Clinical Research Coordinator

Responsibilities

• Coordinate and support the planning, initiation, and day-to-day execution of clinical research studies in accordance with study protocols and Good Clinical Practice guidelines.
• Prepare and maintain essential study documentation, including informed consent forms, medical history forms, and source documents.
• Explain study procedures to research participants and obtain informed consent while ensuring subject eligibility.
• Prepare study areas, test materials, and supplies required for study conduct.
• Monitor research subjects' responses, document observations, and accurately record adverse events and study data.
• Operate study-related instruments and equipment, ensuring proper data collection and documentation.
• Maintain study files and administrative records in an inspection-ready condition.
• Collaborate with investigators, project managers, and internal departments to communicate study progress and support reporting.

Requirements

• Bachelor's degree from a 4-year university.
• 1–2 years of experience in the clinical industry (can be used as a substitute for a BS or BA).
• Proficient computer skills.

Preferred Qualifications

• Bachelor of Science or Arts degree in life sciences.
• Current certification in Human Protections.
• Current certification in Good Clinical Practices (GCP).
• Current certification in Bloodborne Pathogens.

About the Company

ALS is a global leader in testing, providing comprehensive testing solutions to clients in a wide range of industries around the world. With over 20,000 team members across 70 countries, we use advanced technologies and innovative methods to help our clients leverage data-driven insights for a safer and healthier world.