Quanticate, a world-leading data-focused Contract Research Organization (CRO), is hiring a Data Process Associate in Bengaluru, Karnataka. This full-time, on-site opportunity is ideal for Life Sciences postgraduates looking to build a strong career in Clinical Data Management (CDM) and clinical research operations.
This role offers hands-on exposure to clinical trials data processing, regulatory-compliant workflows, and industry-standard Electronic Data Capture (EDC) systems. With a structured six-month intensive training program, Quanticate provides an excellent entry point into the global clinical research industry.
Job Overview
- Job Title: Data Process Associate
- Company: Quanticate
- Location: Bengaluru, Karnataka
- Employment Type: Full-time
- Work Mode: On-site
- Industry: Clinical Research / Clinical Data Management
- Annual Salary: ₹2.5 – ₹3.5 LPA (Estimated)
Key Responsibilities
As a Data Process Associate at Quanticate, your responsibilities will include:
- Accurate entry and verification of clinical trial data from Case Report Forms (CRFs) into study databases
- Performing quality control (QC) checks to ensure data accuracy and regulatory compliance
- Supporting database testing, documentation preparation, and clinical data processing activities
- Managing User Access for Electronic Data Capture (EDC) systems and maintaining audit-ready records
- Collaborating with project managers and cross-functional clinical teams
- Performing medical coding and other data management tasks as required
- Identifying process improvement opportunities to enhance data quality standards
Eligibility & Qualifications
Educational Requirements
- Master’s degree in Life Sciences or a related discipline
Required Skills & Knowledge
- Basic understanding of Clinical Data Management
- Knowledge of ICH-GCP guidelines and regulatory requirements related to data handling
- Proficiency in MS Excel and MS Word
- Strong analytical skills with high attention to detail
- Good written and verbal communication skills
- Ability to manage multiple priorities in a dynamic environment
- Team-oriented mindset with the ability to collaborate effectively
What You Will Gain
- Practical experience in regulated clinical research environments
- Exposure to global clinical trials and cross-functional project teams
- Strong foundation in clinical data standards, GCP, and regulatory compliance
- Skill development using industry-leading clinical data systems
- Long-term career growth opportunities in clinical data management and biostatistics
Benefits & Perks
- Competitive annual salary package
- Six-month intensive training plan
- Flexible working hours
- Paid leaves (Annual, Sick, Casual, and Bank Holidays)
- Medical insurance for self and immediate family
- Gratuity benefits
- Accidental insurance coverage
- Continuous learning through mentoring, coaching, e-learning, and job shadowing
About Quanticate
Quanticate is a globally recognized CRO specializing in clinical data management, biostatistics, and statistical programming. The company partners with top pharmaceutical organizations as well as emerging biotech firms to deliver high-quality, compliant clinical trial data solutions.
Quanticate strongly supports career development, offering professional society memberships and opportunities to work on complex, impactful clinical programs that contribute to advancing global healthcare.
How to Apply
