Clario
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Data Acquisition Associate – Data Management
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Clario is hiring a Data Acquisition Associate for its Bangalore operations. The role requires a minimum of 1 year of relevant experience in areas such as data processing, data coordination, clinical operations, healthcare administration, or related functions. The selected candidate will support the receipt, processing, review, tracking, and maintenance of clinical trial source data throughout the study lifecycle. Key responsibilities include data quality checks, query resolution, documentation management, data entry, and operational tracking. Candidates with backgrounds in Life Sciences, Healthcare, Clinical Research, Data Management, Business Administration, or related disciplines are relevant for this opportunity.
Job Overview
| Particulars | Details |
|---|---|
| Position | Data Acquisition Associate – Data Management |
| Company | Clario |
| Location | Bangalore |
| Job Type | Full-Time |
| Experience | 0 - 1 years |
| Category / Department | Pharma |
| Application Mode | Online |
🏢 About Clario
Company Overview:
Clario is a company operating in the clinical research, healthcare, and life sciences sector. The Data Acquisition Associate position is part of Clario’s Digital Physiology Solutions business and focuses on the accurate handling, processing, tracking, quality review, and maintenance of clinical trial source data.
Company Mission:
Not Provided
Company Vision:
Not Provided
Core Values / Principles
Data accuracy and quality
Compliance with established procedures
Operational efficiency
Continuous improvement
🌐
Company Website
📍
Office Location
Not Provided
💡 Editor's Note / Preparation Tip
Resume Tips:
Highlight experience in clinical data processing, data entry, data coordination, or healthcare operations.
Mention relevant qualifications such as B.Pharm, Pharm.D, B.Sc, B.Tech, BBA, BCA, M.Pharm, M.Sc, or MBA where applicable.
Clearly showcase experience with Excel, data validation, documentation, and quality checks.
Quantify relevant achievements involving data accuracy, productivity, or operational efficiency.
Use keywords such as Clinical Data Management, Data Acquisition, Data Quality, Clinical Research, Data Processing, Query Resolution, and Documentation.
Interview Preparation:
Revise the clinical trial data lifecycle and basic clinical data management concepts.
Prepare to explain how you identify and resolve data-quality issues.
Review Excel functions and common data-validation techniques.
Be ready to discuss documentation accuracy and handling confidential study information.
Prepare examples demonstrating attention to detail, time management, and problem-solving.
Professional Tips:
Ensure your resume accurately reflects your education and relevant experience.
Highlight regulated-industry or healthcare experience when applicable.
Review your application carefully for spelling, formatting, and data accuracy before submission.
Apply through the provided official application route.
📝 Job Description
Position Details:
The Data Acquisition Associate will support clinical trial operations by ensuring that clinical source data is accurately received, processed, reviewed, tracked, and maintained according to established procedures and quality requirements.
The position involves clinical data processing, data quality review, documentation management, query resolution, operational tracking, and coordination with cross-functional teams. The role also requires maintaining productivity and quality standards while completing assigned activities within defined timelines.
Benefits / Compensation
According to the supplied information, benefits may include:
Competitive compensation and incentives
Provident Fund
Medical insurance
Employee engagement programs and local events
Modern office facilities
Remote-work flexibility
Professional development opportunities
Career growth within a global organization
Candidate Requirements:
Minimum 1 year of relevant professional experience.
Bachelor’s degree in a relevant discipline.
Background in Life Sciences, Healthcare, Clinical Research, Data Management, Business Administration, or a related field.
Strong attention to detail and data accuracy.
Ability to manage documentation and assigned operational activities.
Good written and verbal English communication skills.
Ability to work independently and collaboratively.
Ability to learn and use new computer systems.
Preferred Skills:
Clinical data processing
Data coordination
Clinical operations
Data entry and review
Data quality checks
Documentation management
Query resolution
Microsoft Excel, Word, Outlook, and Teams
Analytical and problem-solving skills
Proofreading and organizational skills
Working Days & Hours:
Not Provided
How to Apply:
Apply through the provided Clario application link:
https://clarioclinical.wd1.myworkdayjobs.com/en-US/clarioclinical_careers/job/Bangalore-India/Data-Acquisition-Associate_R18065-2
🎯 Key Responsibilities
- ✓ Receive, review, and process clinical trial source data according to established procedures.
- ✓ Enter and maintain clinical study information in relevant operational systems.
- ✓ Review clinical data for completeness, accuracy, and quality.
- ✓ Perform data quality checks and support query resolution.
- ✓ Monitor assigned work queues and complete activities within required timelines.
- ✓ Maintain productivity and quality metrics.
- ✓ Organize and archive study documentation and source records.
- ✓ Monitor centralized mailboxes and route communications to appropriate teams.
- ✓ Track source-document retrieval requests and maintain movement logs.
- ✓ Support project teams with data entry, data review, and operational activities.
- ✓ Participate in Project Assurance meetings.
- ✓ Maintain study tracking and documentation.
- ✓ Identify and report system, equipment, or process issues.
- ✓ Follow required training and departmental quality procedures.
- ✓ Contribute to continuous improvement initiatives.
💡 Required Qualifications & Skills
✓ Clinical data processing and data entry
✓ Data quality review
✓ Attention to detail
✓ Documentation management
✓ Query resolution
✓ Analytical and problem-solving skills
✓ Organizational and time-management skills
✓ Microsoft Excel, Word, Outlook, and Teams
✓ Written and verbal English communication
✓ Ability to learn new computer systems
✓ Team collaboration
✓ Ability to work independently
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Data Acquisition Associate – Data Management role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Expected Career Progression Roadmap:
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
💡 Pro-Tip: Before your interview, research the company's recent news, product launches, and Glassdoor work reviews. Prepare 2-3 thoughtful questions for the interviewer regarding team dynamics and success metrics for this role.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated Market Compensation in India:
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Suggested Professional Certifications:
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
Frequently Asked Questions
What position is Clario hiring for?
Clario is hiring for a Data Acquisition Associate – Data Management position.
Where is the Data Acquisition Associate position located?
The position is based in Bangalore, India.
What is the minimum experience required?
The supplied information specifies a minimum of 1 year of relevant experience.
What educational qualification is required?
A Bachelor’s degree in Life Sciences, Healthcare, Clinical Research, Data Management, Business Administration, or a related field is preferred.
Can B.Pharm candidates apply?
Yes. B.Pharm is listed among the relevant qualifications for this opportunity.
Can Pharm.D candidates apply?
Yes. Pharm.D is included among the relevant educational backgrounds.
What type of work will the selected candidate perform?
The role involves clinical source data processing, data review, quality checks, documentation, query resolution, tracking, and operational support.
Is clinical research experience required?
The supplied information indicates that relevant experience in clinical research, healthcare, pharmaceutical services, data processing, or related regulated-industry operations is preferred.
What technical skills are useful for this position?
Candidates should be comfortable with Microsoft Excel, Word, Outlook, and Teams. Data entry, validation, documentation, and data quality skills are also important.
How can candidates apply for this position?
Candidates can apply through the provided Clario Workday application link.
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