Summary of Responsibilities: Follow all applicable departmental Standard Operating Procedures and Work Instructions. Complete day to day tasks ensuring quality and productivity. Execute high quality, timely monitoring and reporting plan(s) including specialized monitoring requests for approved protocols. Track and report…
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 process expeditable…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
We are seeking a highly skilled Workday PSA (Professional Services Automation) Architect to join our dynamic IT team. The ideal candidate will have extensive experience in Workday PSA and how to successfully deliver the solution within the challenges of the…
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 process expeditable…
Summary of Responsibilities: Respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. (Language of communication: French) 24x7 rotational shifts Receive information, record, and report Adverse Drug Reaction in timelines (according…
Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from…
Job Overview: 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. As a market leader in central laboratory and pre clinical…
Job Overview: 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. As a market leader in central laboratory and pre clinical…
Job Overview: It is the responsibility of the postholder to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost effective manner. They will be expected to comply with the legal requirements…
ob Overview: Prepares and negotiates and assists in the execution and retention of site agreements, confidentiality agreements, letters of indemnification and other contracts for Sponsors who contract Fortrea to perform this service. Maintains and contributes to contracts tracking and status…
Summary of Responsibilities: Act as the primary point of contact for global mobility and U.S. immigration matters. Manage all aspects of U.S. immigration compliance, including visa applications, renewals, and tracking expirations. Develop and maintain global mobility policies and processes, ensuring…
Job Overview: It is the responsibility of the post holder to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost effective manner. The individual will be expected to comply with the…
Job Overview: Manages ARC review and are responsible for performing TMF review of electronic Trial Master Files (eTMF), Trial, Country, and Site artifacts for clinical studies in support of sponsors services contracts and internal business needs. Summary of Responsibilities: Position…
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 process expeditable…
Job Overview: Responsible for assisting with 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 process…
Job Overview: The Workflow Analyst will hold the responsibilities of performing drug safety and pharmacovigilance support activities as assigned. Summary of Responsibilities: Segregate cases received as per priority and due dates in the database worklist. Assign cases to case processing…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Summary of Responsibilities: Respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. (Language of communication: French) 24x7 rotational shifts Receive information, record, and report Adverse Drug Reaction in timelines (according…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
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 process expeditable…
Job Overview: Responsible for the preparation and review of aggregate safety, risk management, and signal detection documents. Perform report management activities and lead client communication for the assigned reports. Assist other medical writers in their safety deliverables, act as a…
Job Overview: Responsible to provide analytical support for the developmental projects/comparative dissolution projects received from other client sites. Summary of Responsibilities: These statements are intended to describe the general nature of the job and are not intended to be an…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: The Senior Medical Reviewer provides medical input and medical review of moderate to complex clinical documents as Manuscripts. Abstracts, Posters, Advisory Board Meeting (ABM) reports, CSRs, Clinical and Nonclinical Overviews, Clinical and Nonclinical Summaries, IBs, Protocols, Product Monographs,…
At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an apprenticeship—it’s a launchpad for your future. As an Apprentice you’ll join a global team where curiosity, motivation, and fresh ideas are…
Apprenticeship Summary: 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) Assist and Support the Centralized Delivery Team in delivering for Global Clinical Operations and…
At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an apprenticeship—it’s a launchpad for your future. As an Apprentice you’ll join a global team where curiosity, motivation, and fresh ideas are…
Job Overview: Perform various project management and regulatory affairs activities for Fortrea clients.Manage team including performance reviews, human resource issues, and assist Senior Management in assigning resources to projects as required.Manage, coordinate and oversee the overall Regulatory Operations associated with…
Job Overview: The Card Services Supervisor leads a team through an outsourcing provider, to support Out of pocket , corporate credit card and P Card programs. This role requires independent decision making, initiative, and the ability to manage multiple priorities…
The AP Senior Manager is responsible for overseeing the end to end accounts payable process, with a focus on managing the relationship and performance of an outsourced service provider. This role ensures operational excellence, compliance, and continuous improvement through a…
Assists Proposal Managers with all aspects of the appropriate proposal process (text, quote, budget, and/or response to Requests for Information [RFIs]) (i.e., collating data, following up with other departments, meeting minutes, etc.). Responsible for managing opportunities of low complexity, with…
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 process expeditable…
Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and process expendable adverse…
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 process expeditable…
Job Overview: The Payroll Coordinator will provide full functional payroll support for the allocated APAC payrolls, although primarily home country, ensuring they are processed accurately and on time. They will ensure processing, payments and reporting deadlines are met in a…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from…
Job Overview: Lead the preparation and review of aggregate safety, risk management, signal detection, and benefit risk evaluation reports. Be responsible for end to end report management, including planning, authoring, and managing review, approval, and submission steps, per project scope…
Job Overview: Investigator Grants Estimates Responsibilities: Responsible for developing accurate and comprehensive investigator grant estimates for clinical research studies for inclusion in the proposal budget. This role partners with strategy, physicians, operations/delivery, proposal teams etc. to prepare tailored investigator grant…
Job Overview: Senior manager data integration connects their technical passion and skills for integration solutions with communication and organizational management. They have a great understanding of integration concepts, technology and processes for data movement across and between organizations and can…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an apprenticeship—it’s a launchpad for your future. As an Apprentice you’ll join a global team where curiosity, motivation, and fresh ideas are…
Job Overview: Lead the preparation and review of aggregate safety, risk management, signal detection, and benefit risk evaluation reports. Be responsible for end to end report management, including planning, authoring, and managing review, approval, and submission steps, per project scope…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
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 process expeditable…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: The Medical Data Review Manager is an important member of the Global Medical Review Team and has responsibility for execution of key Medical Data Review Activities, such as: Collaborates with the study team to perform oversight on clinical…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tools like Medidata RAVE or Oracle Inform or Data/Report programming or Visual Analytics tools like Spotfire or Tableau. Develop/validate Custom/Complex SAS /…
India Apprentice Program: Exciting opportunity to be part of the Fortrea India Apprentice Program! As a Fortrea Apprentice, you will have the opportunity to support meaningful assignments that compliment an education in STEM+ Business and Healthcare disciplines, and are inspiring…
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 process expeditable…
At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an apprenticeship—it’s a launchpad for your future. As an Apprentice you’ll join a global team where curiosity, motivation, and fresh ideas are…
At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an apprenticeship, it’s a launchpad for your future. As an Apprentice – Assistant Programmer, you’ll join a global team where curiosity, motivation,…
Job Overview: Responsible for the preparation and review of aggregate safety, risk management, and signal detection documents. Perform report management activities and lead client communication for the assigned reports. Assist other medical writers in their safety deliverables, act as a…
Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from…
Job Overview: Responsible for the preparation and review of aggregate safety, risk management, and signal detection documents. Perform report management activities and lead client communication for the assigned reports. Assist other medical writers in their safety deliverables, act as a…
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 process expeditable…
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 process expeditable…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
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 process expeditable…
Job Overview: Responsible for the management of site grant and non grant payment activities globally. Responsible for line management of Grant team personnel: hiring, mentoring, performance management; ensuring understanding of project specific and grant payment policies and procedures for direct…
The Product Owner has a key role in providing data driven insights that inform product decisions. They work intimately with the product team, including developers, designers, and testers to help shape the product’s features and roadmap by conducting market and…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: Serve as a member of the project team with primary responsibility for clinical data review, query generation / resolution and reconciliation to support the delivery of clinical data according to client quality and integrity specifications, and project timelines…
Apprentice – SEO Experience Required: 0 1 year Location: Bangalore (office based) Department: Digital Marketing Team About the Role We are looking for an enthusiastic, motivated, and detail oriented SEO Apprentice to join our dynamic Digital Marketing team in Bangalore.…
Apprentice Website Designer Experience Required: 0 – 1 year Location: Bangalore (Office based) Department: Marketing & Digital Team About the Role We are seeking a Apprentice Website Designer to support the Marketing and Digital teams by executing small to mid…
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 process expeditable…
Job Overview: Responsible for the preparation and review of aggregate safety, risk management, and signal detection documents. Perform report management activities and lead client communication for the assigned reports. Assist other medical writers in their safety deliverables, act as a…
Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and process expendable adverse…
Summary of Responsibilities: Owns all aspects of the appropriate proposal process (text, quote, budget, and/or response to Requests for Information [RFIs]) for assigned opportunities (inclusive of managing opportunities under general supervision, establishing clear timelines, meeting client requirement, and suggesting solutions…
Job Overview:The Payroll Specialist will provide full functional payroll support for the allocated payrolls, ensuring they are processed accurately and on time. They will ensure statutory compliance within their assigned EMEA countries are being adhered to and provide updates of…
Job Overview: May support LDM with the review, maintenance and update of External Vendor data received from central vendor or local laboratories. Working to ensure departmental SOPs, guidelines and global standards are followed to maintain data integrity and ensure consistency…
Summary of Responsibilities: Respond to medical information queries (In French)/product quality complaints/general queries that may be received over the telephone call, email, fax etc. Receive information, record, and report Adverse Drug Reaction in timelines (according to the regulations and to…
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 process expeditable…
Job Overview: Providing programming and analysis support for Real World Evidence projects for Fortrea clients. Having good understanding of the various sources on Real World Data to be used in the analysis. Summary of Responsibilities: Provide programming support for analysis…
Job Overview: Responsible to provide analytical support for the developmental projects/comparative dissolution projects received from other client sites. Summary of Responsibilities: These statements are intended to describe the general nature of the job and are not intended to be an…
Job Overview: Responsible to provide support lab compliance activities. Summary of Responsibilities: These statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills, and duties as…
Summary of Responsibilities: Perform the role of the Lead Statistical Programmer. Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments and…
Job Overview: Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US, EU, Japan, and ROW health authorities and oversight of the same, as applicable. Summary of Responsibilities: These statements are intended to describe the general nature of…
Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: Manage and review expeditable adverse events, product quality complaints and medical information to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. It is the responsibility of the…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
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 process expeditable…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: The Payroll Manager will lead and manage all activities related to international payroll processing, reporting, SOX, audit, business projects and vendor management for all legal entities and countries across a Continental region or a Cluster of the region.…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from…
Summary of Responsibilities: Follow applicable departmental Standard Operating Procedures and Work Instructions. Complete required trainings according to required timelines. Complete day to day tasks ensuring quality and productivity. Administer controlled documents ensuring availability to the end user. Maintain inventory of…
Job Overview: Serve as a member of the project team with primary responsibility for clinical data review, query generation / resolution and reconciliation to support the delivery of clinical data according to client quality and integrity specifications, and project timelines…
Job Overview: Leading projects and project teams for providing programming and analysis support for Real World Evidence projects for Fortrea clients. Having good understanding of the various sources on Real World Data to be used in the analysis. Training and…
Summary of Responsibilities: ================================ These statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills, and duties. Responsible to provide analytical support for the developmental projects/comparative…
Job Overview: Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary of Responsibilities: Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling,…
Job Overview: Providing programming and analysis support for Real World Evidence projects for Fortrea clients. Having good understanding of the various sources on Real World Data to be used in the analysis. Summary of Responsibilities: Provide programming support for analysis…
Summary of Responsibilities: Lead complex studies such as NDA submissions or complex, multi protocol programs, potentially coordinating activities across multiple locations, providing statistical oversight, and attending relevant project meetings. Perform project management activities for identified projects including resource planning, timelines,…