CLINICAL RESEARCH COORDINATOR I - CUTANEOUS

Moffitt Cancer Center is hiring a Clinical Research Coordinator I to coordinate therapeutic cancer clinical trials and support safe, compliant study conduct. The role involves coordinating patient care, screening and following study participants, and managing study documentation and communications with investigators, regulatory staff, and sponsors.

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
• CCRP/CCRC Certification
• Equivalent

Benefits

• Monday through Friday schedule and 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 two (2) years of relevant clinical, health related, scientific, business or research experience
• CCRP/CCRC or equivalent
• 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 two (2) years of relevant clinical, health related, scientific, business or research experience

Required skills

• CCRC, CCRP

Preferred skills

• CCRP/CCRC or equivalent

Experience

• 1+ years