Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so,
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the
Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the
Overview: Serve as Senior Data Coordinator for allocated complex studies and serve in a leadership role to a specific DM Task. Essential Functions: • Serve as a lead DM and the main point of contact for various projects
IQVIA Biotech is growing! Our team in Brazil has openings for Clinical Project Coordinators. This role can be home-based anywhere in Brazil. Job Overview Support, with minimal supervision, the Project Leader (PL) and Clinical Project Manager (CPM)
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of
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 Sr CRA
Position Overview ABOUT RARE Rare inspires change so people and nature thrive. Our culture is result-oriented and entrepreneurial, committed to ambitious goals and measurable results. The Marketing & Communications Associate works with teams across Rare Brazil
JOB DETAILS Type of contract : Service Contract Level : SC8 Hiring Unit : Culture Sector (CLT) Duty Station : Brasilia Work location : On site Duration of contract : 12 months Hiring open to :
Responsibilities include, but are not limited to : - The role is accountable for performance and compliance for assigned protocols and sites in a country; - Under the oversight of the CRA manager the person ensures
Job Summary: As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start up. You will be a productive member of the team,
When our values align, theres no limit to what we can achieve. An initiation Clinical Research Associate (i CRA) specializing in Pre SIV and Activation tasks will be assigned & accountable for managing and driving the
Job Overview: The Learning Support Teacher plays a crucial, integral role in ensuring high-quality learning support for students, serving as a key advocate and model for inclusive and equitable approaches to education. This position requires a
Job Summary: As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start up. You will be a productive member of the team,
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,
The Senior Project Assistant works with Project Managers, Project Coordinators and Clinical Research Associates (CRA) at many stages during clinical studies. Works independently to coordinate and manage study deliverables and administrative tasks, as required by the project team. More specifically,