Fortrea Clinical Data Specialist Opportunity in Bangalore

Fortrea Hiring Clinical Data Specialist in Bangalore

Fortrea, a leading global contract research organization (CRO), is seeking a highly skilled and motivated Clinical Data Specialist to join their team in Bangalore. With over 19,000 staff members conducting operations in more than 90 countries, Fortrea is dedicated to transforming drug and device development for partners and patients across the globe.

About Fortrea

Fortrea specializes in providing pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions. The company operates in over 20 therapeutic areas and is committed to scientific rigor and innovative clinical development practices.

Job Details

Position: Clinical Data Specialist
Location: Bangalore, India
Experience Required: 3-5 years in data management

Responsibilities

• Ensures that all allocated projects are carried out in strict accordance with the relevant
• protocols, global harmonized SOPs, and the specified standards of GCPs.
• Demonstrates capability to read and follow study timelines for on-time deliverables.
• Potential to assist with inputs on study design or capable to make suggestions to study timelines when warranted.
• Assist with review of clinical trial data in accordance with Data Management Plans and/or Data Review Guidelines and raise queries to resolve erroneous, missing, incomplete data.
• Run and execute additional programs (special listings, reconciliation discrepancy listings, etc.) used to support the review of clinical trial data.
• Generate, resolve and track queries to address problematic data identified during aggregate data review activities.
• Interacts with other project team members to support the set-up, maintenance, and closure of the Data Management aspects of the project and attend meetings as required.
• Generate and QCs data listings for internal data review.
• May assist or create dummy data to test edit checks and to test database screen design and functionality.
• Assist or create dummy data to test SAS reports and data listing.
• Demonstrates the ability to review Edit Check Specifications and Database
• specifications.
• Post Data Management documentation and data management related administrative tasks as requested, including maintenance of eTMF as required.
• Runs study status reports in preparation for Sponsor meetings and to deliver on specific sponsor request.
• Assist with the completion of Database Lock and Unlock activities.
• Supports the training of new staff on project specific Data Management processes.
• Performs any other duties as assigned.

Qualifications

• Education: University/college degree in life sciences, health sciences, information technology, or a related field, or certification in allied health professions from an accredited institution.
• Experience: 3-5 years of relevant work experience in data management, with knowledge of one or more therapeutic areas.
• Skills: Knowledge of effective clinical data management practices and medical terminology is preferred. Strong time management skills and the ability to adhere to project productivity metrics and timelines are essential.
• Language: Fluent in English, both written and verbal.

How to Apply

Interested candidates are encouraged to apply by visiting Fortrea’s career page and submitting resumes.

Tagged as: Global Pharma Jobs, Good Clinical Practice (GCP), Pharmaceutical Careers, Pharmaceutical Jobs