NE-CRADLS - CLINICAL RESEARCH ASSOCIATE-Dallas, TX
Looking for a Clinical Research Associate to assume monitoring
responsibilities of clinical trial sites, and to develop study monitoring
procedures and study management tools.
Main duties and responsibilities:
1. Manage study start-up activities (input in protocol development,
development of Informed Consent Forms, Case Report Forms, and related study material)
2. Develop and implement innovative approaches for site recruitment,
selection and initiation activities.
3. Conduct periodic clinical site monitoring visits to ensure the integrity
of clinical data and to ensure proper storage, dispensation and
accountability of clinical trial materials, according to applicable
regulatory, protocol, and company guidelines
4. Maintain patient tracking records for assigned sites and/or studies.
5. Conduct study close-out visits.
6. Help prepare final study reports and compile submissions to Regulatory
Authorities.
Qualifications:
BA/BS or MS in Biological Sciences, RN or health related field, and a minimum of 1-5 years of monitoring experience.
Experience in oncology trials preferred.
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