Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Associate Decentralized Clinical Trial Study Lead (aDCTL) / Decentralized Clinical Trial Lead (DCTL) are an integral part of clinical trial delivery to improve patients’ lives and bring therapies to the market faster. The aDCTL / DCTL roles
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Job Description Join Our Team as a Clinical Research Associate (CRA)! Are you passionate about clinical research and committed to advancing healthcare? We are looking for a Clinical Research Associate (CRA) to support and manage clinical trial sites
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Senior Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more
Job Overview: Responsible for providing coordination and support of projects operated by the Adjudication Services department, to ensure smooth delivery and achievement of the objective that all adjudication events are processed and submitted for adjudication within
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join us as a Manager of Operations – And lead our medical information operations team, oversee the development and dissemination of accurate medical and drug information, ensure compliance with
Senior Pharmacovigilance Associate - Brazil - Remote 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
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Function - R&D Operations Sub function - Clinical Trial Support Category - Analyst, Clinical Trial Support (P4 - E24) Location - São Paulo / Brazil Date posted - Jun Requisition number - R- Work pattern -
The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The aim of this role is to build the relationship with the
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,
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Summarized Purpose : Essential Functions : - Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more
Senior Project Manager São Paulo – São Paulo – Brazil – Hybrid (Twice a week at Cidade Jardim) Who We Are Intrials is a disruptive company with all the attributes that a CRO must master. We
Vibra Travels is seeking a travel nurse RN Long Term Acute Care for a travel nursing job in Clairemont, California. Job Description & Requirements Specialty: Long Term Acute Care Discipline: RN Duration: 13 weeks 36 hours per
ARMStaffing is seeking a travel nurse RN Long Term Acute Care for a travel nursing job in Bethlehem, Pennsylvania. Job Description & Requirements Specialty: Long Term Acute Care Discipline: RN Start Date: 04/21/2025 Duration: 13 weeks 36
ALL CV´s MUST BE SUBMITTED IN ENGLISH IN ORDER TO BE CONSIDERED! Essential Functions : - Assist/Advise project teams on all regulatory requirements for clinical studies - Perform compliance assessments according to country requirements and document
Sr. CRA 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
Job Overview : Summary of Responsibilities : - To serve as contact for project team and investigative sites, conduct site contacts and document contacts for assigned sites as required per study guidelines, including creating contact reports