Global Clinical Start-Up Specialist

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...

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...

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...

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...

Syneos Health, Inc. is seeking a CRA I/II for Site Start-Up and Activation in a hybrid role based in CDMX. You will perform site qualification, initiation, monitoring, and close-out activities, ensuring regulatory compliance and data integrity while collaborating with the project team.The role requires strong communication skills, proficiency with data...

Home Based - MexicoAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit...

Syneos Health is seeking a Site Activation Specialist to lead country-level start-up activities within regulatory, EC and RA submissions, ensuring timely Site Start-Up processes across trials.You will coordinate with CSA/SAM, manage essential document packages, liaise with Investigational Sites and local authorities, and monitor submission timelines while...

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 the timelines agreed with project management and Site...