CLINICAL RESEARCH COORDINATOR II - HEAD & NECK

Responsibilities

• Supporting the PI in clinical trials by implementing and coordinating research including administrative procedures at Moffitt Cancer Center
• Support PI sponsored IND or IDE trials
• Coordinate patient care by collaborating with medical staff, and document in accordance with standards and regulatory guidelines
• Act as liaison between the investigators, care providers, Moffitt regulatory staff and the sponsor
• Screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study
• Perform all CRC core support and additional responsibilities of more complex studies, with a higher patient volume in comparison to the CRC I
• Determining methods and procedures for the coordination of newly assigned studies
• Solves a range of straight forward problems using prescribed guidelines and policies
• Continues to build productive internal/external working relationships
• Plan, organize, and coordinate multiple work assignments, establish and maintain effective working relationships with others in a team setting and communicate clearly verbally and in writing
• Prioritize and pace one’s-self when working under the pressure of deadlines and work volume
• Successfully demonstrates competency by meeting established competency guideline/check list annually

Preferred

• Bachelor's Degree preferred
• CCRP/CCRC or equivalent
• Prior experience in an oncology setting is preferred

Benefits

• Hybrid (Part -time in Office)
• Glassdoor
• 3.9
• Moffitt Cancer Center are contribute to the prevention and cure of cancer.
• 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
• Medical Xpress - latest medical and health news stories
• Redesigned lung cancer drug matches tumor control with fewer off-target interactions

Qualifications

• Associate's Degree in a scientific, health related or business administration program required
• Two (2) years of experience in clinical trials coordination with a Bachelor's degree
• Four (4) years of experience in clinical trials coordination with an Associate's degree
• TheCRC II is required to have through knowledge of word processing (Microsoft Office Suite), database entry, and through knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research
• This person should be proficient in the use of EMR systems, clinical trial management systems and other various data capture/reporting systems
• The CRC must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals
• This person possesses a proficient understanding of medical terminology required
• The CRC II is required to work under minimal supervision to plan, organize, and coordinate multiple work assignments, establish and maintain effective working relationships with others in a team setting and communicate clearly verbally and in writing
• The person must have the ability to prioritize and pace one's-self when working under the pressure of deadlines and work volume
• Bachelor's Degree preferred
• CCRP/CCRC or equivalent
• Prior experience in an oncology setting is preferred

Required skills

• CCRP/CCRC Certification, Clinical Practice (GCP), Clinical Research, Clinical Trial Management Systems, Clinical Trials Coordination, Database Entry, Electronic Medical Records (EMR), Human Subjects Protection Regulations, Medical Terminology, Microsoft Office Suite, Oncology Research, Work Prioritization

Preferred skills

• Bachelor's Degree preferred, CCRP/CCRC or equivalent, Prior experience in an oncology setting is preferred

Experience

• 2-4 years