Posted 5 months ago

Job Features

Roles and ResponsibilitiesResponsible for assisting with the selection, initiation, regular monitoring and closeout of investigative sites. Requires flexibility, excellent interpersonal skills, previous industry experience, and the ability to work well with all levels of staff, as well as outside clients and vendors. Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data is a must. Sensitivity to confidential matters is required.
EducationBachelors Degree of higher
Qualifications3+ years of relevant experience as a Clinical Research Associate
Preferred ExperienceMedical Device and/or Diagnostic Trials, Detail Oriented, Excellent Communication Skills
Job TypeFull Time
SalaryCompetitive, DOE
BenefitsFlexible Schedule, Health Insurance, Employer 401(k) Match

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