Quanticate Clinical Data Coordinator II Jobs
- Clinical Data Coordinator II vacancies at Quanticate, Bengaluru.
- Company Overview
- Job Role & Responsibilities
- Core Clinical Data Management Responsibilities
- Compliance, Quality & Collaboration
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Frequently Asked Questions
- Is this role suitable for freshers?
- Is this an on-site position?
- Which CDM systems are required?
- Are there growth opportunities?
- Does Quanticate charge any fees during hiring?
Clinical Data Coordinator II vacancies at Quanticate, Bengaluru.
Clinical Data Management is a critical function in clinical research, ensuring that high-quality, reliable data supports regulatory submissions and patient safety decisions. Quanticate is hiring a Clinical Data Coordinator II for its Bengaluru office. This role is ideal for experienced clinical data professionals who want hands-on involvement across the full lifecycle of clinical trials while working with a globally respected, data-focused CRO.
Company Overview
Quanticate is a world-leading data-focused Contract Research Organization specializing in biostatistics, statistical programming, and clinical data management. The company partners with global pharmaceutical companies, biotechnology firms, and emerging biotechs to support complex clinical trials requiring advanced data and statistical expertise.
Quanticate operates as an extension of its clients’ teams, providing high-quality, compliant, and efficient data solutions. Known for its strong scientific culture, regulatory rigor, and commitment to professional development, Quanticate supports clinical programs ranging from early development to late-phase global trials.
Job Role & Responsibilities
The Clinical Data Coordinator II role is a full-time, on-site position responsible for supporting end-to-end Clinical Data Management activities across multiple clinical studies.
Core Clinical Data Management Responsibilities
• Support full lifecycle Clinical Data Management activities from study start-up to close-out • Assist with database testing, user acceptance testing, and validation prior to study activation • Prepare, review, and maintain study-specific Data Management documentation • Perform critical review of Case Report Forms to identify inconsistencies, errors, and missing data • Raise, track, and resolve data queries and Data Clarification Forms • Manage self-evident queries and allowable data changes within clinical databases • Perform quality control checks on data entry and database outputs • Support study close-out activities, including preparation of archival documentation
Compliance, Quality & Collaboration
• Ensure compliance with SOPs, ICH-GCP guidelines, regulatory requirements, and client standards • Perform medical coding activities when assigned • Collaborate with offshore data processing and statistical programming teams • Support progress tracking using reports, metrics, and study dashboards • Contribute to process improvement initiatives and clinical data management best practices • Provide regular project updates to study teams and stakeholders • Support ad-hoc tasks to meet project and team objectives
Eligibility / Qualifications
This role is suitable for professionals with prior experience in clinical data management.
Required qualifications:
• Bachelor’s or Master’s degree in Life Sciences or a related discipline • Prior experience in Clinical Data Management or a similar role • Hands-on experience with at least one CDM system such as Medidata Rave, Oracle Clinical, or Inform • Strong understanding of Clinical Data Management processes • Knowledge of ICH-GCP guidelines and regulatory requirements related to data handling • Familiarity with CRO and sponsor-driven clinical trial standards • Proficiency in Microsoft Word and Excel
Relevant educational background includes: BSc Life Sciences, MSc Life Sciences, Clinical Research, Biotechnology, Pharmacy, Biostatistics
Location & Salary
Job Location: Bengaluru, Karnataka
This is a full-time, on-site role based in Bengaluru. Salary details are not publicly disclosed; however, Quanticate offers competitive compensation packages aligned with Clinical Data Management roles in the CRO industry.
Benefits typically include:
• Competitive salary • Flexible working hours • Medical insurance for self and immediate family • Paid annual, sick, casual, and bank holidays • Gratuity and accidental coverage • Access to mentoring, coaching, e-learning, and job shadowing programs
Application Process
Interested candidates can apply directly through the official Quanticate job posting using the link below:
Apply Online: https://www.linkedin.com/jobs/view/4369475581/
Shortlisted candidates will be contacted by the recruitment team for further steps in the hiring process.
Frequently Asked Questions
Is this role suitable for freshers?
No. This role requires prior experience in Clinical Data Management.
Is this an on-site position?
Yes. This is an on-site, full-time role in Bengaluru.
Which CDM systems are required?
Experience with systems such as Medidata Rave, Oracle Clinical, or Inform is required.
Are there growth opportunities?
Yes. Professionals can progress into senior CDM, lead, or project oversight roles.
Does Quanticate charge any fees during hiring?
No. Quanticate does not request any payments as part of the recruitment process
| Category | Details |
|---|---|
| Company | Quanticate |
| Vacancies | Clinical Data Coordinator II |
| Required Education | Life Sciences, Pharmacy, Clinical Research |
| Experience | Experienced |
To apply for this job please visit www.linkedin.com.
