Indero Senior Clinical Data Coder Remote

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Indero Recruitment – Senior Clinical Data Coder

Indero is inviting applications for the Senior Clinical Data Coder – India position on a permanent, full-time basis. This home-based opportunity is suitable for experienced professionals in clinical data coding, clinical trials, and pharmaceutical or contract research organization (CRO) environments. Candidates with at least five years of relevant experience, knowledge of MedDRA and WHO Drug dictionaries, and expertise in coding module setup can apply. The role involves clinical data coding, coding convention management, data review, query resolution, and coordination of coding activities across multiple studies.

Company Overview

Indero is a global contract research organization specializing in dermatology and rheumatology clinical research. Formerly known as Innovaderm, the company has more than two decades of clinical research experience and supports pharmaceutical and biotechnology sponsors through services spanning protocol design, patient recruitment, trial monitoring, and biometrics.

Indero emphasizes collaboration, innovation, reliability, and responsiveness, with opportunities for professional development and advancement.

Job Details

Particulars Details
Company Indero
Job Title Senior Clinical Data Coder
Job Location India
Work Mode Remote / Home-based
Employment Type Permanent, full-time
Experience Minimum 5 years of relevant experience
Job Category Clinical Data Management / Clinical Data Coding
Work Schedule Flexible schedule; some evening meetings required
Official Application Apply Online

Job Role & Responsibilities

The Senior Clinical Data Coder will lead and oversee clinical data coding activities across multiple ongoing studies, ensuring coding accuracy, regulatory compliance, and timely delivery of study requirements.

Key responsibilities include:

  • Code medical terms and medications accurately using MedDRA, WHO Drug, and internal coding conventions.

  • Oversee coding module setup for assigned studies and ensure appropriate configurations and workflows.

  • Define, document, and manage coding conventions to maintain consistency across studies.

  • Coordinate coding activities as the Lead Coder across multiple studies simultaneously.

  • Validate sponsor coding licenses.

  • Prioritize coding deliverables and balance workloads across studies and timelines.

  • Contribute to the coding sections of Data Management Plans.

  • Oversee and perform dictionary version upgrades and related activities.

  • Validate and test coding setups, coding report programming, and associated database checks.

  • Support clinical data review and resolve data clarifications within required timelines.

  • Mentor and guide junior or backup coders.

  • Contribute to process optimization, SOP development, and coding best practices.

  • Maintain effective communication with Data Management Leads, Clinical Research Associates (CRAs), and other stakeholders.

Eligibility & Qualifications

Candidates should possess a Bachelor’s degree or equivalent in Pharmacy, Life Sciences, or a related field. Medical or Nursing backgrounds are also acceptable.

Experience Requirements

  • Minimum 5 years of relevant clinical data coding experience in clinical trials or the pharmaceutical/CRO environment.

  • Demonstrated experience in coding module setup and coding convention management.

  • Experience prioritizing coding tasks across multiple clinical studies.

  • Experience in clinical data review and query management.

Required Skills & Competencies

Applicants should demonstrate the following skills and knowledge:

  • Thorough knowledge of medical terminology.

  • Working knowledge of MedDRA and WHO Drug medical dictionaries.

  • Experience with coding module configuration, validation, and dictionary upgrades.

  • Understanding of clinical data management workflows and coding-related database checks.

  • Strong organizational, analytical, and problem-solving skills.

  • High attention to detail and commitment to data accuracy.

  • Excellent written and verbal English communication skills.

  • Ability to lead and support colleagues in a global team environment.

  • Good knowledge of Good Clinical Practice (GCP).

  • Familiarity with applicable Health Canada, US FDA, and European Medicines Agency (EMA) regulations and guidelines.

Work Location & Benefits

This is a home-based position in India. Candidates should be legally eligible to work in India and willing to attend some meetings outside regular working hours, primarily in the evening.

Indero lists the following benefits:

  • Flexible work schedule.

  • Permanent, full-time employment.

  • Ongoing learning and development opportunities.

  • Opportunities for professional growth and advancement.

How to Apply

Interested and eligible candidates can submit their applications through the official Indero careers website.

Apply for Senior Clinical Data Coder – India

Applicants should review the official requirements and ensure they have the relevant clinical data coding experience, medical dictionary knowledge, and coding leadership capabilities.

Job Summary

Category Details
Company Indero
Vacancies (position titles) Senior Clinical Data Coder
Required Education Bachelor’s degree or equivalent in Pharmacy, Life Sciences, or a related field; Medical or Nursing background also acceptable
Experience Minimum 5 years of relevant clinical data coding experience in clinical trials or the pharmaceutical/CRO environment