CLINICAL RESEARCH COORDINATOR III - LYMPHOMA

Moffitt Cancer Center; Tampa (FL); On-site; USD 67,000 - 102,000; Full time

Job summary

Moffitt Cancer Center is seeking a Clinical Research Coordinator III to support the Lymphoma Data Management program. You will coordinate patient care with medical staff and ensure protocol compliance and regulatory requirements.

In this senior role, you’ll screen and enroll subjects, manage study workloads, and liaise with investigators, regulatory staff, and sponsors. Strong communication and organizational skills are essential for success.

Qualifications

• Bachelor’s degree with 4 years clinical trials coordination experience; or Associate’s with 6 years experience.
• CCRP/CCRC certification required.
• Proficiency in EMR/CTMS and data capture systems; strong understanding of Good Clinical Practices.

Responsibilities

• Coordinate clinical research activity for Lymphoma Data Management program.
• Screen, enroll, and follow study subjects while ensuring protocol compliance.
• Communicate with investigators, providers, regulatory staff, and sponsors.
• Provide guidance to junior team members and manage workload.

Skills

Communication

Interpersonal skills

Time management

Attention to detail

Education

Bachelor’s degree + 4 years experience

Associate’s degree + 6 years experience

Tools

EMR systems

CTMS

Data capture systems

Microsoft Office

Job description

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.SummaryMoffitt Cancer Center (MCC), an NCI-designated comprehensive cancer center in the state of Florida and ranked as one of Best Hospitals for Cancer on U.S. News & World Report, is seeking highly motivated individuals to join the Clinical Trials Office as a Clinical Research Coordinator III (CRC III) for the Lymphoma Data Management program.Be part of the significant contributions to the prevention and cure of cancer which is based on compassion for our patients, an emphasis on collaboration, and a culture of scientific excellence.The clinical research coordinator (CRC III) is the third level in the CRC career path and coordinates clinical research activity at Moffitt Cancer Center. Within the career path this is considered a fully functioning career level role, with high proficiency and is expected provide guidance to lower-level coordinators in CTO and MRI, as a subject matter expert.Clinical Research Coordinator IIIPosition Highlights:Determines methods and procedures on new protocol requirements while implementing good clinical practices as set forth by Federal regulations..As the primary resource for the protocols, the CRC III will coordinate patient care by collaborating with medical staff, and document in accordance with standards and regulatory guidelines.Will act as liaison between the investigators, care providers, Moffitt regulatory staff and the sponsor.Along with the investigator, the CRC III will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.The CRC III will perform all Clinical Research Coordinator core support and additional responsibilities as detailed for the Clinical Research Coordinator II with the expectation of ability to carry a higher study/patient workload.The CRC III is expected to work independently with moderate oversight and direction from the supervisor and Principal Investigator (PI), to implement and coordinate research, including administrative procedures. Moderate supervision with some latitude for independent judgment is provided Has limited problem-solving responsibility while working under defined guidelines.Normally receives little instructions on day- to-day work, with general instructions on new assignments.Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors.Demonstrates good judgment in selecting methods and techniques for obtaining solutions.Networks internally and externally in own area of expertise.Has in-depth conceptual and practical knowledge in own discipline and basic knowledge of related disciplines.Contributes to process improvements.Typically resolves complex problems or problems that do not have routine solutions.Acts as a resource for less experienced colleagues.Credentials and Qualifications:*Bachelor’s degree with 4 years of experience in clinical trials coordination*In lieu of a bachelor’s degree, Associate’s degree with 6 years clinical trials coordination experience may be consideredCCRP/CCRC certification requiredHigh proficiency in word processing (Microsoft Office Suite), data base entry, and through knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research.Should be proficient in the use of EMR systems, clinical trial management systems and other various data capture/reporting systems.Must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals.Highly proficient understanding of medical terminology required.Ability to work under little guidance to plan, organize, and coordinate multiple work assignments, establish and maintain effective working relationships with others in a team setting, act as a subject matter expert and communicate clearly verbally and in writing.Must have ability to 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.Salary Range$31.99 - $48.80Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.Moffitt Career SiteIf you have the vision, passion, and dedication to contribute to our mission,then we have a place for you!1. Equal Employment OpportunityMoffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.2. Reasonable AccommodationFederal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email at [e-mail]. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.Read more information about your EEO rights under the law.Transparency in Coverage Rule