Clinical Research Job at IQVIA, Colombia | Life Sciences | Apply Now
If you are an early-career professional looking to enter the clinical trials sector with a global industry leader, this position at IQVIA is an exceptional opportunity. Located in Bogotá, Colombia, this hybrid role places you at the operational core of the local clinical operations unit. For structured coordinators searching for a high-impact Clinical Research Job, this position offers an ideal environment to master international trial administration and database tracking. It serves as an excellent launchpad for a long-term IQVIA Career and stands out as a premier Life Sciences Job in Latin America.
- Job Position: Clinical Trial Assistant (CTA)
- Location: Bogota, Colombia
- Job ID: R1548649
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. The company focuses on creating intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. By building an IQVIA Career, you join a high-performance global community that actively invests in workplace inclusion and values diversity as a core driver of medical innovation.
Clinical Research Job – Key Responsibilities
As a Clinical Trial Assistant (CTA), you will provide critical administrative and operational support to project teams, ensuring all clinical trial activities comply with ICH-GCP guidelines and internal standard operating procedures.
Your day-to-day administrative and coordination duties will include:
- Documentation Management: Organizing, maintaining, and verifying regulatory documentation and essential files within the Trial Master File (TMF) framework to advance this Clinical Research Job.
- Systems & Database Tracking: Updating internal clinical trial databases, systems, and tracking tools with study-specific metrics and site data.
- Cross-Functional Coordination: Handling administrative and logistical coordination between local site monitors and global project management teams.
- Operational Logistics: Managing calendars, arranging study-related meetings, distributing critical communications, and handling logistics for trial supplies.
- Regulatory Compliance Support: Assisting the wider clinical operations unit in tracking site startup milestones, regulatory approvals, and protocol compliance indicators to optimize this Life Sciences Job.
Qualifications & Requirements For Clinical Research Job
This position is tailored for highly organized professionals who demonstrate a meticulous approach to data verification and a collaborative mindset.
- Educational Foundation: A university degree in Life Sciences, or a closely related academic field is preferred.
- Professional Experience: 1+ years of experience in clinical research, healthcare administration, or corporate project support environments.
- Linguistic Fluency: Advanced English proficiency (both written and verbal) is required to collaborate effectively with global cross-functional teams.
- Technical Software Skills: Solid proficiency in Microsoft Office tools, particularly Excel, with an aptitude for learning specialized clinical databases.
- Core Competencies: Strong organizational habits, exceptional attention to detail, robust teamwork skills, and the capacity to handle confidential information ethically.
- Logistics & Schedule: Full-time, hybrid work model based out of the Bogotá, Colombia office.
In short, the Clinical Trial Assistant position at IQVIA in Bogotá is a definitive route to transitioning your educational background or early clinical experience into a corporate trial management path. Securing this role allows you to build highly marketable skills in international GCP auditing, database tracking, and global study logistics. If you possess a sharp eye for document compliance and speak fluent English, apply today to secure this premier Clinical Research Job and fast-track your IQVIA Career.
