Date Coordinator (Clinical Research)

The US Oncology Network - Ocala, FL3.5

30+ days agoFull-time
Position Summary
Florida Cancer Affiliates is seeking a Full Time, Data Coordinator for our Clinical Research Dept. in our busy Ocala office. This position offers a great benefits package, medical, dental, vision, 401k and TOWP. Great research team to work for looking for someone who is outgoing, dedicated, hard working. Some medical office experience required, Oncology preferred. Knowledge of medical terminology is required.

Scope:
Under general supervision, is responsible for the collection, coordination, processing and quality control of clinical trial data. May assist with screening patients for research protocols. Maintains research protocol information, regulatory documents and other research files as applicable. Works in compliance with US Oncology Research (USOR) Standard Operating Procedure (SOP), principles of Good Clinical Practice and all applicable federal, state, and local regulations. Supports and adheres to the US Oncology Compliance Program to include the Code of Ethics and Business Standards.

Duties :
Extrapolates data, completes case report forms, and ensures timely data submission in accordance with USOR SOP.
Utilizes USOR Clinical Trial Management System (CTMS) to access research forms and keeps current all applicable patient reporting and tracking functions.
Actively prepares for and participates in monitoring and auditing activities. Assists in ensuring that all queries are resolved in a timely manner in accordance with USOR SOP and sponsor requirements.
Responsible for processing, filing and maintaining protocol regulatory documents.
May assist with screening patients for potential study enrollment.
May assist with patient scheduling for procedures required to maintain protocol compliance.
May assist with coordinating patient follow-up visits and timely data submission.
May assist with collection and processing of specimens, imaging documents, or other items required for research purposes.
May assist with ordering and maintaining research supplies.
May assist in the investigational drug accountability process.
Maintains research records in a confidential manner according to practice policies, sponsor confidentiality agreements, HIPAA guidelines and any other applicable regulations.

Category: ADMIN

The US Oncology Network is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability or protected veteran status.