Research Services Jobs in Mexico City

Job OverviewPerform 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 site monitoring visits (selection initiatio...

Internal Job DescriptionIQVIA Biotech is hiring for Sr. Site Contracts Associate in Mexico with 5 years experience negotiating clinical site contracts and budget templates. Must have CRO Pharma or Sponsor experience.IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With ov...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenance activities.Es...

Job OverviewClinical Trial Educators (CTEs) - Argentina collaborate with research staff and key stakeholders to enhance trial recruitment and support studyspecific training needs. The CTE serves as a strategic partner to internal and external teams optimizing site experience and performance. This ro...

Job OverviewSite Enrollment and Engagement Lead collaborate with research staff and key stakeholders to enhance trial recruitment and support studyspecific training needs. The CTE serves as a strategic partner to internal and external teams optimizing site experience and performance. This role also...

Job OverviewThe Patient Recruitment Specialist is responsible for the operational coordination and delivery of patient recruitment and retention services for assigned clinical studies working in partnership with Patient Recruitment Leads to support successful study execution.The role manages day to...

At IQVIA we are continuously looking for talented individuals who are passionate about advancing healthcare improving patient outcomes and driving innovation through data technology and human ingenuity.By joining our Talent Pool you will be considered for current and future opportunities across vari...

Job OverviewProvides administrative and/or technical support.Essential Functions Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors studies as well as reconcile the total GPS Sponsor balance to the Corporate Sponsor Balance on a monthly basis per SS...

Current University of Arkansas System employees including student employees and graduate assistants need to log in to Workday via then access Find Jobs from the Workday search bar to view and apply for open positions.Students at all University of Arkansas institutions will view open positions and a...

Role OverviewWe are seeking an Associate Principal Primary Intelligence to join IQVIA. This role combines client leadership business development and project delivery with accountability for growing a portfolio of clients and generating revenue.You will lead high-impact primary intelligence engageme...

Job OverviewManage a team of clinical staff supporting clinical studies. Ensure projects are well-resourced and employees are trained and meeting objectives.Essential FunctionsStaff Management: Plan assign and direct work. Assess performance guide professional development reward and discipline emplo...

100% remote roleJob OverviewThe Medical Information Case Processor responsibilities include receiving and documenting incoming telephone calls or emails from investigative sites or other sources reporting Lifecycle Safety Data.This is a trilingual role requiring fluency in English Spanish and French...

Associate Project ManagerRole OverviewThe Associate Project Manager supports the Organizational Effectiveness (OE) team within US Operations working closely with Directorlevel OE Leads on initiatives such as organizational optimization location strategy thirdparty spend and change management.This is...

The Clinical Study Report (CSR) Document Specialists is responsible to populate track QC and perform technical editorial checks of the CSR appendices for assigned studies from authoring until document finalization in the DMS in compliance with current Novartis processes ICH-GCP and relevant regulato...

Internal Job DescriptionJob OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential FunctionsAssist Clinical Research Associates (CRAs) and Regulatory...

Clinical Project Manager Sponsor Dedicated.Clinical Project Managers provides for the regional/global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure regional/global clinical operati...

Job OverviewProject Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet c...

Job OverviewProject Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet c...

Sr. IT Project ManagerJob Overview Enforces organizational policies andestablishesgoals for project teams which develop business applications and information services products.Responsibilities Manages and controls scope schedule and budget formultiple cross functionalprojects.Works with management a...

The Analyst Consulting supports client engagements in the life sciences sector by conducting structured analyses synthesizing insights and contributing to clear datadriven recommendations. Analysts work closely with Consultants Senior Consultants and Engagement Managers to deliver highquality projec...