoring, centralized monitoring, protocol deviations, CAPA and audit readiness.
AE vs SAE, seriousness criteria, safety documentation, SAE reporting responsibilities, SAE reconciliation, safety committees and AE/SAE data collection in EDC.
Data Management Plan, study setup, data collection, tracking, database design, data validation, discrepancy management, data cleaning, query management, QC and database lock.
eCRF specifications, CRF design considerations, EDC workflow, data entry, system queries, manual queries, query response, query closure, edit checks and User Acceptance Testing.
SAE reconciliation, lab data reconciliation, IxRS reconciliation, vendor data reconciliation, final subject visit completion, database review, database lock checklist and archival.
CTMS, eTMF, EDC integration, IVRS/IWRS, Risk-Based Monitoring tools, remote monitoring and decentralized clinical trial overview.
Eligible students may get internship assistance through available SMO, CRO, hospital, clinical research site or partner organization opportunities in Bangalore and nearby locations.
Suitable for students who want short-term practical exposure after classroom training, subject to selection and available openings.
Suitable for deeper clinical research exposure, stronger workplace discipline and better job readiness, subject to company/project availability.
Internship may be paid or unpaid depending on host company policy, project type, internship duration and candidate performance.
Students may receive internship or industry exposure certification from the host organization after successful completion.
High-performing students may get an opportunity to continue in the same company depending on vacancy, performance and hiring policy.
Internship may include documentation, site coordination, EDC exposure, query support, source document review or trial operations support.
This course is designed to open multiple entry-level career routes across SMOs, CROs, hospitals, clinical trial sites and clinical data management teams.
Roles: Clinical Research Coordinator, Site Coordinator, Study Coordinator, Trial Coordinator, Research Assistant, Patient Recruitment Coordinator, Site Documentation Executive.
Work: Patient visits, informed consent support, source documents, AE/SAE documentation, site file maintenance and sponsor/CRO coordination.
Roles: CRA Trainee, Junior CRA, Clinical Trial Assistant, Clinical Operations Associate, Site Management Associate, TMF/eTMF Associate, Clinical Data Associate and EDC Associate.
Work: Monitoring support, SDV, site follow-up, TMF/eTMF filing, trial trackers, EDC query tracking and data review support.
Roles: Hospital Research Coordinator, Clinical Trial Coordinator, Trial Nurse, Ethics Committee Coordinator, Clinical Research Assistant and Documentation Coordinator.
Work: Investigator coordination, patient scheduling, lab coordination, source documentation, ICF support and site-level trial documentation.
Roles: Clinical Data Coordinator, Clinical Data Associate, Clinical Data Management Trainee, EDC Associate, Query Management Associate and Data Review Associate.
Work: EDC data review, query management, discrepancy handling, reconciliation, QC support and database lock activities.
Salary depends on qualification, communication skills, internship exposure, company type, city, role, interview performance and experience. These figures are indicative and not a guarantee.
| Role | Indicative Salary / Career Range |
|---|---|
| Clinical Research Coordinator / Study Coordinator | Entry-level roles often start around ₹2.4 LPA – ₹4.5 LPA, with higher growth based on city, hospital/site, experience and performance. |
| CRA Trainee / Clinical Research Associate | Glassdoor reports Clinical Research Associate salary in Bangalore around ₹4.75 LPA on average, with a typical range around ₹3.86 LPA – ₹7.75 LPA. |
| Clinical Data Associate / Coordinator | Clinical data roles commonly start around ₹3 LPA – ₹5 LPA and can grow with EDC, query management, reconciliation and database lock experience. |
| Senior CRA / Clinical Operations Growth | Experienced professionals may grow into Senior CRA, Site Manager, Clinical Operations Lead, Project Coordinator or Trial Manager roles. |
This classroom-based program is suitable for students and graduates who want to enter clinical research, clinical trial operations, site coordination or clinical data management roles.
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This course is designed to give wider employability because it combines site operations, clinical monitoring and clinical data management skills.
| Normal CRA/CRC Course | BCRI Offline Advanced CRA CRC CDM Course |
|---|---|
| Focuses mainly on site and monitoring concepts | Covers CRA, CRC and Clinical Data Management together |
| Limited EDC and data management exposure | Includes EDC, eCRF, query management, discrepancy handling and database lock |
| May not connect site work with data workflows | Explains how patient visit data moves from site to EDC and data cleaning teams |
| Often more theoretical | Uses classroom discussion, role-based learning, practical examples and internship guidance |
| Limited career direction | Prepares students for SMO, CRO, hospital, clinical operations and CDM roles |
Replace these placeholders with genuine student reviews from BCRI learners after collecting permission.
★★★★★
The offline CRA CRC and Clinical Data Management course at BCRI Bangalore helped me understand clinical trial operations, site coordination, EDC and query management in a structured way.
B.Pharm Graduate
★★★★★
I joined BCRI for Clinical Research Associate and Clinical Research Coordinator training in Bangalore. The classroom learning and practical examples made the concepts easier to understand.
Life Science Graduate
★★★★★
The Clinical Data Management part was useful for understanding EDC, eCRF, discrepancy management, reconciliation and database lock. Good course for freshers in Bangalore.
M.Sc Biotechnology Graduate
Common questions from students searching for clinical research, CRA, CRC and Clinical Data Management training in Bangalore.
The offline course is conducted at BCRI’s training centre in HSR Layout, Bangalore. It is convenient for students from HSR Layout, BTM Layout, Koramangala, Electronic City, Sarjapur Road, Bellandur, Marathahalli, Whitefield, JP Nagar and nearby areas.
Yes. This page is for BCRI’s offline classroom-based Advanced Certification in CRA, CRC & Clinical Data Management in Bangalore.
You will learn clinical monitoring, pre-study visit, site initiation visit, interim monitoring visit, close-out visit, Source Data Verification, TMF/eTMF, site follow-up, protocol deviations and audit readiness.
You will learn patient visit coordination, informed consent support, source documentation, AE/SAE documentation, site file maintenance, lab coordination and communication with investigators, sponsors and CROs.
Yes. The course includes EDC workflow, eCRF, data entry, query management, discrepancy handling, validation, reconciliation, QC and database lock concepts.
Eligible students may get access to 3-month or 6-month internship opportunities through available SMO, CRO, hospital, clinical research site or partner organization openings. Internship availability depends on selection and company/project requirements.
The internship may be paid or unpaid depending on the host organization, project type, duration, student selection and available openings.
There may be an opportunity for absorption in the same company, but it depends on student performance, vacancy, interview outcome and company hiring policy.
Students receive BCRI certification after successful completion and may also be eligible for NSDC–LSSSDC / NCVET / NSQF-based certification assessment, subject to applicable job-role mapping, assessment process and batch eligibility.
Life science, pharmacy, nursing, medical, biotechnology, microbiology, biochemistry and allied healthcare graduates can join. Freshers can also join because the course starts from clinical research basics.
Students can apply for roles such as Clinical Research Coordinator, CRA Trainee, Clinical Trial Assistant, Clinical Data Associate, Clinical Data Coordinator, EDC Associate, TMF Associate, Site Coordinator and Clinical Operations Executive.
Address:
#19/19, 2nd Floor, 24th Main Rd, HSR Layout, Sector 1, Bangalore – 560102.
Convenient for learners from HSR Layout, BTM Layout, Koramangala, Electronic City, Sarjapur Road, Bellandur, Marathahalli, Whitefield, JP Nagar and nearby Bangalore areas.
Join BCRI’s offline Advanced Certification in CRA, CRC & Clinical Data Management and prepare for clinical research, site coordination, monitoring and clinical data management roles through classroom training, dual certification pathway, internship guidance and placement support.
Speak with our advisor and understand the right career path: CRA, CRC, Clinical Trial Assistant, EDC Associate or CDM roles.
Get complete course details, upcoming offline batch timing and eligibility guidance.
Recognized Training Partner under Life Sciences Sector Skill Development Council
Live mentor support • Internship & placement assistance*
Our Team would love to Guide you to select the right course here .
