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CDC II

By Admin · Clinical Data Management

BANGALORE (IN)HYBRIDPOSTED: 9/13/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services
ICON

ROLE OVERVIEW

Support clinical data management activities for clinical trials by maintaining eCRFs and validation specifications, reconciling clinical and third-party data, monitoring study metrics and resolving data issues. The role contributes to high-quality clinical data delivery within a global clinical research organisation.

ROLE DEFINITION & RESPONSIBILITIES

  • •Assist the Data Management Study Lead with maintenance of eCRF, Data Validation Specifications and Study Specific Procedures
  • •Manage clinical and third-party data reconciliation based on edit specifications and data review plans
  • •Track and communicate study and task metrics to clinical data scientists, project teams and functional management
  • •Address data-related questions and recommend potential solutions
  • •Identify root causes and systematically resolve data issues
Reporting Hierarchy: Reports to the relevant Clinical Data Management/Clinical Data Science leadership function; Works closely with Data Management Study Leads, clinical data scientists, project teams and functional management

* Role responsibilities and qualifications synthesized based on industry benchmark standards.

QUALIFICATIONS & REQUIREMENTS

REQUIRED QUALIFICATIONS

  • Bachelor's degree in a relevant field such as Life Sciences or Healthcare
  • Intermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry
  • Familiarity with clinical data management software and systems such as Medidata or Oracle RDC
  • Strong attention to detail
  • Excellent communication and cross-functional collaboration skills
  • Legal right to work in India

PREFERRED QUALIFICATIONS

  • •Knowledge of regulatory guidelines and standards such as ICH-GCP
  • •Experience with additional clinical data management platforms
  • •Experience in global clinical research environments

REQUIRED VERIFIED SKILLS

Clinical data management
eCRF
Data Validation Specifications
Study Specific Procedures
clinical data reconciliation
third-party data reconciliation
edit specifications
data review plans
clinical data metrics
data issue resolution
Medidata
Oracle RDC

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Bonus & Equity: Competitive base salary and performance related incentives
Benefits: Health and wellbeing programmes including medical, dental and vision coverage where applicable; retirement and pension plans; life assurance and disability coverage; employee assistance programmes; learning and development opportunities
The posting does not disclose a fixed salary range. It states that ICON provides a competitive base salary and performance-related incentives, so exact compensation should be confirmed during recruitment.

ORGANIZATION CONTEXT & CULTURE

ICON is a global healthcare intelligence and clinical research organisation focused on accelerating the development of new medicines and treatments for patients.

TEAM SIZE: 40,000+ employees
INDUSTRY: Contract Research Organization (CRO) / Clinical Research / Healthcare Services
Culture: Values-driven culture centred on integrity, collaboration, agility and inclusion, with emphasis on patient impact and high-quality clinical research.

EXPECTED CAREER ROADMAP

The role can progress toward senior clinical data management positions, Data Management Study Lead responsibilities, clinical data science leadership or broader clinical operations and project-management tracks.

APPLICATION ADVISORY

Emphasize clinical data management experience and hands-on exposure to eCRFs, validation specifications and data reconciliation; Highlight Medidata, Oracle RDC or similar systems; Demonstrate root-cause analysis and data-query resolution skills; Mention ICH-GCP knowledge if applicable; Show strong attention to detail and cross-functional communication.
RECOMMENDED TRAINING
1/5
The Clinical Data Management Blueprint

The Clinical Data Management Blueprint

READY TO SUBMIT?

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