Job Overview: Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study, to ensure EC/IRB/Third body/Regulatory Authority and any other local applications are
Job Overview: Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within
Site Specialist II - Mexico City only 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,
Site Selection Specialist - Mexico only 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
About Signant Health At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational support — so
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description When you join the team at Thermo Fisher Scientific, you will do meaningful work that makes a positive impact on a global scale. Join 130,000 colleagues who bring our
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.Essential Functions- Under
Company Description Continental is a leading manufacturer and industrial specialist. Founded in 1871, the company generated sales of 19.7 billion euros in 2025 and currently employs around 78,000 people in 54 countries and markets. ContiTech is one
IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years experience negotiating clinical site contracts and budget templates. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience,
At IQVIA Biotech, we partner with visionary biotech companies to transform innovation into patient impact. With dedicated teams, deep therapeutic expertise, and a biotech-tailored delivery model, we accelerate clinical development from early phase through global registrational
Work Schedule Standard (Mon-Fri) Environmental Conditions Office - Collaborates with multiple team members in a matrix environment for the effective delivery of site activation or amendments within assigned projects. - Assists with coordination of the flow
Fortrea is seeking a regulatory affairs professional to support study maintenance and site startup activities, ensuring investigator and regulatory documents meet EC/IRB/Regulatory Authority timelines. With guidance from senior staff, you will develop awareness of applicable regulatory legislation
Fortrea is seeking an experienced regulatory start-up professional to serve as a local expert for site activation and maintenance across countries. You will collect, review, and prepare essential documents for regulatory submissions and ensure timelines align with
Regulatory & Start Up Specialist, cFSP.Location: Mexico - Full home basedJob OverviewThis position will be responsible for participating in end-to-end site management from feasibility to site closure, serving as apoint of contact for investigative sites and the study team members.This
Regulatory & Start Up Specialist, c FSP. Location: Mexico - Full home based Job Overview This position will be responsible for participating in end-to-end site management from feasibility to site closure, serving as a point of contact for investigative
AstraZeneca in Mexico City is seeking a Clinical Study Administrator to assist in coordinating and administering study activities from start-up through close-out, ensuring quality and timely delivery within budget.You will interact with investigators, CRAs and LSAD, maintain the local
IQVIA Argentina is seeking a Senior Regulatory & Start Up Specialist in Ciudad de México. In this role, you will participate in end-to-end site management from feasibility to site closure, acting as a primary point of contact for study sites
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access,
Site Contracts Specialist with experience in Clinical Trials, Home-Based Mexico or Brazil Updated: Today Location: Tlalnepantla, MEX, Mexico Job ID: Description Site Contracts Specialist with experience in Clinical Trials, Home-Based in Mexico or Brazil. Job Responsibilities Administers all
Company Introduction : WorldStrides is the global leader in educational travel and experiential learning. The company was founded in to provide middle school travel programs to Washington, D.C. and has grown to provide a wide range