Clinical Data Manager III
Location: Chennai, Tamil Nadu, India
Work Mode: Hybrid (On-site presence required)
Industry: Clinical Trial Organization (CTO)
Employment Type: Full time
Job Description:
Allucent™ is seeking an experienced Clinical Data Manager III to join our high-performing A-team. In this role, you’ll manage and coordinate data management deliverables across the clinical trial lifecycle—from database design and setup to final lock—ensuring data integrity, regulatory compliance, and timely delivery.
Key Responsibilities:
Act as the primary DM contact for internal teams (Clinical Programming, Biostatistics, Project Management, etc.) and external partners (sponsors, vendors, sites).
Lead planning and resource projection including task timelines, risk management, and scope changes.
Monitor project budgets and initiate changes when necessary.
Develop and maintain all DM project-specific documentation: DMPs, eCRF specifications, DVPs, and data transfer agreements.
Lead the database design and validation process, including eCRF design and user testing (UAT).
Review protocols, statistical plans, safety documents, and coordinate eCRF development.
Train EDC users with project-specific materials and ensure consistency in data review and cleaning.
Define data cleaning strategies and oversee all data releases including interim analyses and final database lock.
Reconcile data with external sources (SAE, PK, lab data, etc.).
Track project metrics, data trends, and compliance issues; share updates with Lead DM.
Conduct quality reviews and lead related activities.
Support vendor contract negotiations (EDC, IRT, eCOA).
Manage study close-out documentation and audit readiness.
Participate in internal audits and ensure ongoing documentation compliance.
Promote best practices and data standards (preferably CDISC STDM).
Drive initiatives to improve operational efficiency across studies.
Required Qualifications:
Bachelor’s degree in life sciences or equivalent qualification.
6+ years of experience in clinical data management (CRO, Pharma, or Biotech).
Strong understanding of CDM processes and systems, including EDC platforms.
Working knowledge of Microsoft Word and Excel.
Effective communication and interpersonal skills.
Demonstrated skills in problem-solving, time management, and adaptability.
Global team collaboration experience.
Awareness of ICH-GCP and regulatory standards.
Knowledge of Trial Master File and documentation standards.
Familiarity with data standards (CDISC STDM preferred).
Compensation:
Estimated salary range: ₹12 LPA – ₹18 LPA (based on experience and industry standards in Chennai)
Benefits:
Comprehensive location-specific benefits
Competitive salary
Dedicated training/study budget
Flexible working hours
Career mentoring and internal promotion opportunities
Access to e-learning (GoodHabitz & internal platforms)
Spot Bonus Award Program
Loyalty Award Program
Employee referral incentives
Inclusion in Allucent’s Buddy Program
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