Clinical Research Coordinator - CEDENT

Role Summary
We are looking for a Clinical Research Coordinator to join our team. This full-time, on-site role involves managing informed consent processes, ensuring protocol adherence, conducting research, and facilitating clinical trials in alignment with organizational values and mission.
 

Responsibilities

• Oversee informed consent processes and ensure compliance with ethical standards.
• Monitor and enforce protocol adherence across clinical trials.
• Conduct high-quality research and maintain the integrity of data collection and reporting.
• Coordinate and facilitate clinical trials to meet organizational and regulatory standards.
• Collaborate with multidisciplinary teams to achieve research objectives.

Requirements

• Proficiency in informed consent and protocol management.
• Proven experience in clinical research and clinical trials.
• Strong research aptitude with the ability to deliver accurate, timely data.
• Exceptional organizational and communication skills.
• Keen attention to detail and ability to collaborate effectively within a team.
• Bachelor’s degree in Nursing, Biology, Health Sciences, or a related field.
• Certification in Clinical Research is preferred but not required.