Clinical Trial Site Activation Specialist

Worldwide Clinical Trials in Mexico City seeks a Senior Clinical Research Associate to lead site management activities across a regional footprint. You will coordinate clinical staff, ensure site qualification, initiation, monitoring, and close-out in line with protocol and SOPs.You will monitor data quality, TMF compliance, and risk management, while...

IQVIA LLC in Mexico City is seeking a Site Activation Coordinator to perform country-level activation tasks for investigative sites under supervision. You will prepare regulatory documents, track progress, and coordinate with the Site Activation Manager and cross-functional teams to ensure timely document completion.The role requires a life sciences degree...

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...

IQVIA in Mexico City is seeking a Site Activation Coordinator to support country-level regulatory and activation tasks for clinical studies, working with the SAM and PM teams to ensure documents are complete and accurate.You will review regulatory and contractual documents, prepare site packs, distribute materials to sites, and maintain project trackers and...

Worldwide Clinical Trials seeks a regulatory start-up professional to manage end‑to‑end site activation for awarded projects. You will coordinate regulatory submissions, essential document collection, and country‑specific requirements to support timely site initiation.Responsibilities include local liaison for regulatory activities, customization of...

IQVIA is seeking a Regulatory Site Activation professional in Mexico City to perform regulatory and site activation tasks within local and international guidelines. You will review documents, prepare regulatory materials, and coordinate with the Project Management team and SAM to ensure compliant site activation across studies.The role requires office...

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...

A biopharmaceutical solutions organization in Mexico is seeking a Clinical Trial Manager to oversee site activities, ensuring compliance with Good Clinical Practice and protocol adherence. Responsibilities include conducting site qualifications and monitoring, managing site staff, and documenting all project activities. The ideal candidate holds a Bachelor's...

A leading biopharmaceutical solutions organization based in Mexico City is seeking a professional to oversee site activations for clinical trials. Responsibilities include managing regulatory submissions, ensuring compliance with timelines, monitoring project budgets, and liaising with investigators. The ideal candidate will have a degree in Life Sciences,...