Clinical Research Scientist


Assists clinical trial leader or may act as clinical trial leader in the management of individual clinical trials. Under the direction of the clinical trial leader or clinical research manager, conducts day-to-day activities including protocol writing, trial administration, report writing and interactions with other line units in support of clinical trials.

SKILLS

Contributes to continuous improvement of process, Contributes in preparing clinical trial protocol summaries and clinical trial protocols. Contributes in preparation and implementation of project specific training programs and training materials for internal and external staff. Contributes in monitoring safety, eligibility, enrollment and data consistency. Contributes in preparing draft clinical trial reports and draft summaries.

EDUCATION

BA required, with 3-5 years of experience required.