
Fortrea Development India Jobs in India
49 jobs at Fortrea Development India in India
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We are seeking a Solutions Architect to design and guide end-to-end solutions across our Corporate Systems portfolio (Finance, HR, Procurement, Corporate Systems). · Partner with business and technology leaders to translate strategy and requirements into secure scalable architec ...
Bengaluru1 month ago
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Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period. · Undertake primary medical review of cases including medical assessment of the case for seriousness listedness/labeling causality adverse ...
Pune1 month ago
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Responsible for preparing grants forecasts for studies through the communications with study teams to understand budget and assumptions. · ...
Bengaluru1 month ago
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The Apprentice participates in and executes the entry level department functions (Designation of Apprentice) in accordance with Fortrea and/or sponsor Standard Operating Procedures (SOPs). · Data entry of safety data onto adverse event tracking systems. · Write patient narrative ...
Bengaluru1 week ago
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The Apprentice Finance IT SoD Compliance supports the Finance IT organization in maintaining and improving Segregation of Duties (SoD) controls across financial systems. This role is designed for an early career professional seeking hands on experience in IT controls, financial s ...
Bengaluru5 days ago
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The job holder will lead the preparation and review of aggregate safety reports for clients globally. · ...
Mumbai1 month ago
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Informatics at Fortrea is a high profile, high impact team that focuses on creating innovative data-driven solutions to improve the speed, cost, and quality of drug development. · Design and implement scalable data solutions supporting organizational architecture and strategy. · ...
Bengaluru3 weeks ago
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Job Overview: · Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process, which may include safety data collected from clinical trials and/or post marketing settings (i.e., unsolicited reports). Manage and ...
Pune8 hours ago
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The role is primary contact for investigative sites for site payments. Responsible for administering grant and non-grant payments in accordance with the site executed agreement. · Accountable for the overall payment management of assigned studies which includes initial communicat ...
Bengaluru1 month ago
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Serve as a member of the project team with primary responsibility for coordinating the clinical data review query generation / resolution and reconciliation activities to support the Data Management lead with the delivery of clinical data according to client quality and integrity ...
Bengaluru1 month ago
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The Centralized Study Specialist II is a pivotal member of a Project Team responsible for the execution of a Clinical Research Project. · ...
Bengaluru1 month ago
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The Safety Science Coordinator will assist with Clinical Safety and/or PSS operations associated with products including adverse events process. · ...
Pune3 weeks ago
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Job Overview: · Responsible for general maintenance and any required archival of documents produced by the CPS Project Management (PM) Team. Organizing, gathering, scanning, and filing of all applicable documents into appropriate electronic and/or paper copy locations, including ...
Bengaluru, Mumbai, Pune1 week ago
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Job Overview: · We are seeking an experienced Workday Configuration Analyst with deep expertise in Record-to-Report (R2R) modules. This senior-level individual contributor role will be responsible for designing, building, testing, and deploying Workday solutions that enable accur ...
Remote1 week ago
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Summary of Responsibilities: · Performs supervisory duties for Document Specialists (DSs) including, but not limited to, interviewing, hiring, training, developing, performance evaluation, intervention, discipline, and discharge. · Organizing, gathering, scanning, and filing of a ...
Bengaluru1 week ago
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Job Overview: · Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and pr ...
Pune8 hours ago
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The Reporting Analyst II is responsible for overseeing end-to-end financial reporting and management of clinical trial investigator and study site payment. · ...
Bengaluru1 month ago
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Exciting opportunity to be part of the Fortrea India Apprentice Program. · ...
Bengaluru2 weeks ago
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Job Overview: · Lead the preparation and review of aggregate safety, risk management, signal detection, and benefit-risk evaluation reports. Demonstrate the ability to independently manage the production of safety deliverables, including those involving complex data analyses or i ...
Mumbai1 week ago
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Provide all clients with appropriate quality of service in a safe and cost-effective manner. · ...
Pune3 weeks ago