Chief Clinical Trial Specialist

Clinical Research Coordinator Job Description We are seeking a skilled Clinical Research Coordinator to lead the daily activities and administration of our clinical trials. Key Responsibilities: Coordinates with Principal Investigators, departments, and administration to ensure compliance with federal regulations and university policies. Collaborates with institutions to respond to audit findings and implement recommendations. Performs study feasibility assessments as requested. Prepares IRB and regulatory submission documents according to protocol requirements. Establishes and organizes study files, including regulatory binders, source documentation, and other materials. Provides effective communication of study requirements to team members, provides training, and documents training logs. Screens subjects for eligibility using protocol-specific inclusion and exclusion criteria. Required Skills and Qualifications: Bachelor's degree in Health or Life Science (Medicine, Biotechnology, Chemistry). At least 3 years of work experience in Clinical Research. Strong relationships with research stakeholders. Excellent communication, presentation, and interpersonal skills. Advanced English written and conversational skills. Knowledge of Good Clinical Practices Guidelines and international research guidelines. Benefits: This role offers opportunities for professional growth and development in a dynamic environment. How to Apply: Please submit your resume when applying. Thank you.

Creado: Jue, 01 de Ene de 1970