Clinical Research Coordinator I – Myeloma/Lymphoma

Moffitt

. Coordinate patient care by collaborating with medical staff and document according to standards and regulatory guidelines under direction of a mentor or supervisor .

Posted 9/22/2026full-timeTampa • Florida • United StatesJuniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in coordinating patient care, ensuring protocol compliance, and managing clinical research documentation. Proficient in collaborating with medical staff and regulatory bodies while adhering to standards and guidelines.

Highest-signal resume keywords

Clinical Research CoordinationProtocol CompliancePatient Care CoordinationData ManagementCCRP/CCRC Certification

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchData ManagementSource DocumentationAdverse Experience ReportingStudy Protocol Knowledge

Soft Skills

Analytical SkillsSound JudgmentCollaboration

Certifications & Qualifications

CCRPCCRC

Industry Keywords

Patient CareRegulatory GuidelinesClinical TrialsResearch AdministrationStudy Enrollment

About the role

Key responsibilities & impact

Coordinate patient care by collaborating with medical staff and document according to standards and regulatory guidelines under direction of a mentor or supervisor
Act as liaison between investigators, Moffitt regulatory staff, and sponsors
Assist to screen, enroll, and follow study subjects while ensuring protocol compliance and close monitoring
Manage data and source documentation and adverse experience reporting
Perform administrative duties requiring analysis, sound judgment, and knowledge of study protocol
Implement and coordinate research, including administrative procedures, under general supervision and direction from the supervisor and Principal Investigator

Requirements

What you’ll need

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
Ability to coordinate patient care and document according to standards and regulatory guidelines
Ability to screen, enroll, and follow study subjects while ensuring protocol compliance
Knowledge of study protocols and clinical research administrative procedures

Benefits

Comp & perks

Paid training and orientation through Moffitt’s Clinical Trials Office (CTO) Academy
Monday through Friday schedule
Hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period
Relocation assistance may be provided