MYEOMA & LYMPHOMA RESEARCH DATA COORDINATOR III

Moffitt Cancer Center; Tampa (FL); On-site; USD 51,000 - 78,000; Full time

Job summary

Moffitt Cancer Center is seeking a Research Database Coordinator III to manage protocol-specific data for diverse clinical trials. The role requires reviewing medical records and extracting data for industry, cooperative, and investigator-initiated trials.

You will use EMR and clinical trial management systems, maintaining data integrity and confidentiality while collaborating with physicians and staff across departments.

Qualifications

• Associate's Degree preferred; High School Diploma/GED may be considered with 4 years of experience.
• Must have training in Clinical trial management systems and EMR systems.

Responsibilities

• Review and synthesize information from medical records to extract trial data as per protocols.
• Ensure data requirements align with good clinical practice and federal regulations.
• Work independently with coordinators and monitors and resolve data queries with minimal guidance.

Skills

EMR systems

Clinical trial management systems

Data management

Verbal and written communication

Education

Associate's Degree

Tools

EMR systems

Clinical trial management systems

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.SummaryThe Research Database Coordinator III (RDC III) is a highly skilled role responsible for protocol specific data requirements for multiple, diverse and complex research projects, while ensuring data requirements are in alignment with good clinical practice according to Federal regulations. The RDC performs core support and additional responsibilities including higher patient volume and/or higher trial complexity.Research Data Coordinator IIIThe Research Database Coordinator III (RDC III) is a highly skilled role responsible for protocol specific data requirements for multiple, diverse and complex research projects, while ensuring data requirements are in alignment with good clinical practice according to Federal regulations. The RDC performs core support and additional responsibilities including higher patient volume and/or higher trial complexity. Workload is more complex and comprehensive and the RDC works independently maintaining the highest level of expertise to review and synthesize information from medical records (clinic notes, pathology reports, radiology reports, patient questionnaires, etc.) to extract industry, cooperative, and investigator-initiated trial data as specified by assigned research protocols. The Research Data Coordinator (RDC) III is the third level in the data coordinator career path.Requirements:Minimum EducationAssociate's Degree preferred; High School Diploma/GED may be considered*In lieu of an Associate's Degree, a High School diploma/GED with Four (4) years of research data management experience may be consideredPreferred Licensure: SOCRA/ACRP or equivalentMinimum Experience:Two (2) years of research data management experienceTraining Required: Clinical trial management systems and electronic medical record (EMR) experience required. In this senior role, the incumbent understands the implications of the work and makes recommendations for solutions, while completing tasks in resourceful and effective methods. The position performs assigned tasks independently and works autonomously with coordinators and the monitors. It resolves data queries without routine guidance and provides assistance in completion of various source documents. This person must possess highly effective verbal and written communication skills as well as excellent interpersonal skills with staff and other health care professionals. They must have ability to prioritize and pace one’s-self when working under the pressure of deadlines and high work volume. They will successfully demonstrate competency by meeting established competency guideline/check list annually. The person should be an expert in the use of EMR systems, clinical trial management systems and other various data capture/reporting systems. They must be able to interpret all components of the medical record and maintain confidentiality requirements as well as security of subject data. Excellent oral and written communication skills are needed. They must be comfortable talking to physicians and other health care professionals as well as training other data coordinators. The person works independently under minimal supervision from their Manager/Supervisor.Salary Range$24.45 - $37.31Salary 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