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- ...As part of our global team, you’ll have the opportunity to perform remote activities on assigned projects in liaison with the CRA and study Clinical Lead. As an Assistant Clinical Research Associate, you'll provide support with site preparedness, logistical support...Trabajo remoto
- Senior Clinical Research Associate responsible for site monitoring, site management, and regulatory compliance across clinical studies. Leads projects of limited scope and manages study sites according to sponsor procedures and regulatory guidelines. Responsibilities...
- ...CRA - All veleves | Vaccine At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative...Trabajo remoto
- Thermo Fisher Scientific seeks a Clinical Research Associate (Level II) to monitor investigational sites and manage clinical trial compliance remotely or on-site in Argentina. The role involves conducting site visits, ensuring protocol adherence, managing documentation...
- ...The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials. This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data, compliance with regulatory...
- JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical...Trabajo remoto
- Thermo Fisher Scientific seeks a Clinical Research Associate to monitor and manage clinical trial sites, ensuring compliance with protocols, ICH-GCP guidelines, and regulatory standards. The role involves coordinating with investigative sites and cross-functional teams...
- ...CRA II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how...Trabajo remoto
- Thermo Fisher Scientific seeks a Senior Clinical Research Associate to monitor investigational sites, ensure protocol compliance, and manage clinical trial documentation. The role involves remote and on-site visits across multiple studies, coordinating with sponsors and...
- ...IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in any of the following therapeutics: oncology, cardiovascular or internal medicine: IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years...
- ...that help bring breakthrough treatments to patients faster. We are seeking an experienced Senior Clinical Research Associate (Sr CRA 3) to join our Clinical Monitoring team in Argentina. In this role, you will independently manage and monitor clinical trial sites to...
- ...or Registered Nursing certification Minimum 3 years of completed on-site clinical monitoring experience Minimum 2 years as lead CRA on Oncology and/or Hematology trials Strong knowledge of ICH-GCP guidelines and applicable regulations Risk-based monitoring...
- Thermo Fisher Scientific seeks an experienced Senior Clinical Research Associate to conduct remote and on-site monitoring of clinical trial sites across rare diseases and Alzheimer's studies. The role involves ensuring protocol compliance, managing documentation, and coordinating...
- ...Sr. CRA I Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity,...
- Buenos Aires, Argentina Full time R1562678 Job Overview Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical...
- Worldwide Clinical Trials is hiring a Clinical Research Associate II - Hematology for Argentina. This home-based role supports sites across Argentina with regional travel 6–10 days per month, coordinating site visits and study activities to ensure quality and regulatory...
- ...Why Syneos Health CRA II Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities...
- ...Clinical Research Associate to join our Monitoring Resource team. This remote freelance role is based in Argentina and reports to the CRA Line Manager. You will perform site visits, verify source data, ensure regulatory compliance with FDA/ICH-GCP, and support data...
- Worldwide Clinical Trials Holdings, Inc. seeks a Clinical Research Associate to monitor sites across Argentina from a home-based role. You will perform site qualification, initiation, monitoring, and close-out visits, ensuring compliance with GCP, study protocols, and ...
- Thermo Fisher Scientific seeks a Clinical Research Associate I to monitor investigational sites and manage clinical trial compliance. The role involves conducting remote and on-site visits, ensuring protocol adherence, documenting findings, and coordinating between sites...
- ...with GCP and ICH, ensuring patient safety and data quality while collaborating with study teams. Ideal candidates hold an MD or Pharmacy degree with CRA experience, possess strong communication and organizational skills, and are fluent in English and #J-18808-Ljbffr...
- ...Sr CRA - Sponsor dedicated - Argentina Home Based Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address...
- ...information as necessary to determine overall readiness of the patient information for next level review. Interaction with sites/CRA and follow-up on study required milestones from the project start until close out. May act as backup/ perform the activities as per...
- ...CRA 2 - Homebased This role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance...
- ...and or audits of the Trial Master File (TMF) to ensure inspection readiness. May support clinical monitoring activities, such as CRA training, visit report review, site letters, and escalated site issues May track site qualification, initiation, routine and close...
- ...are aligned to the critical path for site activation. • Achieves PPD’s target cycle times for site. • May work with the start-up CRA(s) to prepare the regulatory compliance review packages, as applicable. • May develop country specific Patient Information Sheet/Informed...Trabajo remoto
- ...ensures regulatory compliance with ICH-GCP standards, performs monitoring activities, and develops new research sites while reporting to a CRA manager. Responsibilities Build and maintain strong site relationships throughout all trial phases Perform remote and on-...
- ...not limited to ISO, NIST, COBIT, PCI DSS, and the Unified Compliance Framework, as well as regulatory requirements such as GDPR, DORA, CRA, and SOX. ~ Experience applying risk and control concepts to evaluate control effectiveness, support methodology development, and...
- ...study projects Strong experience leading and managing local, regional, and international vendors Previous experience as a Senior CRA Advanced English proficiency What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve...Trabajo remoto
- ...Qualifications Bachelor's Degree in health related disciplines (Medical, Scientific, Nursing) preferred. Previous experience as CRA is required (performing investigation monitoring and similar functions). Minimum of 1 year of clinically related experience, of...
