Clinical Research Associate I

**About the role**: Curebase is seeking a Clinical Quality Associate I who will thrive in a quickly scaling healthcare technology environment. Quality at Curebase is deeply cross-functional, and you will work with nearly every function at the company to conduct risk-based quality management (RBQM) surveillance of Clinical Operations activities at Curebase....

PLEASE SUBMIT ALL RESUMES/CV'S IN ENGLISH FOR CONSIDERATION PREFERRED EXPERIENCE: Pharmaceutical/Biotech Industry, Hematology, Oncology Company Overview: BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160) is a global, commercial-stage, research-based biotechnology company focused on molecularly targeted and immuno-oncology cancer therapeutics. With a team of over...

**Company Description** We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to...

**Principal Clinical Research Associate** **Please submit your CV in English for Quickest Review Process!** Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can provide an update on a study or...

Company OverviewFortrea is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.We...

**Company Description** Describe the primary goals, objectives or functions or outputs of this position. To enable AbbVie’ s emergence as a world class R&D organization, the position anticipates and proactively solves studyrelated clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol...

About the RoleWe are seeking an experienced Clinical Research Associate II to conduct onsite monitoring visits in Brazil. This role offers the opportunity to build and maintain site relationships, ensuring they're set up for success.Key ResponsibilitiesLeverage your expertise to conduct qualification visits, site initiation visits, monitoring visits, and...

AstraZeneca is one of the most fascinating biopharmaceutical companies in the world. From researchers to sales people, from lab technicians to the legal department, we all have a mission to turn ideas into science, science into revolutionary medicines that save and extend patients’ lives and benefit society. Our portfolio is solid and our pipeline is...

**Senior Clinical Research Associate** **(Level dependent on experience)** Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can provide an update on a study or milestone that they have achieved....

Job SummaryWe are seeking a highly skilled Clinical Research Associate (CRA) Manager to join our team at Iqvia Argentina. As a CRA Manager, you will be responsible for overseeing the execution of clinical trials, ensuring compliance with regulatory requirements, and providing guidance to junior CRAs.Key ResponsibilitiesMonitor and manage clinical trial sites...

**Clinical Project Manager** **(Level Depends on Experience)** **Job Purpose/Summary**: Responsible for management and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client’s goals of time, budget and quality performance are met. The Clinical Project Manager I is expected to require support and guidance from Directors and/or...

About the RoleWe are seeking a highly skilled Clinical Research Associate to join our team as a Study Monitor. As a key member of our Centralized Monitoring School, you will be responsible for providing project-related assistance to assigned project teams, ensuring all work is conducted in accordance with standard operating procedures, policies, good...

Job Title: Senior Clinical Research SpecialistAbout the Company:ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Clinical...

About ICON PlcICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We advance clinical research by providing outsourced services to pharmaceutical,...

The Ass CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight and impact on local regulatory and financial compliance, at a country operations level at the client in compliance with ICH GCP and country regulations. The position has a significant impact on how a country can deliver...

**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 compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event...

In Parexel we are looking for experienced CRA to make onsite monitoring visits in Brazil. Oncology experience is required. Your time here At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRAs are accountable for using their expertise to build and maintain the site relationship and ensure they’re set up...

In Parexel we are looking for experienced CRA to make onsite monitoring visits in Brazil. Oncology experience is required. Your time here At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they’re set...

Our clinical trial activities in South America are increasing rapidly! We are currently seeking a full-time, office-based Clinical Research Project Coordinator to join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where...

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...