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Clinical Research Associate / Clinical Ops Coordinator
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Job Description
- Req#: b9d20cc1-b539-4577-a271-a7f010ab336b
Employer Industry: Medical Device Development
Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Engage in meaningful work that empowers women to take control of their health
- Collaborative and dynamic startup environment
- Chance to make a direct impact on clinical trials and data integrity
- Work with innovative robotics, AI, and 3D ultrasound technologies
What to Expect (Job Responsibilities):
- Conduct site visits (initiation, monitoring, close-out) and ensure sites adhere to protocol and GCP
- Verify source data and promptly resolve queries
- Enter and review clinical data in EDC, ensuring accuracy and timeliness
- Support study start-up activities, including regulatory submissions and site set-up
- Maintain study files and trackers, and assist with vendor coordination as needed
What is Required (Qualifications):
- 2-4 years of experience in clinical research (CRA, coordinator, or clinical ops)
- Strong knowledge of GCP and basic regulatory requirements
- Proficiency with EDC, eTMF, and Excel/Google Sheets
- Excellent attention to detail and commitment to data quality
- Resourceful, adaptable, and able to thrive in a startup environment
How to Stand Out (Preferred Qualifications):
- Experience in oncology, imaging, or medical devices
- Prior exposure to risk-based monitoring
- Familiarity with dashboards, trackers, or clinical operations technology
#MedicalDevices #ClinicalResearch #StartupCulture #DataIntegrity #WomenHealth
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