FEATURED PROJECT: Medical Research CSR- $22 hr.
SALARY RANGE: $ 22 Salaried
HOURS: Part time, and F/T hours
We are searching for Data Coordinators and Collectors. The Data Coordinator and Collectors are 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.
Nationwide Oncology delivers high-quality, high-touch care to help cancer patients achieve “More breakthroughs. More victories.” in their fight against cancer. We are an independent, physician-led practice delivering leading-edge technology and treatment options and conducting innovative research.
With more than 350 sites of service throughout the U.S., with more than 225 physicians dedicated to serving our patients. On average, we treat more than 85,000 new cancer patients each year, with documented growth year over year. We give local communities access to leading-edge technology that was previously only available in larger metropolitan areas.
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.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
-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 online screening patients for potential study enrollment.
-May assist with patient online 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 for individual offices or regions.
-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.
High school diploma or equivalent required; some college coursework other relevant background preferred. Requires 0-3 years experience. Some medical office experience required, preferably in oncology. Knowledge of medical terminology required.
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of an office based position and may not be for this job specifically. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to experience prolonged sitting, some bending, stooping and stretching. Requires eye-hand coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator and other office equipment.
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is exposed to conditions typical in a medical office setting.
Our mission is to provide excellent, evidence-based care for each patient we serve, while advancing cancer care for tomorrow. To this end, we give patients access to the highest quality cancer care available today within their own local communities. Our cutting-edge technologies, treatments and research are offered in welcoming and comfortable environments. We maintain comprehensive quality oversight and responsible financial management. At all times, we pride ourselves in being moral, ethical and efficient as a medical practice and employer.
We extend an extremely competitive offering of benefits to employees, including Medical Health Care, Dental Care, Vision Plan, 401-k with a matching component, Life Insurance, Short-term and Long-term disability and Wellness & Perks Programs.
Come join our growing organization and enjoy knowing that you work for an organization dedicated to making the lives of others better.
The US Oncology Network is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.
DO NOT CALL, Resume Portfolio / VA Websites will be reviewed online and applicants will be contacted directly. Must have VOT resume profile and website available for review
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We look forward to working with you.