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Clinical Data Manager Iii (India)

8+ years
₹12 LPA – ₹18 LPA
10 July 31, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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