Data Coordinator
2 months ago
Welcome We're excited you're considering an opportunity with us To apply to this position and be considered, click the Apply button located above this message and complete the application in full. Below, you'll find other important information about this position. This position will be responsible for the collection, validation, and entry of data using established tools, technology and databases. The Research Data Coordinator will perform data-related functions in order to support the accomplishment of the research/project objectives for a variety of clinical trials and/or studies. Coordinates and manages data registry-type clinical trials/protocols within the Department ensuring adherence to protocol requirements and regulatory guidelines. Is responsible for the collection, coordination, processing and quality control of clinical trial data. May assist with screening patients for research protocols. Obtains informed consent from subjects on data registry-type trials. Maintains research protocol information, regulatory documents and other research files as applicable. Works in compliance with principles of Good Clinical Practice and all applicable federal, state, and local regulations. MINIMUM QUALIFICATIONS: EDUCATION, CERTIFICATION, AND/OR LICENSURE: 1. Bachelor's Degree. EXPERIENCE: 1. Three (3) years' experience in research, administrative, or clinical support. PREFERRED QUALIFICATIONS: EDUCATION, CERTIFICATION, AND/OR LICENSURE: 1. Obtain certification as a Research Professional through the Society of Clinical Research Associates (SoCRA)ORthe Association of Clinical Research Professionals (ACRP) with three years of hire date. EXPERIENCE: 1. Three (3) years' experience in research or clinical support. CORE DUTIES AND RESPONSIBILITIES:The statements described here are intended to describe the general nature of work being performed by people assigned to this position. They are not intended to be constructed as an exhaustive list of all responsibilities and duties. Other duties may be assigned. Extrapolates data, completes case report forms, and ensures timely data submission. Coordination of data registry-type clinical trials, including scheduling follow up visits and testing, assessing subject response and review of laboratory data. Utilizes Clinical Trial Management System (CTMS) to access research forms and keep current all applicable patient reporting and tracking functions. Consent and Assent Forms and Discussion for data registry-type clinical trials. 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 sponsor requirements. Reviews the data collection forms for completeness and reconciles missing data for data entry. Collaborates with Clinical Research Specialists in screening... For full info follow application link. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities. Please view Equal Employment Opportunity Posters provided by OFCCP here. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c)
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