Data Coordinator

About the Role

Key Responsibilities

• Coordinate and manage data entry for oncology treatment trials.
• Perform site initiation activities.
• Facilitate the comprehensive compilation of research patient records according to federal regulations, Good Clinical Practice, and institutional policies.
• Maintain the quality of research and address patient safety and regulatory compliance.

Requirements

• Bachelor's degree or equivalent combination of training and experience from an accredited institution.
• Knowledge of ICH GCP, Federal Regulations and Guidelines, and ability to follow established regulations, procedures, and protocols.
• High level of accuracy and attention to detail.
• Strong computer skills.
• Ability to gather data and document procedures.
• Ability to plan work and coordinate multiple projects.
• Ability to contribute to preparation and delivery of reports, trainings, and SOPs.
• Customer-oriented with the ability to work in a team environment.
• Effective and professional verbal and written communication skills.
• Ability to work on evenings, weekends, and/or holidays occasionally required.

Nice to Have

• Previous experience with therapeutic clinical research involving drugs and/or devices.
• Experience in Phase I, II, and III clinical research.
• Experience navigating medical records and data extraction.
• One year of data coordinator experience or experience in oncology clinical trials.

Qualifications

• Experience in oncology clinical trials or related data coordination roles.

Benefits & Perks

• Not specified in the description.