- San Diego, California, United States
- On-site
- Full-time · Mid
- $89K–$118K per year
- 2+ years
A highly visible role responsible for managing the successful execution of ATRI clinical trials, supporting clinical research efforts across national and international sites.
Compensation
The annual base salary range for this position is $88,721.66 - $118,129.88.
Responsibilities
- Collaborate with the Project Director and other functional groups in the planning and administration of all phases of multi-site clinical trials
- Set and maintain priorities and timelines for project implementation, maintenance, and closeout of clinical trials across multiple national and international ATRI clinical trial study sites
- Conduct and drive study planning meetings including the management of meeting minutes, logging action items and decisions, and tracking action items to completion
- Serves as the primary point of contact and guidance expert for assigned studies
- Provides work direction and delegates tasks to other staff personnel
Requirements
- Bachelor's degree In Biological Science Or related field(s)
- Nice to have: Master's degree In Neurosciences Or Public Health Or Pharmacology
- Nice to have: Certified Clinical Research Associate (CCRA)
- Nice to have: Certified Clinical Research Coordinator (CCRC)
- Nice to have: data management
Skills
industry experience in pharmaceutical, biotechnology, clinical research organization and/or nursing settingmedical devicesmedical terminologyICH-GCP guidelinesFDA guidance documentstechnical documentationwritingdata organization in spreadsheets and databasesproject managementOmniPlanspreadsheetsdatabases