Clinical Research Coordinator
16 hours ago
We are seeking a highly skilled Clinical Research Monitor to join our team.
The selected candidate will be responsible for the coordination of ongoing clinical trials at assigned sites, ensuring timely and accurate completion of tasks.
Key Responsibilities:
- Schedule and conduct monitoring visits to clinical trial sites in accordance with study protocols and regulatory requirements.
- Assist senior team members in coordinating ongoing clinical trials.
- Undergo comprehensive training in monitoring processes and Good Clinical Practice (GCP).
- Provide training to site personnel on GCP guidelines and specific study-related activities.
Requirements:
- Strong organizational and communication skills.
- Ability to work independently and as part of a team.
- Good understanding of clinical trial processes and regulations.
Benefits:
- Opportunity to work in a dynamic and growing industry.
- Chance to develop skills and expertise in clinical research monitoring.
- Competitive compensation and benefits package.
We offer a supportive work environment and opportunities for professional growth. If you are a motivated and detail-oriented individual, we encourage you to apply for this exciting opportunity.
Keyword: ClinicalResearchMonitor
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