Overview
Supports clinical trial project teams with trial coordination, site activation, feasibility, documentation, systems, and regulatory activities.
What you'll do
- Coordinate and complete assigned trial activities according to task requirements.
- Review department, country, investigator, and trial files and document findings.
- Support site activation, feasibility, site selection, and regulatory submissions.
- Maintain clinical trial systems, databases, trackers, and study documentation.
- Process and transmit documents to clients, eTMF, and centralized IRB/IEC.
- Communicate with sites and clinical personnel about documents, issues, risks, and follow-up.
- Train new personnel in applicable processes and systems.
What you'll need
- High or secondary school diploma or equivalent with relevant formal academic or vocational qualification.
- 0–1 year of comparable experience.
- Ability to work independently and collaboratively while managing multiple tasks.
- Proficiency in MS Office, including Word, Excel, and PowerPoint.
- Knowledge of applicable country regulations, ICH Good Clinical Practices, and relevant SOPs.
- Good English and local-language skills as needed.
- Strong organization, communication, judgment, risk-management, and attention-to-detail skills.
Nice to have
Details
- Remote role in Colombia.
- Standard Monday–Friday schedule.
- Occasional travel and drives to site locations may be required.
- Work may occur in an office, laboratory, clinical, or home-office environment.
Read the full description and apply on the company’s own careers page.
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