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Clinical Trial Coordinator Job Bioplus Life Sciences Hiring Now!

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Bioplus Life Sciences

B.Pharm / M.Pharm / M.Sc (Life Sciences/Biotechnology/Clinical Research) / B.Tech (Biotechnology)

Bangalore

3-4 years

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Bioplus Life Sciences is a leading pharmaceutical and clinical research organization dedicated to advancing drug development and clinical trials. With a strong focus on GCP compliance, regulatory standards (FDA/EMA), and patient-centric research, Bioplus offers a dynamic work environment for professionals in clinical operations, biotechnology, and life sciences.

๐Ÿ“ Location: Whitefield, Bangalore
๐Ÿ“Œ Industry: Clinical Research / Biotechnology
๐Ÿ”ฌ Key Focus Areas: Phase I-IV Trials, Regulatory Compliance, Patient Recruitment


Detailed Job Description

Job Title: Clinical Trial Coordinator

Department: Clinical Research / Clinical Operations
Job Type: Full-Time
Reports To: Clinical Operations Manager

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Key Responsibilities

โœ” Trial Coordination: Manage day-to-day clinical trial activities, ensuring protocol adherence and timeline compliance.
โœ” Patient Recruitment: Assist in subject screening, enrollment, and follow-up visits per study protocols.
โœ” Documentation: Maintain regulatory binders, source documents, and CRFs (Case Report Forms).
โœ” Data Management: Ensure accurate data entry in EDC systems (Electronic Data Capture) and resolve queries.
โœ” Stakeholder Communication: Liaise with sponsors, CROs (Contract Research Organizations), and study sites.
โœ” Regulatory Compliance: Assist in IRB submissions, amendments, and audit preparations.
โœ” Monitoring & Audits: Coordinate site visits, inspections, and data quality checks.
โœ” Study Metrics Tracking: Monitor recruitment rates, patient retention, and trial progress.


Eligibility Criteria

Education:

  • B.Pharm / M.Pharm / M.Sc (Life Sciences/Biotechnology/Clinical Research) / B.Tech (Biotechnology)
  • Certification in Clinical Research (ACRP/SOCRA preferred)

Experience:

  • 3-4 years in clinical research or trial coordination
  • Knowledge of GCP, ICH guidelines, FDA/EMA regulations
  • Familiarity with EDC systems, CTMS (Clinical Trial Management Systems)

Preferred Qualifications:

  • Experience inย Phase I-IV trials
  • Background inย hospitals, academia, or CROs
  • Strongย organizational, communication, and problem-solving skills

Benefits & Work Environment

โœ… Competitive salary & growth opportunities
โœ… Exposure to global clinical trials & regulatory standards
โœ… Collaborative work culture with industry experts
โœ… Flexible hours (as per study demands)
โœ… Travel opportunities to clinical sites/sponsor meetings


How to Apply

๐Ÿ“ฉ Email your resume to: talent@bioplus.in
๐Ÿ“ Job Location: Whitefield, Bangalore

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