Clinical Research Associate Iii

Principal Clinical Research AssociatePlease 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 milestone that...

Principal Clinical Research AssociateJob SummaryCTI Clinical Trial Services, Inc. is seeking a highly skilled and experienced Principal Clinical Research Associate to join our team. As a key member of our clinical operations team, you will be responsible for overseeing the management of clinical trials, ensuring compliance with regulatory requirements, and...

**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 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...

Job SummaryThermo Fisher Scientific is seeking a skilled Clinical Research Associate to join our team. The successful candidate will be responsible for monitoring investigator sites with a risk-based approach, ensuring data accuracy, and conducting site initiation and close-out activities. This role is ideal for a detail-oriented professional with experience...

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...

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...

Descrição da vagaTo enable AbbVie’ s emergence as a world class R&D organization, the position anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol level execution of SMM deliverables involving start-up, execution, and close-out of...

At Milestone One, we're on a mission to support clinical study sites in delivering stronger studies. To achieve this goal, we're seeking an experienced Senior Clinical Research Associate to join our team.About the RoleWe're looking for a highly skilled SCRA professional to find and build relationships with new clinical trial sites, actively promoting our...

PLEASE SUBMIT ALL RESUMES/CV'S IN ENGLISH FOR CONSIDERATION Language Requirement: Fluent English and Portuguese. Spanish is a plus. 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...

At Lilly, we are committed to making life better for people around the world. Our team of professionals works to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. To achieve this mission, we need a skilled Clinical...

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...

Job SummaryWe are seeking a Senior Clinical Research Associate to join our team at BeiGene. In this role, you will be responsible for conducting site visits, monitoring data quality and patient safety, and ensuring compliance with ICH-GCP guidelines.About the RoleThe Senior CRA will assume the role of a primary CRA, conducting site visits, managing...

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...

Job Title: Clinical Research Associate II Job Overview: The Clinical Research Associate II monitors investigational sites to ensure subject safety and provides high-quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/ International Conference on Harmonization (ICH)...

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...

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...