TIME Clinical Research Coordinator
Cincinnati
Posted on 7/19/2023
INACTIVE
AI-driven precision medicine through clinical and molecular data analysis
Company Overview
Tempus Labs, Inc. is a leader in precision medicine, leveraging artificial intelligence to analyze vast clinical and molecular data, enabling physicians to deliver personalized, data-driven care. The company's advanced machine learning platform and unique solution sets facilitate the discovery, development, and delivery of optimized therapeutic options for patients. With a focus on extensive molecular profiling, Tempus has developed a robust pan-cancer tumor organoid platform and validated a liquid biopsy assay, demonstrating their commitment to transforming personalized patient care and their position at the forefront of the healthcare industry.
AI & Machine Learning
Data & Analytics
Company Stage
Series G
Total Funding
$1.3B
Founded
2015
Headquarters
Chicago, Illinois
Growth & Insights
Headcount
6 month growth
↑ 6%1 year growth
↑ 26%2 year growth
↑ 49%Locations
Cincinnati, OH, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Communications
PowerPoint/Keynote/Slides
CategoriesNew
Biology & Biotech
Requirements
- Candidate must have a Bachelor's degree in science or health related field
- 2+ years of work as a clinical research coordinator in an oncology setting
- CCRC preferable
- Strong planning and project management skills, with the ability to set goals and prioritize/manage multiple projects and tasks
- Excellent organization and communication skills with high attention to detail
- Knowledge of current FDA regulations, and Good Clinical Practices (GCP's) governing clinical research and HIPAA
- Proficient in the use of MS Office applications (Outlook, Word, Excel, PowerPoint)
- Understanding of study start up and trial activation
Responsibilities
- Educate and provide updates to providers and research staff regarding available TIME Trials and enrollment status
- Manage rapid study activations for just-in-time trials and oversee activities including but not limited to: collect and submit documents needed to initiate the study, prepare IRB submission, schedule SIV, organize and work with necessary hospital staff to complete all study related training
- Recruit and screen potential study participants and perform intake assessments for assigned trials
- Coordinate all study visits and assist PI with completion of trial activities including but not limited to: schedule participant visits, coordinate participant travel and meals, participant dosing and observation, scheduling and other evaluations, AE monitoring, vitals collection, and IVRS management
- Manage the inventory of equipment and supplies related to assigned trials
- Collect, process, and ship specimens
- Input data and patient information into electronic systems
- Ensure compliance with research protocols by providing ongoing quality control audits
- Collaborate with the research pharmacist to perform drug accountability, compliance and dosing
- Create and maintain study files including regulatory binders, source documentation and other materials
- Professional communication with sponsors, representatives and other study related parties
- Schedule and handle monitoring visits and/or trial audits, including but not limited to: coordinate with CRO/monitor, schedule time for the CRO/monitor to meet with PI, pharmacist, and other applicable staff, respond to data queries, document deviations with CRO and CIRB as applicable
- Participate in molecular tumor boards and/or regular physician meetings to review patient cases related to TIME Trials
- Other duties as assigned