QUANTICATE Hiring Clinical Data Coordinator II in Bengaluru, India | Clinical Data Management Jobs 2026
Job Title: Clinical Data Coordinator II
Company: Quanticate
Location: Bengaluru
Job Type: Full-Time
Department: Clinical Data Management
Work Mode: On-Site
Experience Required: 2–5 Years of Clinical Data Management Experience Preferred
Industry: Clinical Research | CRO | Pharmaceutical Services
About Quanticate
Quanticate is a globally recognized data-focused Contract Research Organization (CRO) specializing in Clinical Data Management, Biostatistics, Statistical Programming, and Clinical Trial Support Services. The company partners with leading global pharmaceutical organizations and emerging biotech companies to support complex clinical development programs worldwide.
Quanticate is known for delivering high-quality, regulatory-compliant clinical research solutions while promoting employee growth, continuous learning, and long-term career development within the pharmaceutical and healthcare industry.
Clinical Data Coordinator II Job Opening in Bengaluru
Quanticate is actively hiring experienced Clinical Data Management professionals for the position of Clinical Data Coordinator II in Bengaluru, Karnataka. This opportunity is ideal for candidates passionate about clinical research, data quality, regulatory compliance, and end-to-end clinical trial data management activities.
Professionals with prior experience in Clinical Data Management (CDM), database validation, query management, CRF review, and clinical database systems are encouraged to apply.
Key Responsibilities
Clinical Data Management Activities
Support end-to-end Clinical Data Management activities across multiple clinical studies
Assist with clinical database testing, validation, and study activation activities
Prepare, review, and maintain study-specific Data Management documentation
Ensure high-quality clinical trial data throughout the study lifecycle
CRF Review & Data Validation
Review Case Report Forms (CRFs) for missing, inconsistent, or incorrect clinical data
Identify discrepancies and raise Data Clarification Forms (DCFs)
Track, manage, and resolve clinical data queries efficiently
Perform quality control checks on database outputs and data entry activities
Database & Coding Support
Manage self-evident queries and permissible data modifications within CDM systems
Support medical coding activities whenever required
Collaborate with offshore programming and data processing teams
Study Close-Out & Compliance
Support study lock and archival documentation activities
Ensure compliance with SOPs, ICH-GCP guidelines, sponsor requirements, and regulatory standards
Contribute to process improvement initiatives and operational excellence programs
Project Coordination
Assist with project progress tracking using reports, metrics, and study dashboards
Coordinate effectively with cross-functional global clinical teams
Perform additional project-related responsibilities as assigned
Required Qualifications
Educational Qualification
Bachelor’s or Master’s degree in:
Pharmacy
Life Sciences
Biotechnology
Clinical Research
Biomedical Sciences
Related Healthcare Discipline
Experience Required
Preferred experience: 2–5 years in Clinical Data Management or related clinical research roles
Experience working within CROs, pharmaceutical companies, or clinical research environments is highly preferred
Candidates with hands-on experience supporting multiple clinical studies will have an advantage
Required Skills & Technical Competencies
Clinical Data Management Skills
Strong understanding of Clinical Data Management processes and workflows
Knowledge of ICH-GCP guidelines and regulatory compliance standards
Familiarity with sponsor-driven and CRO-based clinical trial environments
CDM Systems Knowledge
Hands-on experience with at least one of the following Clinical Data Management systems:
Oracle Clinical
Medidata Rave
Inform
Other EDC/CDM platforms
Core Professional Skills
Strong analytical and problem-solving abilities
Excellent attention to detail
Effective written and verbal communication skills
Ability to manage deadlines in fast-paced clinical environments
Strong organizational and time-management skills
Team collaboration and stakeholder coordination abilities
Proficiency in Microsoft Excel and Microsoft Word
Why Join Quanticate?
Career Growth Opportunities
Exposure to complete Clinical Data Management lifecycle activities
Opportunity to work on global clinical trials and international projects
Structured learning and professional development environment
Learning & Development
Mentoring and coaching programs
E-learning and job shadowing opportunities
Professional society memberships and career advancement support
Global Clinical Exposure
Work alongside cross-functional global teams
Collaborate with top pharmaceutical and biotechnology companies
Gain practical experience in regulated clinical research operations
Employee Benefits
Competitive Salary Package
Flexible Working Hours
Annual Leave, Casual Leave, Sick Leave & Bank Holidays
Medical Insurance for Employee and Immediate Family
Gratuity Benefits
Accidental Insurance Coverage
Continuous Learning & Development Programs
Mentorship and Career Progression Opportunities
Important Recruitment Notice
Quanticate does not request payment, deposits, or paid training/course fees during any stage of the recruitment or hiring process. All official communication is conducted only through the official @quanticate.com email domain.
Candidates are advised to stay alert against fraudulent recruitment activities and apply only through verified company channels.
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