Manager, Regulatory & Start Up – Sponsor Dedicated Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Data Team Lead – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than
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
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Clinical Vendor Oversight Specialist Make an impact. Advance science. Grow your career. At Thermo Fisher Scientific, youll be part of a global team committed to making the world healthier,
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than
Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all
Job Summary The Study Manager is part of the ( DMTI - Digital Medicine and Translational Imaging ) group, that looks to develop and implement novel technologies to support companys portfolio studies. In particular for this
Job Summary The Clinical Scientist (CS) will provide of observational study execution including epidemiological, non-interventional, pragmatic and low-interventional studies and research collaborations to ensure consistency of approach, conduct, monitoring, analysis, reporting, and oversight of core team
Home Based - México ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion
Job Summary The RCA Specialist will be accountable to train Sr / Issue Leads on the investigation/root cause analysis, corrective/preventive action (CAPA) plan development and effectiveness checks for assigned Quality Events (QEs). This individual will also
Location: Mexico Employment Type: Full-Time Open Positions: 2 Key Responsibilities (but not limited to)- Use & ensure that Standard Operating Procedures (SOPs) concepts, practices in a time sensitive manner for all delegated projects and tasks. Responsible
Job Summary The Patient Compensation Lead will be responsible for ensuring all processes and vendors are in place that are needed to enable participant compensation, reimbursement, and travel services.This role will be accountable for the performance
Job Summary - Accountable for all country clinical/medical aspects associated with Development and prioritized Re - search programs/trials by providing clinical strategic and tactical leadership as the Country Clinical Development representative. May work across several countries.
Parexel FSP is hiring multiple Site Activation Partner in Mexico! The Site Activation Partner (SAP) is responsible for leading or supporting operational activities from start - up to close-out, for assigned studies and investigator sites to ensure
Parexel FSP is hiring multiple Country Study Operations Managers (cSOMs) in Brazil, Chile and Mexico . The Country Study Operations Managers (cSOM) will have responsibilities for study and regional or specific country level activities from study startup
Position Overview The MLR Facilitator is responsible supporting MLR (Medical, Legal & Regulatory) content approval process, for system governance, quality assurance, and cross-collaboration support for the FUSE Digital Asset Management (DAM) system. This role serves as