Clinical Data Specialist Opening at Fortrea

Fortrea is hiring for the role of Clinical Data Specialist for its Bangalore office and remote work options. This opportunity is ideal for professionals with 3 to 5 years of relevant experience in Clinical Data Management (CDM) who have progressively handled increasing responsibilities in data management. The role is wellโ€‘suited for candidates with exposure to one or more therapeutic areas and a strong understanding of clinical trial data processes.

Clinical Data specialist

๐Ÿข Company Overview

Fortrea is a global clinical research organization providing comprehensive clinical development solutions to pharmaceutical, biotechnology, and medical device companies. Operating as a specialized CRO, Fortrea supports studies across multiple therapeutic areas and follows strict global regulatory and quality standards. Working at Fortrea offers professionals exposure to complex clinical trials, global datasets, and regulatoryโ€‘driven data environments.

๐Ÿ“Š Position Details

  • Position: Clinical Data Specialist
  • Department: CDM
  • Location: Banglore/remote
  • Experience: 3 to 5 Years
  • Qualification: B.Pharm, M.pharm, Degree in health scienece
  • Job Type: Full-Time

๐Ÿ“‹What You Will Doโ€“ Clinical Data specialist

As a Clinical Data Specialist, responsibilities may include:

  • Managing and reviewing clinical trial data across assigned studies
  • Performing data validation, discrepancy management, and data cleaning activities
  • Supporting database maintenance and data quality checks
  • Applying therapeutic area knowledge during data review
  • Ensuring data accuracy, consistency, and regulatory compliance
  • Supporting data deliverables for interim and final analyses
  • Collaborating with crossโ€‘functional teams including clinical, statistical, and operational groups
  • Following global SOPs, CDM standards, and regulatory guidelines

๐ŸŽ“ Who Can Apply

  • Candidates applying for this role should meet the following requirements:
  • Educational Background:
    • Degree in Health Sciences, Life Sciences, or a related discipline
  • Experience Requirement:
  • 3 to 5 years of relevant experience in Clinical Data Management
  • Progressive responsibility in data management activities
  • Experience supporting one or more therapeutic areas

๐Ÿง Skills Needed

  • The following skills are essential for success in this role:
  • Strong understanding of clinical data management processes
  • Experience with clinical trial databases and data workflows
  • Knowledge of at least one therapeutic area (multiโ€‘TA exposure is an advantage)
  • High attention to detail and data accuracy

โญWork Insight

The Clinical Data Specialist role is a key position in ensuring that clinical trial data is accurate, complete, and regulatoryโ€‘ready. Professionals at this level contribute significantly to trial quality by applying both technical CDM expertise and therapeutic knowledge. Working at Fortrea provides exposure to global studies, diverse therapeutic areas, and advanced data practices, making it a strong role for midโ€‘level CDM professionals aiming toward leadership positions.


๐ŸŽฏIdeal Candidates

This opportunity is suitable for:

  • Clinical Data Management professionals with 3โ€“5 years of experience
  • Candidates with therapeutic area knowledge
  • Individuals seeking remote or Bangaloreโ€‘based CDM roles
  • Professionals looking to grow in global CRO environments

๐Ÿ“ˆ Growth Opportunities

With experience and strong performance, professionals can progress into roles such as:

  • Senior Clinical Data Specialist
  • Clinical Data Lead
  • Data Quality or Data Operations Manager
  • Clinical Project Data Management roles

Fortrea supports continuous learning, advanced role exposure, and internal career mobility.


๐Ÿ’ฐ Expected Salary

  • Expected Salary: As per Fortrea company standards for midโ€‘level CDM roles

Compensation depends on experience, therapeutic expertise, and work location.


๐Ÿ’กApplication Tips

  • Revise CDM workflows including data cleaning and discrepancy management
  • Strengthen understanding of your therapeutic area(s)
  • Be prepared to discuss realโ€‘world data quality challenges
  • Highlight progressive responsibility and compliance experience in your resume

๐Ÿ”— Application Process

Interested candidates should apply only through the official company career website using the link provided below.

Important Disclaimer: This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.

Similar Job : Genectch research hiring for multiple role

๐Ÿ”— Explore Similar Opportunities

Pharmacovigilance Jobs for experienced

๐Ÿ“š Career Guide

Create a strong resume for pharma jobs

โ“FAQ

Q1. Is this role suitable for freshers?

No, this role requires 3โ€“5 years of relevant CDM experience.

Q2. Is remote work available?

Yes, this role offers Bangaloreโ€‘based and remote options.

Q3. Is therapeutic area experience mandatory?

Yes, knowledge of at least one therapeutic area is required.

Similar Posts