- Coordinates the recruitment efforts of clinical studies. Works closely with the research team to facilitate the outreach, enrollment, treatment and data collection of research subjects.
- Facilitates sample collection, processing, and storage activities, as required by protocols.
- Develops and maintains study documentation and databases. Performs data collection, entry, and analysis.
- Disseminates to investigators and/or program directors updated study documents.
- Compiles data reports and progress reports.
- Assists with research analyses for publications and presentations.
- Prepares materials for lectures and publications.
- Coordinates the data management of clinical trials in compliance with federal regulations and internal policies.
- Attends pertinent conferences and provides guidance to internal health care personnel regarding clinical trials.
- High School Diploma
- Candidate must have excellent communication and organizational skills and must be highly detailed oriented.
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Research Program Specialist - New York, United States - WCM-Q
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Description
Position Summary
Under general supervision, manages the development, management, and auditing of clinical research functions and programsJob Responsibilities
Education
Experience
Bachelor's degree is preferred.
Approximately 2 years of prior experience in a health-related clinical or research setting
Knowledge, Skills and Abilities
Licenses and Certifications
Working Conditions/Physical Demands
Standard office work