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Clinical Data Manager

Clario
CLARIO
1+ years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Job Title: Clinical Data Manager

Location: Bangalore, India | Remote (India)
Job Type: Full-Time
Posted: Yesterday
Job Requisition ID: R16967

About Us:
Clario is a global leader in clinical trial endpoint technology, dedicated to transforming evidence generation and improving patient outcomes. By leveraging advanced data management solutions across diverse therapeutic areas, Clario ensures clinical data accuracy, compliance, and quality throughout the lifecycle of sponsor clinical trials.

Role Overview:
We are seeking a Clinical Data Manager to manage and evaluate clinical data generated from imaging and other clinical trial sources. The role involves ensuring data integrity, resolving discrepancies, and collaborating with cross-functional teams to support high-quality trial execution.

Key Responsibilities:

  • Execute all data management deliverables for assigned studies.

  • Participate in client meetings and project discussions as required.

  • Understand study implementation requirements and data collection protocols.

  • Collaborate with project teams to design and review study-specific edit checks.

  • Define, run, and review edit checks; identify and resolve data discrepancies.

  • Maintain organized and up-to-date study documentation.

  • Perform study setup including trial framework (TF) design, database structure, and specifications.

  • Coordinate receipt and processing of electronic or ancillary data from external sources.

  • Track and follow up on outstanding issues until resolution.

  • Ensure compliance with regulatory guidelines and departmental SOPs.

  • Contribute to SOP updates and process improvements.

  • Maintain current knowledge of technical and industry trends in clinical data management.

Required Skills and Qualifications:

  • Education: Bachelor’s degree in Computer Science, Life Sciences, or related field (or equivalent experience).

  • Experience: Minimum 1 year in clinical data management within pharma, biotech, or CRO industry.

  • Working knowledge of relational databases; familiarity with SAS is desirable.

  • Proficiency in MS Word, Excel, and Access preferred.

  • Understanding of clinical trial terminology and processes.

  • Strong problem-solving skills with attention to detail.

  • Excellent interpersonal, communication, and documentation skills.

  • Ability to work independently and collaboratively in a team environment.

  • Flexible and adaptable to changing project priorities.

  • Based in India or able to work remotely/hybrid from India.

Why Join Clario:

  • Competitive compensation, incentives, and benefits including provident fund and medical insurance.

  • Flexible work environment with remote/hybrid options.

  • Opportunities for professional growth, training, and collaboration on global clinical trials.

  • Contribute to meaningful work that accelerates life-changing therapies for patients.

Learn more about Clario at clario.com.