
Clinical Research Coordinator
1 week ago
We are seeking an experienced Clinical Trial Associate to join our team.
About the Role
This is a challenging and rewarding opportunity to work in a fast-paced environment, coordinating clinical trials from initiation to completion. You will be responsible for managing trial documents, communicating with site staff, and ensuring compliance with regulatory requirements.
Key Responsibilities
Document Management:
Oversee the preparation, review, and distribution of trial-related documents, including protocols, informed consent forms, and case report forms.
Site Communication:
Coordinate with site staff to ensure timely and accurate data collection, resolve issues, and maintain positive relationships.
Regulatory Compliance:
Verify that all trial activities adhere to Good Clinical Practice (GCP) guidelines and applicable regulations.
Collaboration:
Work closely with cross-functional teams, including research scientists, statisticians, and operational staff, to ensure seamless trial execution.
Requirements
Qualifications:
Bachelor's degree in a life science or related field; experience in clinical trials, preferably in a coordinating role.
Skills:
Excellent communication and organizational skills, proficiency in Microsoft Office, and ability to work in a team environment.
Benefits
Professional Growth:
Opportunities for professional development, training, and advancement within the company.
Work-Life Balance:
Flexible working hours and a supportive work environment to maintain a healthy balance between work and personal life.
Others
If you are a motivated and detail-oriented individual who is passionate about clinical research, we encourage you to apply. Please submit your resume and a cover letter outlining your experience and qualifications. We look forward to hearing from you
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