Provide administrative, clerical, implementation and/or processing support to the project teams and stakeholders. Assist with document/process/report development, testing, tracking, distribution, and management. Coordinate meetings, presentations, and training activities, facilitate billing and payment activities, and act as first
Job Description Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and
Job Specific Essential Duties & Responsibilities: Data Accuracy & Reporting Spend and cost savings data entry into StarCite meeting management tool. Quality control of final budgets for accuracy in spend and savings reporting. Enter final billing budget
Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The
Company Overview Docusign brings agreements to life. Over 1.5 million customers and more than a billion people in over 180 countries use Docusign solutions to accelerate the process of doing business and simplify people’s lives. With
Company Overview Docusign brings agreements to life. Over 1.5 million customers and more than a billion people in over 180 countries use Docusign solutions to accelerate the process of doing business and simplify people’s lives. With
We are seeking an Occupational Safety Technician to join our team. Based in Sorocaba, Brazil, you will be responsible for identifying, assessing, and controlling risks, while promoting the prevention of accidents and occupational illnesses. You will
Role Overview and Responsibilities We are seeking an Occupational Safety Analyst to join our team. Based in Sorocaba, Brazil, you will be responsible for providing operational, documentation, and organizational support for Health, Safety, and Environment (HSE)
Requisition ID: 98968 Job Category: Administration/Support Location: Belo Horizonte, Minas Gerais, Brazil Join a company that is passionately committed to the pursuit of a better world through positive change. With more than 70 years of business
Description : FIFA has established a Local FIFA Subsidiary in Brazil to work together with FIFA Zurich to deliver the biggest women’s sporting event in the world, the FIFA Women’s World Cup 2027 (“FWWC2027”) that for
Company Overview Docusign brings agreements to life. Over 1.5 million customers and more than a billion people in over 180 countries use Docusign solutions to accelerate the process of doing business and simplify people’s lives. With
tendersglobal.Net JOB DESCRIPTION IMPORTANT NOTICE: Please note that the deadline for receipt of applications indicated above reflects your personal device’s system settings. OBJECTIVE OF THE OFFICE The Noncommunicable Diseases and Mental Health (NMH) Department promotes, coordinates,
_Location: São Paulo _ - _Part-time: 20 hours per week on average _ - _Monthly base salary: R$5,208/month (2025 Monthly Compensation: R$5,466/month) _ - _Check out our values-driven benefits below! _ - Join us at Vera
Invoicing Administrator : Wärtsilä is an innovative technology company known for being a forerunner in the Marine and Energy markets. Every day, we - Wärtsilians - put our hearts and minds into turning Wärtsiläs purpose of
At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the worlds top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years
The Associate Project Manager, Early Phase and Translational Research (APM, EPTR) ensures the successful initiation, planning, execution, monitoring, controlling and closure of assigned Early Phase clinical research projects. In addition, the APM, EPTR is responsible for
O que buscamos: Complete higher education in Pharmacy, Biomedicine, or Nursing; Good Practices in Clinical Research, Initiation Visit, Routine, Close Out, and center qualification; Intermediate English; Minimum of 2 years experience in clinical research as a