What are the responsibilities and job description for the Clinical Research Coordinator (El Paso, TX) position at 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.
Department: Direct Clients
This is a full time position
