Clinical Research Coordinator at Sigma Consult

Role Summary:

As a Clinical Research Coordinator, you will play a crucial role in facilitating clinical trials by coordinating and managing various aspects of research projects to ensure compliance with protocols and regulations.

Responsibilities:

• Coordinate and manage all aspects of clinical research projects, including study initiation, monitoring, and close-out.
• Develop and maintain study documentation, including protocol, informed consent forms, and case report forms.
• Recruit and enroll study participants according to protocol criteria.
• Collect and record study data accurately and in compliance with regulatory requirements.
• Communicate regularly with study sponsors, investigators, and study team members.
• Ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory guidelines.

Requirements:

• Bachelor's degree in a relevant field (e.g., Nursing, Pharmacy, Life Sciences).
• Proven experience in clinical research coordination or a related role.
• Knowledge of clinical research regulations and guidelines.
• Strong organizational and time management skills.
• Excellent communication and interpersonal skills.
• Attention to detail and accuracy in data collection and documentation.

Benefits:

• Competitive salary package.
• Opportunities for professional development and career advancement.
• Access to cutting-edge research facilities and resources.
• Supportive work environment fostering collaboration and innovation.
• Comprehensive benefits package including health insurance and retirement benefits.