Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Data Coordinator I

Fortrea
Fortrea
3+ years
preferred by company
Bangalore, India
1 May 12, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Clinical Data Coordinator I

Job Location: Bangalore, India
Job Type: Full-Time
Department: Clinical / Clinical Data Management
Work Mode: Office-Based / Hybrid / Remote as per business requirements
Shift: Flexible Shifts
Experience Required: 3+ Years
Freshers Eligible: No
Industry: Clinical Research / Biotechnology / Pharmaceuticals / Healthcare / Medical Devices

Job Overview

We are hiring a Clinical Data Coordinator I for a leading clinical research and life sciences organization in Bangalore. This role is ideal for professionals with experience in clinical data management, clinical trials, external vendor data handling, laboratory data review, and healthcare data quality assurance.

The selected candidate will be responsible for supporting clinical data operations by managing external laboratory and vendor data, reviewing discrepancies, ensuring protocol compliance, maintaining data integrity, and supporting study-level clinical data workflows.

This is an excellent opportunity for experienced professionals looking to grow in clinical data management, pharmaceutical research, biotech operations, and global clinical trial data coordination.

Key Responsibilities

  • Review, maintain, and manage external vendor and laboratory clinical data to ensure consistency, completeness, and protocol compliance.
  • Verify that electronic vendor data includes all protocol-required parameters and is mapped correctly to designated patient records and database fields.
  • Support development and maintenance of Data Transfer Agreements (DTA) and Data Transfer Specifications for vendor data exchange.
  • Review and resolve clinical data discrepancies, edit check queries, and validation issues through structured query management processes.
  • Assist in validation review of electronically transmitted data samples before system loading.
  • Review external data edit checks, status reports, and study-specific clinical data listings.
  • Coordinate with Clinical Trial Managers (CTM), Clinical Research Associates (CRA), and internal clinical teams to obtain and verify local laboratory normal ranges.
  • Investigate discrepancies in laboratory reference ranges and maintain accurate supporting documentation.
  • Perform data entry and quality control checks for local laboratory normal range information.
  • Ensure laboratory normal ranges are correctly linked to patient test results within clinical databases.
  • Communicate vendor data transfer issues, data inconsistencies, and validation concerns to internal stakeholders and vendor teams.
  • Support broader clinical data management activities and operational projects as assigned.
  • Maintain confidentiality, regulatory compliance, and data security standards across all clinical operations.

Required Qualifications

  • Bachelor’s degree or university qualification in:
    • Life Sciences
    • Health Sciences
    • Biotechnology
    • Pharmacy
    • Clinical Research
    • Information Technology
    • Related scientific disciplines
  • Equivalent relevant professional experience may be considered in place of formal education.
  • Strong English communication skills (written and verbal).

Experience Requirements

  • Minimum 3+ years of experience in clinical research, pharmaceutical operations, biotechnology, clinical data management, medical devices, or diagnostics
  • Freshers are not eligible
  • Experience with clinical trial data handling and external vendor data management is highly preferred

Required Skills

  • Clinical Data Management
  • Clinical Trial Data Review
  • External Vendor Data Handling
  • Query Management
  • Data Validation
  • Laboratory Data Management
  • Clinical Database Review
  • Data Quality Assurance
  • Medical Terminology
  • Protocol Compliance
  • Clinical Documentation Review
  • Data Integrity Management
  • Stakeholder Communication

Preferred Knowledge

  • Understanding of ICH-GCP guidelines
  • Knowledge of clinical trial processes and healthcare regulatory compliance
  • Familiarity with clinical data transfer standards and vendor data reconciliation
  • Basic understanding of medical terminology