North Chicago, Illinois, Illinois
Martinez, California, California
Durham, North Carolina
Nashville, Tennessee
Posted: 27-Sep-24
Location: Los Angeles, California
Salary: Open
Categories:
Internal Number: 142910563
The Study Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. You will be responsible for the implementation of research activities for one or more studies. The Study Coordinator recognizes and performs necessary tasks to manage projects and prioritizes work to meet necessary deadlines. You are responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). You will collaborate with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to compliant conduct, financial management, and adequate personnel support.
Salary Range: $33.63 - $54.11/Hourly
All Required:
- Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience.
- Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.
- Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.
- Analytical skills sufficient to address problems and identify solutions with reasoned judgment.
- 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.
- Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.
- Ability to handle confidential material with judgement and discretion.
- Working knowledge of the clinical research regulatory framework and institutional requirements.
- Mathematical skills sufficient to prepare clinical research budgets.
- Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
- Available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.
