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Coding Specialist I

Thepharmadaily
Bangalore8-13 LPA Posted 13 Aug 2025
FULL TIME
Biometrics
Data Management

Job Description

Key Responsibilities: Data Coding Project Support:

  • Perform Clinical Data Coding: Assist with the coding of clinical medical data on assigned projects, working with supervision.
  • Collaborate with Teams: Work closely with the Coding team and Lead Data Reviewer to address all coding aspects for projects, including start-up, maintenance, and completion phases.
  • Coding Status Liaison Support: Provide updates on coding status to project liaisons and assist in resolving any coding-related issues.

Project Process Management:

  • Data Management Plan Support: Assist in reviewing Data Management Plans, particularly coding-related sections, and Study-Specific Dictionary Coding Conventions.
  • Data Handling Quality: Support the setup, maintenance, and closure of data management processes for quality coding of clinical data.
  • Process Improvement: Contribute solutions for process and efficiency improvement on coding-related tasks and projects.

Training Development:

  • Professional Development: Participate in internal and external training seminars to maintain coding competencies.
  • Team Collaboration: Support project staff globally to ensure client satisfaction by delivering quality coded data on time and within budget.

Additional Responsibilities:

  • Dictionary Verification Support: Assist with dictionary verification tasks as needed.
  • Other Duties: Perform other duties as assigned, contributing to the overall success of the project and team.

Qualifications: Education Experience:

  • Required:
  • University/College degree in Life Sciences, Health Sciences, Information Technology, or a related field, or a certification in allied health professions from an accredited institution.
  • Fortrea may consider relevant equivalent experience in lieu of formal education.
  • Required Experience:
  • A minimum of 4 years of relevant experience in data management within a clinical trial setting.
  • Basic knowledge of medical coding processes and various coding tools (e.g., Medidata Coder, Central Coding).
  • Familiarity with clinical trial processes, data management, biometrics, and systems applications to support operations.

Skills:

  • Communication Skills: Excellent oral and written communication and presentation skills.
  • Interpersonal Skills: Strong interpersonal skills with the ability to work collaboratively in cross-functional teams.
  • Knowledge of Clinical Trials: Understanding of clinical trial processes, data management, and related activities.

What You Will Get:

  • Competitive Salary Benefits:
  • Health, Dental, and Vision insurance
  • Life insurance, Short-Term/Long-Term Disability (STD/LTD)
  • 401(K) retirement plan
  • Paid time off (PTO) or flexible time off (FTO)
  • Employee Stock Purchase Plan (ESPP)
  • Company bonus (where applicable)

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