E
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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