Research Protocols Trabajos En México - 156 Job Positions Available

Job Description Summary: Monitors patient data and study-related information related to clinical study sites and clinical trial participation.
Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into data validation plan.Job Description: 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.The Research Project Manager is responsible for overseeing the entire lifecycle of a research project, from initial concept development to data analysis and reporting.
Ensures that the projects stay on track with timelines, budget, and objectives.
Manages research coordinators.Knowledge and Skills Required:Knowledge in Project Management and site management.Strong organizational skills with demonstrated success required.Ability to make decisions independently and oversee important activities relevant to clinical research activities according to predetermined global standards.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 you.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 monitoring and site management work.#J-18808-Ljbffr