- 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
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Research Coordinator
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Catholic Health Service West Islip, United StatesOverview 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 involve ...
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Research Coordinator
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Albert Einstein College of Medicine Bronx, United StatesSpecifically, the Coordinator will:Work with PI to develop study protocols and protocol amendments for the IRB as needed, including the development of new measures. Manage subject accrual, enrolment and retention, including advertising and outreach. Research Coordinator, Research ...
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Research Coordinator
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Research Program Coordinator
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Research Program Coordinator
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Stony Brook University Commack, United StatesJob Description - Research Program Coordinator - Commack/Westbury · Research Program Coordinator - Commack/Westbury · Required Qualifications (as evidenced by an attached resume): · Bachelor's degree (foreign equivalent or higher) in Social Sciences, Public Health, or a related ...
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Research Program Coordinator
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Stony Brook Medicine Commack, United StatesRequired Qualifications (as evidenced by an attached resume): Bachelor's degree (foreign equivalent or higher) in Social Sciences, Public Health, or a related field in hand by May 2024. Experience working in a research setting. Preferred Qualifications: Experience coordinating a ...
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Northwell Health Huntington, United StatesJob Description · Coordinates and monitors research trials; actively oversees the recruitment of study participants. May be required to perform venipuncture on study participants; collects, processes, and ships specimens according to protocol and training requirements. Adheres t ...
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Danbury Health Systems Norwalk, United StatesClinical Research Coordinator, Norwalk, CT · Full-time, 40 hours; 8:30 am - 5:00 pm · Nuvance Health has a network of convenient hospital and outpatient locations - Danbury Hospital, New Milford Hospital, Norwalk Hospital and Sharon Hospital in Connecticut, and Northern Dutchess ...
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Clinical Research Coordinator
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Nuvance Health Norwalk, United StatesClinical Research Coordinator, Norwalk, CT · Full-time, 40 hours - 8:30 am - 5:00 pm · Nuvance Health has a network of convenient hospital and outpatient locations - Danbury Hospital, New Milford Hospital, Norwalk Hospital and Sharon Hospital in Connecticut, and Northern Dutchess ...
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Medix™ East Northport, United StatesDuration: · 4 month contract · Schedule: · 24 hours per week (Monday, Wednesday, Friday 8AM-5PM EST) · Location: · 11731 · Responsibilities: · Supporting a registry study in both clinical (phlebotomy, EMR, etc) and non clinical capacities. · ...
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Clinical Research Coordinator
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Northwell Health Manhasset, United StatesJob Description · Job Description · Coordinates and monitors research trials; actively oversees the recruitment of study participants. May be required to perform venipuncture on study participants; collects, processes, and ships specimens according to protocol and training requ ...
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Medical Research Coordinator
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New York Cancer & Blood Specialists Shirley, United StatesMedical Research Coordinator · Shirley, NY · New York Cancer and Blood Specialists (NYCBS), a prominent and respected Oncology/Hematology group, is seeking a Research Coordinatorto join a well-established and growing pure sub-specialty practice with academic affiliation. Clini ...
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Medical Research Coordinator
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Clinical Research Coordinator
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Northwell Health Manhasset, United StatesJob DescriptionJob DescriptionCoordinates and monitors research trials; actively oversees the recruitment of study participants. May be required to perform venipuncture on study participants; collects, processes, and ships specimens according to protocol and training requirements ...
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Clinical Research Coordinator
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Medix™ Setauket- East Setauket, United StatesDuration: · 1-4 month contract · Schedule: · 40 hours per week (Monday through Friday 8AM-5PM EST) · Location: · 11733 · Responsibilities: · Patient recruitment · Community outreach · Data Entry into EDC · ...
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Clinical Research Coordinator
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IQVIA, Inc. Bronx, United StatesAre you looking for your next opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression? If so, come and join us · We are looking for experienced candidates to perform a vari ...
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Clinical Research Coordinator
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IQVIA Bronx, United StatesAre you looking for your next opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression? If so, come and join usWe are looking for experienced candidates to perform a variety ...
Research Coordinator - West Islip, United States - Catholic Health Service
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 Details:Responsibilities:
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 candidates 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.
