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Clinical Data Manager

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Hybrid

Clinical Data Manager

Emmes Corporation

Clinical Data Manager

Skills

Google Cloud PlatformSQL QueriesOracleComplianceRisk Management

1 month ago

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Important information


Contract type:

Permanent

Salary:

₹1,000,000 – ₹1,200,000 / year

Location:

Bengaluru, Karnataka, India

Work mode:

Hybrid

Published on:

23 September 2026

What they need


Role & responsibilities

  • Develop and maintain data management plans DMPs, data validation specifications, and other study related documents.
  • Design and review CRFs eCRFs in collaboration with clinical teams and vendors.
  • Oversee the setup, validation, and ongoing maintenance of electronic data capture EDC systems, example, Medidata Rave, Oracle InForm, Veeva, REDCap.
  • Perform and review data cleaning, query generation, and issue resolution activities.
  • Ensure timely and accurate database lock and data delivery to biostatistics and other stakeholders.
  • Coordinate with CROs, EDC vendors, and central laboratories to ensure timely and compliant data activities.
  • Liaise with internal teams clinical, regulatory, biostats, safety to ensure alignment of data deliverables with study goals.
  • Participate in study team meetings and contribute to project timelines and risk management.
  • Ensure compliance with regulatory requirements, example, FDA 21 CFR Part 11, ICH GCP.
  • Conduct or support audits, data review meetings, and internal quality checks.
  • Maintain accurate and complete documentation for inspection readiness.
  • Performs other duties as assigned
  • Complies with all policies and standards

Preferred candidate profile

  • Bachelor's Degree Life Sciences, Health Information Management, Computer Science, or related field. Required
  • Master's Degree Life Sciences, Health Information Management, Computer Science, or related field. Preferred
  • 2- 4 years of experience in clinical data management (pharmaceutical, CRO, or biotech experience preferred). Required
  • 1-3 years Prior experience with EDC systems and CDISC standards (SDTM/ADaM) preferred. Preferred
  • Proficiency in EDC systems as Medidata Rave, Veeva, InForm. High
  • Familiarity with data standards as CDISC, MedDRA, WHODrug. High
  • Experience with database lock processes, query management, and edit checks. High
  • Knowledge of SAS, SQL, or other data handling languages is a plus. High
  • Strong attention to detail and organizational skills. High
  • Excellent communication and interpersonal abilities. High
  • Ability to manage multiple projects and deadlines. High
  • team oriented mindset with proactive problem solving skills. High

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