Join a Team That’s Advancing Clinical Research We’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional teams to ensure studi
🚀 Lead Global Clinical Trials That Change Lives IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. CTM II
Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions• Perform site monitoring visits (selection, init
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring visits (selection, in
IQVIA Clinical Functional Services Partnerships (FSP) business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our customers. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical stud
Join a Team That’s Advancing Clinical Research We’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional teams to ensure studi
Clinical Research Coordinator - El Paso, TX Work Set-Up: On-siteSchedule Weekly Hours: 24 hours/week About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmace
Exceptional care starts with exceptional people. For us, this is more than a job– it’s a calling. It’s waking up each day, looking for ways to make a difference with a compassionate, inclusive and talented team. Ochsner empowers you to discover your passion, reach your potential, and Pursue Your Pur
A Senior Clinical Research Coordinator position is available within the Tisch Cancer Institute. The Senior Clinical Research Coordinator will work with Principle Investigators (Pis), Research Manager and Clinical Research Team to manage data associated with cancer clinical research protocols. Under
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates. Why IQVIA? Career development opportunities to grow as we grow Flexible working to assist work–life balance and professi
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions• Perform site monitoring visits (selection, ini
背景要求: 1. 满足以下任意要求: 1年以上CRC/CTA/SSU工作经验; 5个月以上CRA经验; 2. 本科及以上学历 3. 英语听说读写流利 职位优势: 系统化培训:4周全脱产培训,快速提升专业能力 薪酬福利:具有市场竞争力的薪资,完善的福利体系 完善保障:五险一金 + 补充商业医疗保险 休假权益:充足的带薪年假与病假,工作生活更平衡 成长空间:清晰的职业发展路径,助你稳步晋升 强大支持:全球领先药企与IQVIA的培训体系,资源与平台双重加持 IQVIA is a leading global provider of clinical research services, commer
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring visits (selection, in
Under minimal supervision, coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists in protocol submissions (for e.g., Institutional Review Board, Grants and Contr
We are hiring CRAs and SCRAs in Central & Western Ukraine! Join IQVIA and take the next step in your clinical research career. Be part of a global team and make a meaningful impact on patients’ outcomes Your responsibilities will include: Performing site selection, initiation, monitoring and close-o
The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research Coordinator, but due to abbreviated hours doesn't qualify for exemption. This is an hourly position which is eligible for overtime only intended to be used for part-time employees. The Clinical Resear
Job Overview Clinical Research Associate performs monitoring and site management work to ensure that sites are conducting the studies and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions: Perform site monitor
Under general supervision, generates, reconciles and interprets highly complex clinical research data; conducts clinical testing and develops protocols. Develops workflow policies and procedures. Mentors, trains and reviews the work of less experienced clinical research staff. Oversees the clinical
The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office). Co
The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research Coordinator, but due to abbreviated hours doesn't qualify for exemption. This is an hourly position which is eligible for overtime only intended to be used for part-time employees. The Clinical Resear
Get weekly curated job picks, salary trends, and career insights delivered to your inbox.
Subscribe and get 10% off your first payment.