.Job Description: Knowledge in Project Management and site management.
- Strong organizational skills with demonstrated success required.
- Requires ability to make decisions independently and oversee important activities relevant to clinical research activities according to predetermined global policies.Company Description: PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time.Job Overview: 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.Are you passionate about clinical research and ensuring the safety and well-being of patients? Do you have experience as a Clinical Trials Assistant and want to take the next step in your career? We are looking for a Clinical Research Associate.Clinical Research Associate Location: CDMX, MTY or GDL Availability to travel to the US Hybrid work. The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the process.Job Overview: Provide comprehensive data management expertise to the Data Management (DM) team, ensuring efficient and high-quality data management products that meet sponsor and company needs. Perform Clinical Data Management and/or Coding activities, and may provide leadership.Job Overview: Manage the end-to-end delivery of data management services for single or multi-service projects with minimal guidance, ensuring quality deliverables are provided on time and within budget to meet customer satisfaction.Job Overview: Provide both basic and comprehensive data management expertise to the Clinical Data Management (CDM) team, ensuring the delivery of efficient, high-quality data management products that meet customer needs. You may also take on team leadership responsibilities.Job Overview: Perform daily administrative activities in collaboration with Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams to ensure the accurate delivery of the Trial Master File (TMF).Essential Functions: Assist CRAs and RSU teams with necessary tasks to ensure compliance and efficient study execution.Assoc. Clinical Operations Lead: The Assoc. COL leads the execution of the Site & Patient Services (SPS) components of Real World Late Phase Research (RLWPR) studies by applying clinical research expertise, exceptional decision-making skills, and innovative approaches to problem solving.Clinical Data Programmer: 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 the future