Join to apply for the workday financials architect role at fortrea 4 days ago be among the first 25 applicants join to apply for the workday financials architect role at fortrea get ai-powered advice on this job and more exclusive features. we are seeking a highly skilled workday fins (financials) architect to join our dynamic it team. the ideal candidate will have extensive experience in workday financials and how to successfully deliver the solution within the challenges of the cro environment. as a workday fins architect, you will be responsible for managing, optimizing, and strengthening our workday psa solutions to support our finance and operational needs which spans core accounting, banking and settlements, procurement, suppliers, and tax. remote based role in canada, india, mexico or united kingdom. summary of responsibilities lead the day-to-day management of the workday financials solutions. collaborate with cross-functional teams within operations and finance to gather requirements and translate them into effective workday financial configurations. align with workday psa and hcm architects to plan and deliver a roadmap aligned with enterprise leadership. continuously evaluate and optimize workday financials processes and configurations to enhance efficiency and user experience. understand workday financials product releases and oversee system regression testing. manage workday financials related projects, including planning, execution, monitoring, and reporting. support training and change management activities to maximize the effectiveness of the...
Recommended: - university/college degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology) and 2 years work experience in clinical research, including a strong working knowledge of the ich guidelines and fda, irb/iec regulations. minimum required: minimum 2 years of experience in clinical development or regulatory process. working knowledge of ich, fda, irb/iec, and other applicable regulations/guidelines; familiarity with investigator start-up documents and contract/budgets negotiation process; previous interaction with operational project teams and investigative sites - demonstrated understanding of research protocol requirements and proven ability to communicate with/educate others about them fortrea is proud to be an equal opportunity employer: as an eoe/aa employer, fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. we make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. we encourage all to apply. for more inform...
As a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. as a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. we are seeking a dedicated sr centralized study associate to join our team. the successful candidate will be responsible for: clinical systems & access management: managing clinical systems and access.maintaining study databases (ctms, iwrs, edc, etc.).supporting the study team in data review and other related activities.tracking and following up with cras for outstanding issues.generating study-specific reports.managing internal/external communications.assisting in ensuring training compliance for study teams.managing study payments (site and vendor). data review: following up with cras...
As a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. as a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. we are seeking an experienced and highly motivated centralized study specialist i to join our team. this role involves managing clinical systems, supporting study documentation, ensuring compliance, and providing leadership and mentorship to junior team members. the successful candidate will play a pivotal role in the successful execution of clinical trials and contribute to process improvement initiatives. key responsibilities: clinical systems management: oversee and manage clinical systems.maintain study databases (ctms, iwrs, edc, etc.).support etmf management. study coordination: tr...
As a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. as a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. we are seeking an experienced and highly motivated senior centralized study specialist to join our team. this role involves managing clinical systems, supporting study documentation, ensuring compliance, and providing leadership and mentorship to junior team members. the successful candidate will play a pivotal role in the successful execution of clinical trials and contribute to process improvement initiatives. key responsibilities: clinical systems management: manage clinical systems, including ctms milestone updates at site/country/protocol levels.manage and review study documents and...
As a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. fortrea is proud to be an equal opportunity employer: as an eoe/aa employer, fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. we make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. we encourage all to apply. for more information about how we collect and store your personal data, please see our privacy statement ....
As a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. **did you know?** **job summary**: the in-house clinical research associate (ihcra i) is an essential member of a clinical project team responsible for the execution of a clinical research project. the degree of responsibility given to the ihcra i shall reflect their experience, and level of contribution which they can make to the project. the work will involve clinical operations activities which will be conducted in an office or home based setting for designated projects as well as some travel to conduct site visits or to attend client or internal team meetings as needed. the ihcra i will be responsible for assisting with ensuring quality and integrity of data, and additional study related activities to support the efforts of study team members. activities will be conducted in compliance with company or sponsor sop, regulatory standards and applicable guidelines **experience** minimum required: - at least one year of experience in a related field, (e.g. medical, clinical, pharmaceutical, laboratory research, data analysis, data management or technical writing). one ye...
Cree una alerta de empleo y reciba nuevas ofertas que se adaptan a su perfil desde más de 2550 sitios web de empleo