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Clinical Trials Specialist
3 weeks ago
**About the Role:**
The Clinical Trials Specialist will play a crucial role in supporting our clinical research activities, focusing on site monitoring, data management, and collaboration with cross-functional teams. We are looking for a skilled professional with a passion for delivering exceptional results in a fast-paced environment.
Key Responsibilities:
- Conduct site monitoring visits, ensuring compliance with regulatory requirements and SOPs.
- Develop and maintain detailed project plans, schedules, and timelines, ensuring timely completion of tasks.
- Collaborate with data managers to ensure accurate and complete data collection and entry.
- Analyze and interpret data, identifying trends and areas for improvement.
- Communicate effectively with study team members, investigators, and other stakeholders to ensure seamless study execution.
Requirements:
- Bachelor's degree in a related field or equivalent experience.
- At least 2 years of clinical research experience, preferably in a related allied health profession.
- Excellent understanding of ICH GCP Guidelines and local regulatory requirements.
- Strong analytical and problem-solving skills, with the ability to communicate complex information effectively.