Clinical Research Coordinator: Drive Trials & Data

ALS; Purchase (NY); On-site; USD 60,000 - 85,000; Full time

Job summary

ALS is a global team dedicated to using scientific testing and data-driven insights to create a healthier future. The Clinical Research Coordinator will plan, coordinate, and execute clinical studies, manage data, and ensure compliance with approved protocols, SOPs, and current Good Clinical Practice guidelines.

Responsibilities include preparing study materials and documentation, obtaining informed consent, verifying eligibility, monitoring daily study activities, recording adverse events, and

Qualifications

• Coordinate and support planning, initiation, implementation, and day-to-day execution of clinical research studies in accordance with study protocols, sponsor requirements, SOPs, and Good Clinical Practice guidelines.

Responsibilities

• Prepare, organize, and maintain study materials and documentation, including informed consent forms, screening materials, medical history forms, source documents, study calendars, diaries, and sign-in sheets.
• Explain study procedures to participants, obtain informed consent, and verify eligibility criteria in collaboration with the Recruitment Department and study team.
• Monitor study activities to ensure efficient workflow, proper scheduling, and subject throughput while maintaining compliance with protocol requirements.
• Record adverse events and other study data accurately in study records and ensure data integrity across study datasets.
• Operate study-related instruments and equipment, download and maintain study data and images, and ensure proper shutdown and storage after use.

Skills

Clinical research coordination

GCP awareness

Data management

Job description

ALS is a global team dedicated to using scientific testing and data-driven insights to create a healthier future. The Clinical Research Coordinator will plan, coordinate, and execute clinical studies, manage data, and ensure compliance with approved protocols, SOPs, and current Good Clinical Practice guidelines.

Responsibilities include preparing study materials and documentation, obtaining informed consent, verifying eligibility, monitoring daily study activities, recording adverse events, and