Indianapolis, Indiana
Wilmington, Delaware
Minneapolis, Minnesota
Allentown, Pennsylvania
Bethlehem, Pennsylvania
Posted: 08-Sep-24
Location: Los Angeles, California
Salary: Open
Categories:
Internal Number: 142197461
The Department of Medicine is seeking to hire a Clinical Research Coordinator in the Division of Nephrology to oversee and manage clinical research activities throughout the entire research study and trial process, from design and setup to execution and closeout. In this role, you will implement and oversee research tasks for one or more studies, ensuring project management, and meeting deadlines. You will be responsible for planning and organizing tasks to adhere to study protocols and relevant regulations, such as institutional policies, FDA CFR, and ICH GCP. Additionally, you will closely collaborate with the Principal Investigator, various departments, research teams, sponsors, and institutions to support all aspects of the studies, including compliant conduct, financial management, and personnel support.
Target hourly rate: $33.63-$54.11
- Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.
- Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience.
- Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.
- Ability to respond to situations in an appropriate and professional manner.
- Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.
- Ability to be flexible in handling work delegated by more than one individual.
- Ability to navigate numerous software programs and applications.
- Ability to handle confidential material information with judgement and discretion.
- Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.
- Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
- Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.
- Working knowledge of the clinical research regulatory framework and institutional requirements.
