Voiant Clinical Hiring Data Manager II (Remote India) | Clinical Data Management Career Opportunity
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Voiant Clinical Hiring Data Manager II (Remote India) |
Introduction
The clinical research industry continues to expand globally, creating significant demand for professionals skilled in Clinical Data Management, Clinical Data Programming, Data Validation, and Regulatory Compliance. Organizations conducting international clinical trials require experienced data management professionals who can ensure data quality, integrity, and compliance throughout the study lifecycle.
Voiant Clinical has announced a hiring opportunity for the position of Data Manager II for its Remote India team. This role is suitable for experienced professionals with expertise in clinical trial data management, CDISC standards, data programming, and quality control processes. Candidates who possess strong analytical skills and experience working in pharmaceutical companies or CRO environments can benefit from this opportunity.
If you are looking to build a long-term career in Clinical Data Management while working remotely on global clinical trials, this position may be an excellent fit.
About Voiant Clinical
Voiant Clinical is a global Clinical Research Organization (CRO) that provides specialized services in clinical trial management, clinical data management, biostatistics, regulatory support, pharmacovigilance, and medical writing.
The company supports pharmaceutical, biotechnology, and medical device organizations across multiple therapeutic areas. Through its global operations, Voiant Clinical assists sponsors in managing complex clinical development programs while ensuring regulatory compliance and high-quality data standards.
Company Overview
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Company Name: Voiant Clinical
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Industry: Clinical Research Organization (CRO)
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Headquarters: United States
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Business Focus: Clinical Research Services, Clinical Data Management, Biostatistics, Regulatory Support
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Global Presence: Multiple international clinical research projects
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Work Environment: Remote and Global Collaboration Model
Note: Employee count and establishment year may vary based on company updates and official disclosures.
Job Overview Summary
The Data Manager II role focuses on managing clinical trial data management activities across assigned studies. The selected candidate will be responsible for handling data extraction, validation, quality review, data programming, and regulatory-compliant documentation.
This position offers an opportunity to collaborate with international study teams while working remotely from India. Professionals with experience in CDISC standards, data validation techniques, and programming tools such as Python, SAS, R, or STATA are likely to find this role highly relevant.
Vacancy Details
| Particular | Details |
|---|
| Position | Data Manager II |
| Company | Voiant Clinical |
| Location | Remote – India |
| Job Type | Full-Time |
| Work Mode | Remote |
| Industry | Clinical Research / CRO |
| Experience | 3+ Years |
| Qualification | Bachelor's or Master's Degree |
| Department | Clinical Data Management |
Job Role Explanation
What Does a Data Manager II Do?
A Data Manager II plays a crucial role in ensuring that clinical trial data remains accurate, complete, consistent, and audit-ready throughout the study lifecycle.
The professional works closely with clinical operations teams, statisticians, programmers, and sponsors to manage data collection, validation, cleaning, reconciliation, and reporting activities.
In modern clinical research, data quality directly impacts regulatory submissions and study outcomes. Therefore, Data Managers serve as key contributors to successful clinical trials.
Key Responsibilities Explained
The selected candidate will perform a variety of clinical data management activities, including:
Clinical Data Management
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Independently manage assigned clinical studies.
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Monitor data collection processes.
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Ensure data accuracy and completeness.
Data Programming Activities
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Develop and maintain Data Transfer Specifications (DTS).
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Support data extraction and transformation processes.
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Generate quality datasets for analysis.
Data Validation and Quality Review
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Conduct data review and discrepancy identification.
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Execute validation checks.
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Ensure high-quality clinical databases.
Regulatory Compliance
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Follow GCP guidelines.
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Maintain compliance with:
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GDPR
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HIPAA
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FDA regulations
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21 CFR Part 11
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Annex 11 requirements
Documentation Management
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Maintain SOP-compliant documentation.
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Support audit readiness activities.
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Ensure proper study record management.
Cross-Functional Collaboration
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Coordinate with programmers, statisticians, clinical teams, and sponsors.
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Resolve data issues within required timelines.
Eligibility Criteria
Applicants should possess the following qualifications:
Educational Qualification
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Bachelor's Degree in Statistics, Engineering, or equivalent discipline
OR
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Master's Degree in Statistics, Engineering, or equivalent discipline
Experience Required
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Minimum 3 years of Clinical Data Programming experience
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Experience in Pharmaceutical or CRO environments
Knowledge Requirements
Candidates should have an understanding of:
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Clinical Trial Research
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Clinical Data Management
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CDISC Standards
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SDTM Standards
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FDA Regulations
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ICH-GCP Guidelines
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GDPR Compliance
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21 CFR Part 11
Skills Required
Successful candidates are expected to possess the following skills:
Technical Skills
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Clinical Data Management
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Clinical Data Validation
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Data Programming
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Data Quality Review
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Clinical Database Validation
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Data Transfer Specifications (DTS)
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CDISC
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SDTM
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Clinical Trial Data Processing
Programming Skills
Strong expertise in at least two of the following:
Software Skills
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Microsoft Excel
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Microsoft Word
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Clinical Data Management Systems
Soft Skills
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Analytical Thinking
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Problem Solving
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Communication Skills
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Attention to Detail
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Time Management
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Team Collaboration
Expected Salary
The company has not officially disclosed the salary package.
Based on similar Clinical Data Management and Clinical Data Programming roles in India:
Estimated Salary Range
₹8 LPA – ₹18 LPA
Compensation may vary depending on:
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Experience level
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Programming expertise
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CRO experience
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Clinical trial exposure
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Interview performance
Interview Process
Although the official recruitment process has not been disclosed, candidates can generally expect:
Stage 1
Resume Screening
Stage 2
HR Discussion
Stage 3
Technical Interview
Topics may include:
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Clinical Data Management
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CDISC
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SDTM
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Data Validation
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SAS/Python/R/STATA
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Clinical Trial Concepts
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Regulatory Compliance
Stage 4
Final Managerial Round
Stage 5
Offer Release
Required Documents
Candidates should keep the following documents ready before applying:
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Updated Resume/CV
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Educational Certificates
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Degree Certificates
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Experience Letters
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Salary Slips (if applicable)
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Identity Proof
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Address Proof
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Professional Certifications
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Programming Certifications (if available)
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Clinical Research Training Certificates
Why Join Voiant Clinical?
Working at Voiant Clinical provides several career advantages:
Remote Working Opportunity
Work from anywhere in India.
Global Exposure
Contribute to international clinical research projects.
Technical Growth
Gain expertise in:
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Clinical Data Programming
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Data Validation
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CDISC Standards
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Regulatory Compliance
Career Advancement
Build a long-term career in Clinical Data Management and Clinical Research.
Collaborative Environment
Work alongside experienced global professionals and multidisciplinary teams.
How to Apply
Interested candidates can send their updated resume to:
Email: hr@voiantclinical.com
Application Tips
Ensure your resume highlights:
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Clinical Data Management Experience
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Clinical Trial Exposure
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CDISC and SDTM Knowledge
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Programming Skills (Python, SAS, R, STATA)
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Regulatory Compliance Expertise
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Data Validation Experience
Frequently Asked Questions (FAQs)
Is this a remote job?
Yes. This position is fully remote for candidates based in India.
What is the minimum experience required?
Candidates should have at least 3 years of Clinical Data Programming experience.
Which programming languages are preferred?
Python, SAS, R, and STATA are preferred. Knowledge of at least two is expected.
Is CRO experience mandatory?
While not explicitly mandatory, experience in pharmaceutical companies or CRO environments is preferred.
What qualifications are accepted?
Bachelor's or Master's Degree in Statistics, Engineering, or equivalent disciplines.
Is CDISC knowledge required?
Yes. Understanding of CDISC and SDTM standards is one of the key requirements.
Final Conclusion
The Voiant Clinical Data Manager II opportunity is an excellent option for experienced Clinical Data Management professionals seeking remote pharmaceutical and clinical research jobs in India. The role combines clinical data programming, validation, regulatory compliance, and global clinical trial exposure, making it highly valuable for professionals looking to advance their careers within the CRO and pharmaceutical industry.
Candidates with strong programming expertise, knowledge of CDISC standards, and experience in clinical research data management should consider applying for this position to gain international exposure and long-term career growth opportunities.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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