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If you’re passionate about clinical data management jobs in India and want to contribute to advancing healthcare, Quanticate is hiring a Data Process Associate in Bengaluru. This role offers intensive training, hands-on exposure to clinical research projects, and a solid career path in the pharmaceutical and CRO industry.
By joining Quanticate, a leading global data-focused CRO, you will gain in-depth knowledge of ICH-GCP guidelines, work with advanced EDC systems, and collaborate with international clinical research teams.
📝 Key Responsibilities
As a Data Process Associate, you will:
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- Enter and verify clinical data from Case Report Forms (CRFs) into study databases.
- Perform quality control checks for accuracy and compliance with GCP and ICH guidelines.
- Assist in database testing, documentation, and data processing across multiple projects.
- Support User Access Management for EDC systems.
- Collaborate with cross-functional teams to meet project deadlines.
- Contribute to medical coding and study-related tasks.
- Identify opportunities to improve data management processes.
🎓 Qualifications & Requirements
- Master’s degree in Life Sciences (M.Pharm, M.Sc., Biotechnology, Pharm.D.).
- Basic knowledge of Clinical Data Management processes.
- Familiarity with ICH-GCP guidelines and regulatory requirements.
- Strong PC skills (MS Word, Excel).
- Good analytical ability and attention to detail.
- Effective communication skills (oral and written).
- Ability to manage multiple priorities in a fast-paced environment.
💼 Benefits of Joining Quanticate
- Competitive salary package.
- Flexible working hours.
- Annual leave, sick leave, and bank holidays.
- Medical insurance for self and family.
- Accidental coverage & gratuity.
- Continuous learning: mentoring, coaching, e-learning, and job shadowing.
📌 How to Apply
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