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Clinical Research Associate / Senior Cra

Remidio
Remidio
3-4 years
Not Disclosed
Bangalore, Bengaluru, India
10 May 7, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Clinical Research Associate / Senior CRA
Experience: 3–4 Years
Location: Bangalore
Employment Type: Full-Time


Who This Role Is For

This role is for an experienced, hands-on Clinical Research Associate who prioritizes disciplined execution, high-quality data, and audit-ready clinical trials.

You will:

  • Own site-level execution end-to-end

  • Ensure clinical trials are conducted exactly as per protocol

  • Minimize and resolve deviations proactively

  • Ensure data integrity for audits, analysis, and publication readiness


Key Responsibilities

1. Site Execution & Monitoring (Primary Ownership)

  • Own assigned clinical trial sites from initiation to close-out

  • Conduct:

    • Site Initiation Visits (SIVs)

    • Routine Monitoring Visits

    • Close-Out Visits (COVs)

  • Manage:

    • Patient recruitment and eligibility verification

    • Informed consent process

    • Patient follow-ups and compliance

  • Ensure adherence to:

    • Study protocols

    • Good Clinical Practice (GCP)

    • ICH guidelines

    • ISO 14155 standards

  • Identify risks, deviations, and non-compliance early and resolve proactively

  • Train and support:

    • Site staff

    • Junior coordinators

    • On protocol procedures, EDC systems, and GCP requirements

  • Collaborate with:

    • Sponsors

    • CROs (if applicable)

    • Investigators

    • Data management teams for study oversight and data reconciliation


2. Data Quality & Source Verification (Primary Ownership)

  • Perform rigorous Source Data Verification (SDV) and Source Data Review (SDR)

  • Ensure:

    • Data accuracy

    • Completeness

    • Timeliness

  • Manage:

    • Site-level queries

    • Follow-ups and closures

  • Ensure:

    • Source-to-EDC traceability

    • Proper contemporaneous documentation

  • Support database lock readiness through site-level data cleanup


3. Issue Management & CAPAs

  • Document:

    • Protocol deviations

    • Non-compliances

    • Adverse Events (AEs) and Serious Adverse Events (SAEs)

  • Support:

    • CAPA implementation at site level

    • Verification of CAPA effectiveness

  • Escalate issues only when necessary; resolve at site level whenever possible


4. Audit & Inspection Readiness

  • Ensure assigned sites are always inspection-ready

  • Support:

    • Internal audits

    • Sponsor audits

    • Regulatory inspections

  • Maintain complete and accurate Trial Master File (TMF) documentation


5. Collaboration & Communication

  • Assist with:

    • Regulatory submissions

    • IEC/IRB communications

    • SAE reporting

    • TMF maintenance

  • Work closely with:

    • Clinical Operations team

    • Data Quality Managers

  • Coordinate with investigators and site staff to improve:

    • Compliance

    • Data quality

  • Deliver:

    • Clear monitoring reports

    • Timely follow-ups on action items


Qualifications

Mandatory Requirements

  • 3–4 years of experience as a Clinical Research Associate

  • Strong hands-on experience in:

    • Site monitoring

    • SDV (Source Data Verification)

  • Strong understanding of:

    • GCP

    • ICH guidelines

    • ISO 14155

  • Experience with:

    • Electronic Data Capture (EDC) systems

    • Query management

  • Ability to independently manage multiple sites


Good to Have

  • Experience in medical device clinical trials

  • Exposure to audits or regulatory inspections

  • Experience supporting database lock activities

  • Knowledge of:

    • Python and SPSS for data validation, statistical reporting, and workflow automation

  • Support for:

    • Scientific abstracts

    • Statistical analysis reports

    • Investigator presentations

  • Experience in:

    • Protocol development

    • Manuscript drafting

    • Journal submissions