Study Start Up Associate Ii

Study Start Up Associate II ( Clinical Site Activation Associate) page is loaded Study Start Up Associate II ( Clinical Site Activation Associate) Apply locations Mexico, Mexico City time type Full time posted on Posted 18 Days Ago job requisition id JR117907 At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner...

Senior Study Start Up Associate page is loaded Senior Study Start Up Associate Apply locations Mexico, Mexico City time type Full time posted on Posted 2 Days Ago job requisition id JR119580 At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and...

At ICON, it's 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 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration,...

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives.ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced...

At ICON, it's 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 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration,...

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives. ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced...

Purpose:The Specialist, Country SSU proactively drives and executes all start up and maintenance related activities and deliverables for assigned studies and sites in their assigned country or countries. Note: Specialists will report into their local country COM but have an operational reporting line to Area and Global SSU Leads_Primary responsibilities:...

ALL CV ́s MUST BE SUBMITTED IN ENGLISH IN ORDER TO BE CONSIDERED Essential Functions:Assist/Advise project teams on all regulatory requirements for clinical studiesPerform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findingsReview and adapt study specific documents according...

United States - New York - New York City United States - Pennsylvania - Collegeville Greece - Thessaloniki United States - Massachusetts - Cambridge We're in relentless pursuit of breakthroughs that change patients' lives. We innovate every day to make the world a healthier place. To fully realize Pfizer's purpose – Breakthroughs that change...

Job Summary:Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Study Start-Up Manager (Regulatory Submissions Manager) to support our growing Study Start-Up/Regulatory Submissions team at Medpace This position plays a key role in the clinical trial management process at Medpace. If you want an...

Associate IICountry: MexicoWHAT YOU WILL BE DOINGMínimo 4 años de experiência en alguna área de expertis de de Santander Corporate & Investment Banking:Global transactional banking, Mercados, Global Debt Financial, ACPM, Corporate Investment Banking, COO. 2.Desempeñar funciones complejas y/o de especialización técnica elevada en alguna de las áreas...

Requisition Number7032Employment Type:RegularWho we areWorldwide, a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company's scientific heritage, our dedicated therapeutic focus on...

i Ad · Clinical Project Manager · Clinical Project Manager · Location : CDMX · Hybrid Work ( 3 office days a week) · Role description · To lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budg ... i Ad Lead Cra i Ad Clinical Project Manager · Clinical Project...

Description Title: Quality Assurance Associate II Job Purpose: The Quality Assurance Associate II (QAA II) is responsible for the oversight and implementation of the Marken Quality Management System (QMS), Marken Standard Operating Procedures (SOPs), processes and policies required to manage and control Marken's Storage, Distribution and Transportation,...

Job Description SummaryLocation: Mexico CityAbout the role:We are seeking a Clinical Research Associate who will supply, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of...

We are looking for a Regulatory & Start Up Specialist to join our FSP team in a Home Based role Job Overview Perform 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...

We are looking for a Regulatory & Start Up Specialist to join our FSP team in a Home Based roleJob 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...

We are looking for a Regulatory & Start Up Specialist to join our FSP team in a Home Based roleJob 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...

Site Management Associate I (SMA I)At ICON, it's 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 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organization:...

Job DescriptionWith support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites.• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.• Performs clinical study site...