Clinical Process Coordinator
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Before you apply
LocationMexico City, Mexico
SeniorityEntry
ExperienceUp to 1 yrs
Company size10,000+ people
PostedOct 27, 2026 · 1w ago
Verified live2d ago
At a glanceSummarised by Seekless from the posting.
Knowledge of GCP and clinical research processes
Strong organizational skills and attention to detail
Ability to manage multiple tasks and priorities while meeting established timelines
Good written and verbal communication skills
Ability to work effectively within a cross-functional and multicultural environment
Good working knowledge of Microsoft Office, particularly Excel, PowerPoint, Outlook, Teams, and SharePoint
Ability to work with trackers, reports, documentation, and clinical systems
Strong focus on quality, compliance, and accurate documentation
English proficiency sufficient to communicate effectively in a global business environment
Bachelor’s degree completed preferably in Life Sciences, Healthcare, Pharmacy, Biology, Administration, or a related field
6 months - 1 Year of previous experience in Clinical Research, Clinical Operations, or the pharmaceutical industry is preferred. An Internship experience works.
Skills
Microsoft Excel
Microsoft PowerPoint
Microsoft Outlook
Microsoft Teams
Microsoft SharePoint
CTMS
TMF/eTMF
Job Overview
Provide project related assistance for all assigned project(s), sites and project teams. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.
Responsibilities
Essential Functions• Support Clinical Operations activities under the supervision of the Study Process Lead.
• Manage TMF/eTMF activities, including filing, reconciliation, QC, and document review.
• Upload and reconcile regulatory documentation in designated systems.
• Track study, site, subject, visit status, and key milestones in CTMS.
• Support study payment processes and financial/invoice reconciliations.
• Generate and maintain operational reports, trackers, and dashboards.
• Support Feasibility activities, including site identification, FQ creation, follow-up, and reporting.
• Perform key study reconciliations and reporting, including IMP reconciliation and PD Listings.
• Support study close-out activities and documentation completeness assessments.
• Provide day-to-day operational and administrative support, including document management, SharePoint organization, system access, and study-specific activities.
Qualifications
• Bachelor’s degree completed preferably in Life Sciences, Healthcare, Pharmacy, Biology, Administration, or a related field.
• 6 months - 1 Year of previous experience in Clinical Research, Clinical Operations, or the pharmaceutical industry is preferred. An Internship experience works.
• Knowledge of GCP and clinical research processes.
• Strong organizational skills and attention to detail.
• Ability to manage multiple tasks and priorities while meeting established timelines.
• Good written and verbal communication skills.
• Ability to work effectively within a cross-functional and multicultural environment.
• Good working knowledge of Microsoft Office, particularly Excel, PowerPoint, Outlook, Teams, and SharePoint.
• Ability to work with trackers, reports, documentation, and clinical systems.
• Strong focus on quality, compliance, and accurate documentation.
• English proficiency sufficient to communicate effectively in a global business environment.
About the company
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
Legal
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.