Clinical Research Coordinator I - Myeloma/Lymphoma

Moffitt Cancer Center is a cancer research and treatment organization dedicated to contributing to the prevention and cure of cancer. The Clinical Research Coordinator I will coordinate clinical trial activities, interact with and support patients, and help ensure studies proceed safely, smoothly, and according to protocol. The role involves patient screening and enrollment, regulatory liaison work, data and source documentation, adverse experience reporting, and administrative research coordination.

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
• CCRP/CCRC Certification

Benefits

• Hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period.
• Paid training and orientation through its CTO (Clinical Trails Office) Academy.
• Relocation assistance may be provided.

Company

• Comprehensive cancer hospital and research center
• Tampa, Florida, USA
• http://moffitt.org/
• Founded in 1986
• 10001+ employees

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

Preferred skills

• CCRP/CCRC or equivalent preferred

Experience

• 1+ years