Company DescriptionJob DescriptionPurpose Statement:Collaborate with the coordination of planning, implementation, and conduction of local and general clinical studies (Post-Marketing Observational, Multi-Country Non-Interventional, Investigator Initiated, Non-AbbVie Sponsored Collaborative and Pharmacoeconomic) and Pre-Approval Access programs (PAAs) according to Abbvie
Link-Worldwide is hiring for a position focused on the planning and execution of clinical studies across Mexico. The role involves managing regulatory documents, collaborating on publications, and ensuring compliance with Good Clinical Practices.Applicants should have a medical, pharmacy, or
Job OverviewThe Product Analyst will assist in the development of software products, IT solutions and define the vision, strategy, and priorities at Fortrea. The Product Analyst gathers and prioritizes requirements, communicates with stakeholders, and makes decisions
Worldwide Clinical Trials is looking for a Team Lead for TMF Operations in Mexico, Ciudad de México.This pivotal role involves maintaining compliance with Trial Master Files and driving the objectives of Project Teams across various studies.As Team
Job SummaryPerforms assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials.Responsible for delivery with oversight from Line Manager in areas such as investigator site contracts, ethics and regulatory
Project Manager – Global Delivery (Advisory / eCOA / RTSM)At Signant Health, we are on a mission to help bring life‐changing treatments to patients faster.As a general leader in clinical trial technology and services, we operate at
Fortrea is a leading integral contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience.We provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology
Are you driven by intellectual curiosity and a desire to solve meaningful problems? Do you thrive on building client relationships, innovating solutions, and interpreting data to drive impactful outcomes? If so, join our Health Solutions team!
Job Overview The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTA shall reflect their experience, and level
CDMXWhat You Will DoTrial Documentation & eTMF ManagementOversee clinical trial documentation, including CTA packages for Health Authority (HA) and Ethics Committee (EC) submissions.Maintain and ensure compliance of the electronic Trial Master File (eTMF), including timely uploads, quality
Pharmacovigilance Assistant IIICON plc is a leading healthcare intelligence and clinical research organization that supports pharmaceutical, biotechnology, medical device, and public health organizations.ResponsibilitiesDistribute incoming safety notifications.Submit, file and track safety‐related information.Prepare, organize and maintain files, reports, listings
At ICON, its our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients lives. Our
Pharmacovigilance Assistant II ICON plc is a leading healthcare intelligence and clinical research organization that supports pharmaceutical, biotechnology, medical device, and public health organizations. Responsibilities Distribute incoming safety notifications. Submit, file and track safety‐related information. Prepare, organize
Job FunctionR OperationsJob Sub-FunctionClinical Trial Project ManagementJob CategoryProfessionalAll Job Posting LocationsMexico City, MexicoAbout Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.Visionaries like you work on teams