Precision Medicine Group Hiring Clinical Data Associate II
Are you seeking Precision Medicine Group Careers, a Clinical Data Associate Job, or preclinical research validation vacancies in Bangalore? Leading clinical development services provider Precision Medicine Group has opened applications for the position of Clinical Data Associate II at its Bangalore office.
This clinical data review, database build validation, user acceptance testing (UAT), CRF specification design, and GCP compliance auditing vacancy operates under a full-time office model based in Bangalore, Karnataka, India. The position is open to life sciences, biology, or pharmacy graduates holding B.Pharm, M.Pharm, Pharm.D, B.Sc, or M.Sc degrees. Candidates must possess 2 to 4 years of clinical data management (CDM) experience. The data associate will assist Lead Data Managers on study startup, execute database testing, write validation checks, perform medical coding (MedDRA/WHODrug), and reconcile serious adverse event (SAE) logs. To build a corporate clinical resume detailing your database validation tests, EDC tools, or query management experience, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Overview
- Company: Precision Medicine Group
- Position: Clinical Data Associate II
- Job Location: Bangalore, Karnataka, India
- Employment Type: Full-Time
- Experience: 2 – 4 Years in Clinical Data Management (CDM)
- Qualifications: Bachelor's Degree / B.Pharm / M.Pharm / Pharm.D / BSc / MSc Life Sciences
- Expected Salary: ₹7,50,000 – ₹11,50,000 per annum (CTC Estimate)
💼 Key Responsibilities
- UAT Testing: Conduct user acceptance testing (UAT) for clinical databases and maintain validation documentation.
- CRF Development: Develop Case Report Form (CRF) design specifications from clinical protocols under direct supervision.
- Data Cleaning: Review, validate, and query clinical trial data inside Electronic Data Capture (EDC) systems.
- Medical Coding: Code clinical events, medical terms, and drug records using standardized dictionaries (MedDRA/WHODrug).
- SAE Reconciliation: Support coordination of serious adverse event (SAE) log reconciliations with safety databases.
- Reporting: Run patient-level database summaries, study status metrics, and discrepancy status reports.
To learn how clinical data associate salaries compare to pharmacovigilance safety case processor and preclinical toxicologist tracks, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Bachelor's degree or higher in a relevant scientific or life sciences discipline (B.Pharm/M.Pharm/PhD).
- Experience: 2 to 4 years of clinical data management (CDM) experience inside a CRO or pharma team.
- EDC Systems: Practical familiarity with leading Electronic Data Capture (EDC) systems.
- Office Tools: High proficiency in Microsoft Word, Excel, PowerPoint, and Outlook.
- Standards Knowledge: General knowledge of Good Clinical Practice (GCP) guidelines and trial documents.
For science postgraduates evaluating clinical data management and biostatistics careers compared to conventional quality control or formulation tracks, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Precision Medicine Group?
- Work for a global leader supporting advanced clinical trials for precision therapies.
- Obtain exposure to complex database builds, CRF design, and validation workflows.
- Excellent career growth pathways into Lead Data Manager or clinical project manager roles.
- Stable professional career with international biopharma client exposure.
To test your basic knowledge of drug safety regulations, site protocols, and GCP guidelines before your screening assessments, try our interactive Clinical Research Associate (CRA) Quiz.
💡 Clinical Data Associate vs Healthcare IT
Precision CDA Associates clean trial databases, run edit check validation logs, and perform medical coding, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Precision Medicine Candidates
- Detail UAT Skills: Specify database testing protocols and user acceptance test scripts you executed.
- Highlight Dicts Used: Mention MedDRA and WHODrug medical coding experience on your resume profile.
- Outline Specifications: Detail if you drafted CRF layout specifications or edit check definitions.
💬 Clinical Data Associate Interview Questions
- Q1. What is User Acceptance Testing (UAT) in Clinical Data Management?
Answer Guidance: UAT is a formal validation process where data managers test the newly built EDC database using test patient data to ensure all edit checks, layout screens, and query triggers function according to specifications. - Q2. How do you resolve inconsistencies during Serious Adverse Event (SAE) reconciliation?
Answer Guidance: I cross-reference clinical database parameters (like event description, onset date, severity) against the safety database logs, identify source differences, query the clinical site, and reconcile database entries once resolved. - Q3. What are Case Report Form (CRF) design specifications?
Answer Guidance: CRF design specifications are technical documents detailing the layout, fields, drop-down options, validation rules, and page routing of clinical forms built inside EDC systems based on protocol parameters.
📖 How to Apply?
Before submitting your application, please read the step-by-step guidance on how to navigate the registration portal, fill out required forms, and format your application profile:
📄 Premium ATS Resume Builder Service
Want to build a professional ATS-friendly resume tailored for Clinical Data Associate, database validation, or medical coding roles? Message us directly on our LinkedIn Company Page with the phrase "I want Resume Builder Service", and our expert team will connect with you:
📲 Message Us on LinkedIn🚀 Direct Application Links
If you are ready with your documents, submit your application directly via the official Precision careers portal:
Apply Online – Precision Careers (6115218004)❓ Frequently Asked Questions
Q. Is this Precision Medicine Group position remote?
No, this is an office-based, full-time position located at the Precision office in Bangalore.
Q. What is the required experience for this role?
Candidates should possess 2 to 4 years of active Clinical Data Management experience.
Q. Can science graduates apply?
Yes, candidates with a Bachelor's Degree in Life Sciences, Biology, Pharmacy, or equivalent discipline are eligible to apply.
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