
Senior Clinical Operations Specialist
2 days ago
Job Overview
- This role is responsible for ensuring the highest standards of care and safety in research subject safeguarding, with a focus on clinical trial operations.
Key Responsibilities:
- Safeguarding the wellbeing of research subjects by conducting procedures with the highest standards of care and safety.
- Reviewing study protocols to ensure alignment with regulatory, health, and safety standards.
- Recruiting and coordinating communication with clinical trial volunteers and patients.
- FOLLOWING APPLICABLE REGULATIONS GLOBALLY AND BY REGION.
- Collaborating with cross-functional teams to develop study materials.
- Monitoring trial progress and addressing any issues that arise during the study.
- Providing organizational related support or service.
Requirements:
- High school diploma or equivalent required.
- Associate's degree or higher in a related field preferred.
- Minimum of 2 years of experience in clinical operations or a related field.
- Strong understanding of clinical research protocols and regulatory requirements.
Benefits:
- Opportunity to work on diverse clinical trials projects.
- Collaborative work environment.
- Professional growth and development opportunities.
Get to know us:
- Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA.
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