Study Start Up Associate I 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
Description The Strategist, Patient Recruitment & Site engagement works with the Associate Director, Patient recruitment strategies and Development and the Specialist, Multimedia & Recruitment in supporting patient recruitment strategies and site engagement. This role will be perfect
Company Description Milestone One is a Site Enabling Organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need, and our mission is to strengthen study delivery by connecting sponsors, CROs, and medical institutions through
Job Overview: Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Research Associate (CRA / Sr. CRA) At Thermo Fisher Scientific, our Clinical Research team supports leading pharmaceutical, biotechnology, and emerging biopharma companies in advancing
Clinical Research Associate II (FSP - Sponsor Dedicated) 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,
SSU CRA 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, anticipate
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials according
Proposal Analyst 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, anticipate
Why This Role Matters Are you ready to take your monitoring expertise to the next level and mentor the next generation of clinical research professionals? As a Senior Clinical Research Associate I (SCRA I), you will
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. We are
Patient Concierge Coordinator 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,
Company Description Medicine moves forward here. So will you. Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. We focus on the most complex trials, the studies where experience, judgement,
The Strategist, Patient Recruitment & Site engagement works with the Associate Director, Patient recruitment strategies and Development and the Specialist, Multimedia & Recruitment in supporting patient recruitment strategies and site engagement. This role will be perfect for
Study Start Up Associate I 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
Job Description Please submit CV in English. The Milestone One Senior Clinical Site Coordinator is a key member of the Operations team, taking hands-on responsibility for the preparation, activation, and day-to-day coordination of clinical trial activities at
When our values align, theres no limit to what we can achieve. Parexel FSP is hiring a Site Activation Partner in Mexico, Argentina or Brazil ! Candidates must have at least 3 years of experience in
When our values align, theres no limit to what we can achieve. Parexel is looking for multiple Site Monitors II (CRA II) in Argentina, Brazil and Mexico. The Site Monitor II will be responsible for data
IQVIA Biotech is hiring for Sr. Site Contracts Associate in with 3-5 years experience negotiating clinical site contracts and budget templates. Grant Plan a plus. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over
When our values align, theres no limit to what we can achieve. Parexel FSP is hiring multipleSite Care Partners inArgentina (Buenos Aires)! Excellent opportunity for experienced Senior CRAs with +5 years of experience, ready to