Voiant Clinical is hiring experienced Data Manager II professionals for its Remote India team. This is an excellent opportunity for Clinical Data Management professionals with experience in clinical trial data programming, data validation, CDISC standards, Python, SAS, R, or STATA to work with a global clinical research organization.

If you have experience in clinical data management, data programming, data quality review, and regulatory compliance, this remote opportunity offers the chance to work on international clinical trials while collaborating with cross-functional global teams.

Job Overview

• Position: Data Manager II
• Company: Voiant Clinical
• Location: Remote – India
• Job Type: Full-Time
• Experience: 3+ Years
• Industry: Clinical Research / CRO
• Work Mode: Remote

Key Responsibilities

The selected candidate will be responsible for:

• Independently managing clinical data management activities for assigned studies.
• Developing and maintaining Data Transfer Specifications (DTS).
• Performing clinical data extraction, transformation, cleansing, and formatting.
• Executing data validation and quality control checks.
• Testing and verifying clinical data management deliverables before production.
• Serving as the primary data management contact for routine study activities.
• Collaborating with cross-functional teams for timely issue resolution.
• Ensuring compliance with GCP, GDPR, HIPAA, 21 CFR Part 11, Annex 11, and applicable regulatory requirements.
• Maintaining documentation according to SOPs, Work Instructions, and GxP guidelines.
• Supporting additional study-related data management activities.

Eligibility Criteria

Candidates should possess:

• Bachelor’s or Master’s degree in Statistics, Engineering, or equivalent.
• Minimum 3 years of industry experience in Clinical Data Programming.
• Strong programming knowledge in at least two of the following:
  • Python
  • SAS
  • R
  • STATA
• Experience working in Pharmaceutical or CRO environments.
• Understanding of:
  • Clinical Trial Research
  • CDISC/SDTM Standards
  • FDA Regulations
  • ICH-GCP Guidelines
  • GDPR
  • 21 CFR Part 11
• Excellent communication and organizational skills.
• Proficiency in Microsoft Excel and Word.

Preferred Skills

• Clinical Data Management
• Clinical Trial Data Validation
• Data Programming
• Data Quality Assurance
• Data Transfer Specifications (DTS)
• Clinical Database Validation
• Python Programming
• SAS Programming
• R Programming
• STATA
• CDISC
• SDTM
• GCP
• FDA Regulations
• GDPR
• Clinical Research

Why Join Voiant Clinical?

Working with Voiant Clinical offers professionals an opportunity to:

• Work remotely from anywhere in India.
• Participate in global clinical research projects.
• Gain exposure to international pharmaceutical and CRO studies.
• Enhance expertise in clinical data programming and validation.
• Collaborate with multidisciplinary global teams.
• Build a long-term career in Clinical Data Management.

How to Apply

Interested candidates can send their updated CV to:

Email: hr@voiantclinical.com

Ensure your resume highlights:

• Clinical Data Management experience
• Programming skills (Python, SAS, R, STATA)
• CDISC/SDTM knowledge
• Clinical trial experience
• Regulatory compliance expertise