Clinical Research Coordinator I - GI / Head & Neck

Responsibilities

• Coordinate patient care by collaborating with medical staff and document in accordance with standards and regulatory guidelines with direction of a mentor or supervisor
• Act as liaison between the investigators, Moffitt regulatory staff and the sponsor. • Will assist to screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study
• Responsible for data and source documentation and adverse experience reporting
• Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol
• Will work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures

Preferred

• CCRP/CCRC or equivalent preferred

Benefits

• Hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period.
• Paid training and orientation through Moffitt's CTO (Clinical Trials Office) Academy.
• Relocation assistance may be provided.
• Glassdoor
• 3.9
• Comprehensive cancer hospital and research center.
• Tampa, Florida, USA
• http://moffitt.org
• Late Stage
• Total Funding
• $0.01M
• Key Investors
• Foundation Medicine
• MassMutual Foundation
• 2023-07-31
• Grant
• 2023-07-12
• Grant· $0.01M
• Leadership Team
• Joanna Weiss
• Chief Financial Officer
• Timothy Yeatman
• Executive Vice President, Founding Chief Scientific Officer
• Recent News
• BioSpace
• Anixa Biosciences Announces First Case of Stable Disease for Three Months in Ovarian Cancer CAR-T Clinical Trial
• 2026-10-06
• Morningstar.com
• Cizzle Bio Highlights CIZ1B Biomarker Blood Test for Lung Cancer at Next Generation Dx Summit
• 2026-08-26

Qualifications

• Bachelor's degree (preferred field of study scientific, health related or business administration program) with one (1) year of relevant clinical, health related, scientific, business or research experience
• In lieu of bachelor's degree, Associate's degree with 2 years of relevant clinical, health related, scientific, business or research experience
• CCRP/CCRC or equivalent preferred
• Bachelor’s degree (preferred field of study scientific, health related or business administration program) with one (1) year of relevant clinical, health related, scientific, business or research experience
• In lieu of bachelor’s degree, Associate’s degree with 2 years of relevant clinical, health related, scientific, business or research experience

Required skills

• Clinical Research, Clinical Trial Coordination, Clinical Trial Protocol Compliance, Patient Enrollment, Clinical Data and Source Documentation, Adverse Event Reporting, CCRP/CCRC Certification

Preferred skills

• CCRP/CCRC or equivalent preferred

Experience

• 1+ years