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Last Updated: 3/31/17

Job Description

CLINICAL RESEARCH NURSE

Full Time Position/PT will be considered

Candidate will have overall responsibility for the following: Coordination and administration of clinical research protocols. Responsibilities includes protocol development and implementation, coordination of patient informed consents, compliance, preparation of regulatory documents for IRB submission, assisting with the submission of study data and federal reporting of adverse events, organization of study materials, recruitment, clinical care, and follow-up of research participants, and provide in-service teaching with physicians, nursing and support staff of protocol requirements and serve as liaison between Principal investigator and various study staff.

General Minimum Qualifications: Bachelors Degree required, Masters Degree preferred. Three (3) years of related experience.

Additional Specific Minimum Qualifications: Minimum of BSN with New York RN license; Will consider NP or PA

Preferred Qualifications: Plastic Surgery/Burn/Wound Experience, Extremely strong computer and communications skills; knowledge of protocols and data management experience, proven leadership qualities

Company Details

Carle Place, New York, United States
“To partner qualified spine professionals with career building and financially rewarding opportunities.” The SpineSearch mission is steadfast in providing a superior network between highly qualified healthcare professionals, spine specialists, and healthcare facilities. Our vision is to provide a cutting edge network within the spine field and its professionals. We are focused exclusively to the...