Senior Country Start-Up Lead

AbbVie in Mexico City seeks a Sr. Specialist, Country Study Start Up to drive start-up and maintenance activities for assigned studies and sites, ensuring on-time, budget and quality delivery.Acts as site start-up expert and SME, delivering training and change management in new technologies and processes. You will coordinate regulatory submissions, IP...

IQVIA LLC in Mexico is seeking a Sr. Site Contracts Associate with 5 years of CRO/CRO-like experience negotiating clinical site contracts and budget templates. Experience with CRO, pharma, or sponsor environments is required.The role focuses on developing global contracting strategy, supporting start-up contracting activities across sponsors and...

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 made within the timelines agreed with project management and Site...

Job OverviewPrimary 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 the timelines agreed with project management and Site...

Parexel is seeking a Site Activation Partner to lead or support start-up activities for trials in Mexico, Argentina or Brazil. You will manage documents, registrations, and regulatory submissions to enable site activation within timelines.The role requires at least 2 years of start-up experience with US/Canada, and a 7-month temporary assignment with...

Fortrea is seeking a Regulatory Start-up Specialist to act as the local expert for site activation and regulatory submissions. You will collect essential documents, prepare country applications, and liaise with EC/IRB/Regulatory Authorities to meet timelines and sponsor requirements.The role requires 2+ years in clinical research with strong ICH/RA/IRB...

Senior 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 a point of contact for investigative sites and the study team members. This includes supporting site qualification , site level regulatory...

Syneos Health is seeking a Site Activation Specialist II in Mexico City to lead country-level site start-up activities, manage local submissions, and coordinate with CSA/SAM. The role requires strong clinical trial knowledge, vendor management, and excellent communication.You will ensure timely submissions, maintain TMF, and support process improvements in a...

CRA I / CRA II - Site Start-Up & Site Activation | Sponsor-Dedicated | Hybrid (CDMX)Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change...