Support pharmaceutical and biotechnology clinical trials in Argentina through site activation, regulatory documentation, feasibility activities, eTMF management, and investigator-site coordination.
Support clinical trial site activation, regulatory documentation, feasibility work, and site communications for a global clinical research organization. Maintain trial systems, study files, metrics, and investigator site materials.
United States
MassachusettsSupport Obsidian Therapeutics’ engineered cell and gene therapy trials by coordinating clinical sites, patient scheduling, vendors, and biospecimen logistics.
Support global clinical research projects by coordinating trial documentation, regulatory materials, study systems, metrics, and site operations. The role also contributes to project administration, team coordination, training, and process improvement.
Coordinate clinical trial operations in support of pharmaceutical and biotechnology studies at a global research services organization. Manage trial documentation, regulatory materials, study systems, performance metrics, and site supplies.
Coordinate sponsor-site activities, regulatory documentation, clinical supplies, and study tracking for Syneos Health’s biopharmaceutical trials. Support site communications, meetings, audits, and corrective actions across assigned studies.
United States
North CarolinaRemoteFull-timeMiddleSeniorEnglish RequiredClinical Trial CoordinatorGeneralSupport pharmaceutical and biotechnology clinical trials as a Clinical Trial Coordinator. Manage site activation, regulatory documentation, feasibility activities, trial systems, and investigator-site communication.
United StatesNorth CarolinaRemoteFull-timeJuniorMiddleNo degree requiredEnglish RequiredClinical Trial CoordinatorGeneralSupport global pharmaceutical and biotechnology studies through site activation, regulatory documentation, feasibility activities, trial-file maintenance, metrics tracking, and investigator communications.
Support pharmaceutical and biotechnology clinical trials remotely from Colombia. Coordinate site activation, regulatory documentation, feasibility activities, file reviews, and clinical trial systems.
Coordinate clinical trial start-up, feasibility, regulatory submissions, documentation, and site communications for a global clinical research organization. Maintain clinical systems, investigator files, study metrics, and related trial records.
Support clinical trial site activation, feasibility, regulatory submissions, documentation, and study systems from a remote role based in Mexico. Provide administrative and technical coordination for pharmaceutical and biotechnology research programs.
Coordinate site activation, feasibility, regulatory documentation, trial systems, and study support activities for clinical research projects in Mexico. Support pharmaceutical and biotechnology clients through global clinical research services.
Support pharmaceutical and biotechnology clinical trials through site activation, electronic trial master file documentation, regulatory submissions, and feasibility activities. This is a fully remote position based in the Philippines.
