Quantitate Hiring Clinical Data Coordinator I in Bengaluru
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(Quanticate Hiring Clinical Data Coordinator) |
Introduction
The clinical research industry continues to create exciting career opportunities for professionals interested in Clinical Data Management, Clinical Operations, and Global Clinical Trials. As pharmaceutical and biotechnology companies expand their research activities worldwide, the demand for skilled Clinical Data Management professionals is growing rapidly.
Quanticate, a globally recognized Contract Research Organization (CRO), has announced recruitment for the Clinical Data Coordinator I position at its Bengaluru office. This opportunity is ideal for candidates who want to build a long-term career in Clinical Data Management while gaining exposure to international clinical studies, regulatory requirements, and advanced Electronic Data Capture (EDC) systems.
Professionals with experience in Oracle Clinical, Medidata Rave, and Inform, as well as ICH-GCP guidelines, are encouraged to apply.
About Quanticate
Quanticate is a leading data-focused Contract Research Organization (CRO) specializing in Clinical Data Management, Biostatistics, Statistical Programming, and Clinical Research Services. The company supports pharmaceutical, biotechnology, and healthcare organizations across multiple therapeutic areas worldwide.
Founded in 1994, Quanticate has established itself as a trusted partner for clinical development programs and data-driven clinical research solutions. The company is headquartered in Hitchin, Hertfordshire, United Kingdom, and operates globally through its international teams.
With hundreds of professionals working across various locations, Quanticate delivers high-quality clinical trial support services to global pharmaceutical and biotechnology sponsors.
The organization is known for its expertise in clinical data management, statistical programming, data science, and regulatory-compliant clinical research services.
Job Overview Summary
Quanticate is currently seeking a Clinical Data Coordinator I for its Bengaluru office. The selected candidate will support clinical data management activities across multiple studies and contribute to maintaining data quality, database accuracy, regulatory compliance, and study documentation.
This role offers excellent exposure to clinical trial database management, data validation, query management, CRF review, medical coding, and quality assurance activities.
Candidates interested in Clinical Data Management careers, Clinical Research jobs, Pharmacovigilance careers, Regulatory Affairs, and Clinical Operations roles can benefit significantly from this opportunity.
Vacancy Details
Company Name
Quanticate
Position
Clinical Data Coordinator I
Job Type
Full-Time
Workplace Type
On-Site
Industry
Clinical Research
Contract Research Organization (CRO)
Clinical Data Management
Job Location
Bengaluru, Karnataka, India
Job Role Explanation
The Clinical Data Coordinator I serves as an important member of the Clinical Data Management team and helps ensure that clinical trial data remains accurate, complete, and compliant with international regulatory standards.
The role involves reviewing clinical trial information, validating data entries, resolving discrepancies, managing data clarification processes, supporting database testing, and ensuring the quality of collected clinical research data.
This position provides valuable exposure to global clinical trial processes and offers a strong foundation for future growth within Clinical Data Management and Clinical Research domains.
Key Responsibilities
The selected candidate will be responsible for:
Clinical Data Management Activities
- Supporting clinical study database testing and validation.
- Assisting in study startup activities.
- Preparing study-specific documentation.
- Managing database quality checks.
- Supporting project closeout activities.
Data Review and Validation
- Reviewing clinical trial data for completeness.
- Validating collected study data.
- Identifying inconsistencies and discrepancies.
- Ensuring compliance with study protocols.
Query Management
- Raising data queries.
- Following up on outstanding queries.
- Resolving data discrepancies.
- Managing Data Clarification Forms (DCFs).
CRF Review Activities
- Reviewing Case Report Forms (CRFs).
- Verifying data consistency.
- Supporting clinical database quality control.
Medical Coding Activities
- Supporting medical coding assignments.
- Assisting with coding review processes.
- Maintaining coding accuracy and consistency.
Collaboration Activities
- Working with Project Managers.
- Coordinating with Sponsors.
- Supporting Investigators and Study Teams.
- Collaborating with global clinical research professionals.
Eligibility Criteria
Candidates applying for this role should possess:
Educational Qualification
- Bachelor's Degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related discipline preferred.
Experience Requirements
- Previous experience in Clinical Data Management or related functions.
- Experience supporting clinical studies preferred.
- Experience with multiple clinical projects will be an added advantage.
Knowledge Requirements
- Clinical Data Management Processes.
- Clinical Trial Operations.
- ICH-GCP Guidelines.
- Regulatory Compliance Requirements.
- CRO Environment Understanding.
Skills Required
Successful candidates should possess the following skills:
Technical Skills
- Clinical Data Management
- Clinical Trial Data Review
- Data Validation
- Query Management
- Database Testing
- Medical Coding
- Data Quality Review
- CRF Review
- Regulatory Compliance
- Clinical Documentation
Software Skills
Experience with:
- Oracle Clinical
- Medidata Rave
- Inform
- Microsoft Excel
- Microsoft Word
Soft Skills
- Attention to Detail
- Analytical Thinking
- Problem Solving
- Communication Skills
- Team Collaboration
- Time Management
- Organizational Skills
Salary Estimate
Quanticate has not officially disclosed the salary package for this role.
Based on current Clinical Data Management market standards in Bengaluru:
Estimated Salary Range
- Entry-Level Professionals: ₹4.5 LPA – ₹7 LPA
- Experienced Candidates: ₹7 LPA – ₹10 LPA
Actual compensation may vary depending on experience, technical expertise, qualifications, and interview performance.
Employee Benefits
Employees joining Quanticate may receive:
- Competitive Salary Package
- Medical Insurance Coverage
- Family Health Benefits
- Accidental Insurance
- Flexible Working Hours
- Annual Leave Benefits
- Sick Leave Benefits
- Casual Leave Benefits
- Gratuity Benefits
- Professional Development Programs
- Coaching and Mentoring Support
- E-Learning Programs
- International Project Exposure
Interview Details
At the time of publication, Quanticate has not announced a specific interview date.
The selection process may include:
- Resume Screening
- Technical Assessment
- Clinical Data Management Interview
- HR Discussion
- Final Selection
Shortlisted candidates will be contacted directly by the recruitment team.
Required Documents
Candidates should keep the following documents ready:
- Updated Resume/CV
- Educational Certificates
- Degree Certificates
- Experience Certificates
- Government ID Proof
- Aadhaar Card
- PAN Card
- Passport-size Photograph
- Current Salary Details (if applicable)
- Notice Period Information (if applicable)
How to Apply
Interested and eligible candidates can apply through the official application link provided by Quanticate.
Candidates should ensure that their resume highlights:
- Clinical Data Management Experience
- EDC System Exposure
- Oracle Clinical Experience
- Medidata Rave Experience
- ICH-GCP Knowledge
- Query Management Activities
- Clinical Trial Experience
Applications should be submitted as early as possible.
Why Consider This Opportunity?
The Clinical Data Coordinator I position at Quanticate provides professionals with an opportunity to work on global clinical development programs while gaining hands-on experience in advanced clinical data management processes.
Professionals can build expertise in:
- Clinical Data Management
- Clinical Research
- Clinical Operations
- Pharmacovigilance
- Regulatory Affairs
- Biostatistics Support
- Global Clinical Trials
This exposure can significantly improve long-term career growth prospects within the healthcare and life sciences industry.
Frequently Asked Questions (FAQs)
Q1. What is the job location for this role?
The position is based in Bengaluru, Karnataka, India.
Q2. What is the job title offered by Quanticate?
The company is hiring for the position of Clinical Data Coordinator I.
Q3. Which EDC systems are preferred?
Experience with Oracle Clinical, Medidata Rave, and Inform is preferred.
Q4. Is knowledge of ICH-GCP required?
Yes. Knowledge of ICH-GCP guidelines is highly desirable.
Q5. What career paths can follow this role?
Professionals can progress toward Clinical Data Analyst, Clinical Data Manager, Clinical Operations Specialist, Pharmacovigilance Associate, or Regulatory Affairs roles.
Q6. What is the estimated salary range?
The estimated salary may range between ₹4.5 LPA and ₹10 LPA depending on experience and qualifications.
Final Conclusion
Quanticate's Clinical Data Coordinator I recruitment offers an excellent opportunity for professionals looking to establish themselves in Clinical Data Management and Clinical Research. The role provides exposure to global clinical trials, advanced EDC systems, regulatory requirements, and international healthcare projects.
Candidates with strong analytical skills, attention to detail, and experience in Clinical Data Management should consider applying for this opportunity to accelerate their career growth within the pharmaceutical and biotechnology industry.
Disclaimer
The information provided in this article is based on the job notification released by the employer. Candidates are advised to verify all details independently before applying.
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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