Digital Support Coordinator (Overnight)
Avery DennisonProvide overnight Tier 1 technical support for Avery Dennison’s labeling and digital identification solutions. Triage tickets, resolve client issues, and escalate complex cases.
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Worldwide Clinical Trials is a global contract research organization that supports pharmaceutical and biotechnology companies throughout the drug development lifecycle. With more than 30 years of experience, the company provides clinical monitoring, data management, patient recruitment, and regulatory consulting across therapeutic areas including oncology, cardiology, and rare diseases. Its approach combines broad clinical trial expertise with personalized support and tailored solutions for complex studies.
Remote Clinical Trials Associate in Argentina
Support documentation, system access, training, and project tracking for Worldwide Clinical Trials’ global research projects. Remote role serving Argentina, Mexico, and Brazil.
Description
- Help clinical project teams with administrative tasks and project tracking
- Manage system access requests for Project Managers, Lead CRAs, and CRAs, and monitor their progress
- Keep project portals up to date and check document versions for accuracy
- Assist with preparing, shipping, version-controlling, and filing trial records, including Investigator Site Files and Trial Master File documents
- Maintain project records, such as site medical question-and-answer logs and details about participating sites and staff
- Prepare and share minutes from sponsor, project, and internal management meetings
- Organize and monitor training specific to each project
- Carry out administrative tasks accurately and on time to support effective clinical trial delivery
- Work across time zones with Project Managers, Lead CRAs, CRAs, and colleagues around the world
Requirements
- A degree or equivalent experience
- At least one year of experience in a related role
- Strong written and spoken English
- Fluency in the language of the country where the role is based
- Knowledge of ICH, GCP, and applicable FDA or EU directive regulations
- Strong organizational, problem-solving, and interpersonal abilities
- Excellent attention to detail and quality
- Ability to work independently and collaboratively
- Ability to manage competing priorities, use independent judgment, and adapt in a fast-changing environment
- Excellent command of Microsoft Office, including Outlook, Word, Excel, and PowerPoint
Benefits
- A collaborative, inclusive workplace
- Opportunities for career growth and development
- Opportunities to learn and grow
- Meaningful work that helps improve patients’ lives through clinical research
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