Quanticate hiring Data Process Associate in Bengaluru
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Education
- Skills & Knowledge Requirements
- Experience
- Location & Salary
- Training & Career Development
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- Will training be provided?
- Does this role involve clinical data handling?
- What regulatory standards are followed?
- What is the career growth after this role?
- Job Summary Table
Quanticate hiring Data Process Associate in Bengaluru. MSc Life Sciences candidates eligible. Clinical data management role with training.
Quanticate is hiring Data Process Associates for its clinical data management operations in Bengaluru, Karnataka. This role is ideal for postgraduate life science candidates who want to begin or strengthen their careers in clinical research, clinical data management, and CRO operations. The position offers structured training, exposure to global clinical trials, and hands-on experience with regulated data environments that support drug development and patient safety.
Company Overview
Quanticate is a world-leading, data-focused Contract Research Organization (CRO) specializing in clinical data management, biostatistics, and statistical programming. The company partners with global pharmaceutical companies and emerging biotechnology firms to support complex clinical trials across multiple therapeutic areas.
Known for its scientific rigor and data-driven approach, Quanticate plays a critical role in ensuring clinical trial data quality, regulatory compliance, and timely study delivery. The organization strongly supports career development through structured training programs, mentoring, professional society memberships, and continuous learning opportunities.
Job Role & Responsibilities
As a Data Process Associate, you will contribute directly to the success of clinical trials by ensuring accurate, compliant, and high-quality clinical data processing. This role forms a strong foundation for long-term careers in clinical data management and clinical research operations.
Key Responsibilities
- Accurately enter and verify clinical trial data from Case Report Forms (CRFs) into study databases
- Perform quality control checks to ensure data integrity and compliance with regulatory standards
- Assist with database testing, documentation preparation, and clinical data processing across multiple studies
- Support user access management for Electronic Data Capture (EDC) systems and maintain related documentation
- Collaborate with project managers and cross-functional clinical teams to meet study timelines
- Identify process improvement opportunities and contribute to maintaining high-quality data standards
- Perform basic medical coding activities as required to support study completion
- Follow ICH guidelines, GCP requirements, and internal SOPs related to data handling and processing
This role directly supports regulatory submissions and ensures that clinical trial data is reliable, audit-ready, and compliant.
Eligibility / Qualifications
Required Education
Candidates must have completed one of the following:
MSc Life Sciences, MSc Biotechnology, MSc Clinical Research, MSc Pharmacology, MSc Biomedical Sciences
Skills & Knowledge Requirements
- Basic knowledge of Clinical Data Management concepts
- Understanding of ICH Guidelines and Good Clinical Practice (GCP)
- Strong analytical skills with high attention to detail
- Proficiency in MS Excel, MS Word, and basic PC applications
- Good written and verbal communication skills
- Ability to manage multiple priorities in a fast-paced environment
- Team-oriented mindset with the ability to collaborate across functions
Experience
- Freshers or early-career professionals with relevant academic exposure are eligible
Location & Salary
- Job Location: Bengaluru, Karnataka
- Work Model: On-site
- Employment Type: Full-time
- Reported Salary: Approximately ₹300,000 per year
Compensation may vary based on candidate qualifications and internal company policies.
Training & Career Development
Quanticate provides a structured six-month intensive training plan covering clinical data management processes, regulatory requirements, and industry-standard systems. Employees also gain access to mentoring, coaching, e-learning, and job shadowing opportunities to support long-term career growth.
This role offers a clear pathway into advanced positions such as Clinical Data Coordinator, Clinical Data Analyst, and Data Management Lead.
Application Process
Interested and eligible candidates can apply directly through the official job listing:
Apply Here: https://www.linkedin.com/jobs/view/4330573877/
Shortlisted candidates will be contacted by the Quanticate recruitment team for further evaluation.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
Yes. Freshers with a postgraduate life sciences background are eligible.
Will training be provided?
Yes. Quanticate offers a six-month intensive training plan.
Does this role involve clinical data handling?
Yes. The role involves CRF data entry, quality checks, and EDC system support.
What regulatory standards are followed?
The role follows ICH Guidelines, GCP, and clinical data handling regulations.
What is the career growth after this role?
Career progression includes roles in clinical data management, biostatistics support, and CRO project operations.
Job Summary Table
| Company | Quanticate |
|---|---|
| Vacancies | Data Process Associate |
| Required Education | MSc Life Sciences, Biotechnology, Clinical Research, Pharmacology, Biomedical Sciences |
| Experience | Fresher / Early Career |
To apply for this job please visit www.linkedin.com.
