SCTx Clinical Research Associate I or II
About The Position
The Clinical Research Associate I or II assists with organizing, implementing, and completing clinical research studies in compliance with applicable laws and regulations, institutional and departmental guidelines, Good Clinical Practice (GCP) standards, and budget requirements. The role creates or drafts, collects, and reviews study-related documents; tracks study progress and completion of activities; and performs in-house and on-site data monitoring. For the Associate II level, responsibilities also include developing and managing systems and procedures for tracking study progress, assessing, initiating, managing, monitoring, and closing clinical sites, and monitoring multiple studies. The Associate I role focuses on immunotherapy clinical research studies. This is a limited-term position estimated to last 12 months, with the possibility of extension, and requires travel outside Washington state.
Requirements
- Clinical Research Associate I: Bachelor’s degree and at least one year of related experience in clinical trials.
- Clinical Research Associate II: Bachelor’s degree in a biological science or health-related field, or equivalent job experience.
- Clinical Research Associate II: At least two years of related experience, including at least one year as a clinical research associate.
- Clinical Research Associate II: Experience monitoring and managing multiple studies.
- Clinical Research Associate II: Experience reviewing clinical trial materials and reports.
Nice To Haves
- Clinical Research Associate certification.
- Clinical Research Associate I: Experience as a Clinical Research Associate (CRA) or Clinical Research Coordinator (CRC).
- Clinical Research Associate I: Familiarity with MS Word, Excel, PowerPoint, and electronic data capture (EDC) software.
- Clinical Research Associate I: Experience with immunotherapy research.
Responsibilities
- Assist in organizing, implementing, and completing clinical research studies in compliance with applicable laws and regulations, institutional and departmental guidelines, Good Clinical Practice standards, and budget requirements.
- Create or draft, collect, and review study-related documents.
- Track study progress and completion of study activities.
- For the Clinical Research Associate II role, develop and manage systems and procedures for tracking study progress and completion of study activities.
- For the Clinical Research Associate II role, assess, initiate, manage, monitor, and close clinical sites.
- Perform in-house and on-site data monitoring, including monitoring visits.
- Travel outside Washington state.
Benefits
- Medical, dental, and vision plans.
- 403(b).
- Life insurance.
- Paid time off.
- Tuition reimbursement.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
