Are you ready to transform clinical trial start-up timelines in one of the most complex regulatory environments? We are looking for a strategic and hands-on leader who can challenge the status quo, optimize processes, and drive faster,
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
Team Introduction The TikTok LIVE teams mission is to work hand-in-hand with LIVE creators, agencies, and partnership organizations to create an environment that brings communities together in real time to create meaningful and interactive connections around
H.B. Fuller is seeking a dedicated individual to lead daily production activities in Monterrey, Nuevo León. You will coordinate production tasks and ensure adherence to company protocols while working in a collaborative environment. The ideal candidate
H.B. Fuller is looking for a Process Engineer in Piedras Negras, Coahuila, to support the construction and operation of a new manufacturing facility. The role involves optimizing production processes, managing capital projects, and ensuring compliance with
Home Based - CDMX 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 inclusion
Job Summary: Join Medpace at our Mexico City offfice! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start up! You will
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Solid organizational and negotiation skills - Strong attention to detail - Proven ability to handle multiple time sensitive tasks efficiently and effectively - Flexible and able to reprioritize workload
Summarized Purpose : Completes site activation or amendment deliverables within the assigned projects and ensures all project deliverables meet customer expectations, as well as, contracted deliverables by providing accurate projections, report updates, and ongoing risk assessments.
A leading clinical research organization in Mexico City is seeking an experienced Regulatory Submissions Manager for a full-time, office-based role. This position is crucial for the study start-up process, requiring a bachelors degree in life sciences and
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
MMR Consulting is seeking a Sr. C&Q Engineer in Tijuana, Mexico, to lead teams in the validation of biopharmaceutical systems and equipment. With a focus on commissioning and qualification, the role includes technical guidance, project management,
Syneos Health in Mexico City is seeking a Site Activation Specialist I to manage the start-up of investigative sites for clinical trials. This role includes ensuring compliance with timelines, budgets, and quality standards, as well as liaising
Contemporary Star Energy, a joint venture located in Zaragoza, is seeking a Maintenance Manager to lead the maintenance strategies for production equipment. Aumente sus posibilidades de conseguir una entrevista leyendo la siguiente descripción general de este
Position Summary The Clinical Start-Up & Trial Lead (Start-Up + CTL) is responsible for the strategic planning, coordination, and oversight of clinical trial start-up activities as well as the ongoing execution of clinical studies. This hybrid role ensures operational
A leading adhesives manufacturer in Piedras Negras seeks a Process Engineer to support the construction and operation of a new manufacturing facility. This role involves developing and optimizing processes to meet safety, quality, and efficiency goals
We’re expanding our capabilities across Mexico, Brazil, Argentina, Colombia, Chile, and Peru, and we’re hiring a Senior Regulatory and Start Up Specialist (Senior RSS) in Mexico! As the Senior RSS on our team, you are a seasoned, experienced
A clinical research organization in Mexico City is seeking a Regulatory Submissions Coordinator to support Regulatory Submissions and gain vital experience in study start-up. Responsibilities include providing support activities, ensuring compliance, and conducting document quality control. Requirements
As a member of the executive leadership team, the Plant Manager is responsible for the cost effective operations and for the infrastructure to deliver high quality products and services. Establishes goals, monitors work/workflow, and evaluates results
Syneos Health, Inc. is seeking a Site Activation Specialist in Tlalnepantla, Mexico. This role involves overseeing the start-up of investigative sites for clinical trials, ensuring compliance with timelines and monitoring financial aspects of projects. The ideal candidate