Clinical Research Coordinator

Overview

• Coordinate clinical research studies ensuring compliance with protocols and regulations.
• Collaborate with site teams to execute study-related activities effectively.
• Perform patient screening, consent, and follow-up visits for enrollment.
• Document patient data in electronic systems and resolve queries promptly.
• Conduct basic lab procedures, including specimen collection and shipping.
• Maintain study logs, charts, and order study-specific supplies as needed.
• Assist with study start-up activities, training, and technology setup.
• Ensure confidentiality and compliance with HIPAA guidelines.

Key Responsibilities & Duties

• Screen and enroll patients for clinical research studies following protocols.
• Perform clinical procedures such as vitals, ECGs, and phlebotomy.
• Document and report adverse events and deviations to sponsors and IRBs.
• Prepare and attend site initiation visits and investigator meetings.
• Maintain effective communication with clients, team members, and stakeholders.
• Update and manage study-specific logs and patient records accurately.
• Conduct monitoring visits and resolve issues in a timely manner.
• Assist with recruitment and tracking of study participants.

Job Requirements

• Associate’s degree or equivalent combination of education and experience required.
• Minimum 1 year of clinical research or clinical experience required.
• Proficiency in basic clinical procedures such as vitals and phlebotomy preferred.
• Strong organizational skills and attention to detail essential.
• Proficiency with Microsoft applications and electronic health records required.
• Ability to handle sensitive information confidentially and professionally.
• Bilingual proficiency in English and Spanish is a plus.
• Effective communication and interpersonal skills are necessary.