CRA 1 (Clinical Research)

Location: Must live in Bogota, Colombia; availability to travel is required.

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Conduct site selection, initiation, monitoring, and close-out visits according to the study protocol, GCP, ICH guidelines, and regulatory requirements.
• Support site recruitment plans, track enrollment, and manage ongoing communication with assigned sites.
• Provide protocol and study training, evaluate site practices, and escalate quality issues when necessary.
• Track regulatory submissions, approvals, CRF completion, data queries, and query resolution.
• Maintain site documentation, verify Investigator's Site Files, and ensure required records are filed in the Trial Master File.
• Prepare monitoring visit reports, follow-up letters, action plans, and other study documentation while collaborating with project team members.

Requirements

• Bachelor's degree in a scientific or healthcare discipline preferred.
• At least 1 year of on-site monitoring experience or 2–3 years of experience as a Study Coordinator.
• Must live in Bogota, Colombia and be available to travel.
• Good command of English in written and verbal communication is required.
• Knowledge of clinical research regulations, including GCP and ICH guidelines, plus therapeutic and protocol knowledge.
• Proficiency with Microsoft Word, Excel, PowerPoint, and applicable laptop, iPhone, and iPad tools.

Culture & Benefits

• Work with clinical research sites, study teams, clients, and healthcare stakeholders.
• Responsibilities include organizational, problem-solving, time-management, and financial-management activities.
• Employment is full time and involves field-based clinical trial monitoring.