We're looking for a Clinical Research Associate, working in the Pharmaceuticals & Medical Products industry in Des Plaines, Illinois, United States.
Assists senior staff in planning study conduct, designs case report forms (CRFs), Contract Research Organization (CRO) selection and management, selects and trains of investigator sites.
Authors basic study protocols, monitors or oversees monitoring of investigational sites.
Ensures protocol adherence, assures timely enrollment of patients and retrieval of CRFs from study sites, processes CRFs including data cleanup and classification of data, and completion of study summary.
The pay range we're offering is 30 - 35 per hour. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
3-5 years of relevant clinical trial monitoring experience
IVD and oncology experience highly preferred, but not required
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.