ACUTA
Providing Regulatory Information Management (RIM) solutions and services to the Life Sciences and related industry.
- Open roles
- 40
- New role every
- ~0.1 days
Company signals
Score: 69Job facts
- Location
- Mexico City, Mexico
- Type
- Full-time
- Posted
- Jun 15, 2026
More roles at ACUTA
- Asistente de Datos Junior · Bogota, Colombia
- Analyst (Consulting) · Mexico City, Mexico
- Clinical Research Coordinator, On-site, Elkhorn, NE · Elkhorn, NE, United States of America
- Site Research Assistant (Rosario) · Buenos Aires, Argentina
- Associate Director, HR · Durham, North Carolina, United States of America
- Regulatory and Start Up Specialist - Portugal · Lisbon, Portugal
Site Activation Coordinator
at ACUTA
Job Overview
Under general supervision, perform tasks at a country level associated with
site activation 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 general supervision, perform site activation activities in assigned
studies for investigative sites, according to applicable regulations, SOPs and
work instructions, working closely with the Site Activation Manager (SAM),
Project Management team, and other departments as necessary. Review documents
for completeness, consistency and accuracy, under guidance of senior staff.
• Prepare site regulatory documents, reviewing for completeness and accuracy.
• Inform team members of completion of regulatory and contractual documents
for individual sites.
• Distribute completed documents to sites and internal project team members.
• Support the updating and maintenance of internal systems, databases,
tracking tools, timelines and project plans with accurate and complete project
specific information.
• Review, track and follow up the progress, the approval and execution of
documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator
Pack (IP) release documents.
Qualifications
• Bachelor's Degree Life sciences or a related field (required).
• 1 years of experience in a healthcare environment or clinical research.
Experience as an Intern can be accepted.
• Availability to go to office: Hybrid position.
• Good interpersonal communication and organizational skills.
• Good word processing skills and knowledge of MS Office applications.
• Good attention to detail.
• General awareness clinical trial environment and drug development process.
• Ability to work on multiple projects.
• Ability to establish and maintain effective working relationships with co-
workers, managers and sponsors.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.