- Coordinate and implement procedures to enroll research subjects, collect data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources; code, evaluate and interpret collected data and prepare appropriate documentation.
- Ensure compliance with protocol guidelines and requirements of regulatory agencies; identify problems and/or inconsistencies and monitor patients' progress to include documentation and reporting of adverse events; recommend corrective action as appropriate.
- Evaluate and interpret collected clinical data in conjunction with principal investigator(s) as appropriate; prepare oral presentations or written reports and analyses setting forth progress, trends and appropriate recommendations or conclusions.
- Confer with principal investigator(s) to assist in developing plans for research projects and to discuss the interpretation of results; collaborate on the preparation of manuscripts for publication.
- Coordinate the development of forms, questionnaires and the application of research techniques; assist in writing procedures manuals for data collection.
- Review journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies.
- Partners with PI, research team and clinical team to identify if patient (s) meet eligibility for clinical trial
- Completion of a bachelor's degree in a field related to health science with a strong interest in clinical research or relevant experience within Oncology
- ACRP or CCRP preferred
- Basic computer skills required ( Word, excel)
- Excellent verbal communication and customer service skills; must be detailed oriented and be able to work independently.
- Medical related field or education background. Oncology and/or research experience preferred.
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Research Coordinator - West Islip, United States - St. Catherine of Siena
Description
Overview
The Clinical Cancer Research Coordinator coordinates and participates in clinical research studies conducted by principal investigator(s) at the Cancer Center at Good Samaritan Hospital Medical Center.
Coordinate and participate in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data.
Job DetailsResponsibilities:
Requirements:
USD $ USD $36.75 /Hr.
This range serves as a good faith estimate and actual pay will encompass a number of factors, including a candidate's qualifications, skills, competencies, and experience and position location.
The salary range or rate listed does not include any bonuses/incentive, differential pay or other forms of compensation that may be applicable to this job and it does not include the value of benefits.
At Catholic Health, we believe in a people-first approach.In addition to the estimated base pay provided, Catholic Health offers generous benefits packages, generous tuition assistance, a defined benefit pension plan, and a culture that supports professional and educational growth.
