Description

You will manage clinical research activities to ensure accurate data collection within established timelines. You own the end-to-end study execution, from patient recruitment to final data validation.

Responsibilities

• Manage research activities, tracking budgets, study milestones, and deadlines.
• Recruit and enroll eligible patients, manage scheduling, and complete Case Report Forms (CRFs).
• Select and manage vendors and CROs, including Central Lab, IVRS, and EDC providers.
• Review and evaluate medical data in accordance with ICH GCP guidelines and local regulations.
• Participate in study audits and manage IRB procedures and processes.

Required Skills

• Minimum 2 years of experience in a clinical research coordinator role.
• Expertise in ICH GCP guidelines and clinical trial research processes.
• Experience with IRB procedures, data management, and CRF completion.
• Proven ability to manage vendors and CROs.
• Strong analytical, organizational, and multitasking skills.
• Ability to solve complex problems and prioritize multiple tasks proactively.

Preferred Skills

• Degree in medicine, science, health, or an equivalent field.

Key Skills

Education

ANY GRADUATE