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Job summary
A healthcare organization in Miami is seeking a Clinical Research Coordinator to oversee daily operations of clinical trials. The ideal candidate will be responsible for managing study protocols, obtaining informed consent, and ensuring compliance with ethical guidelines. The candidate should possess strong organizational skills and strong clinical research experience. This is a full-time, on-site position offering the opportunity to contribute to advancements in medicine.
Qualifications
Proficiency in obtaining Informed Consent and ensuring participants' understanding.
Experience in implementing study protocols and conducting clinical trials.
Knowledge of regulatory and ethical considerations in clinical research.
Responsibilities
Oversee daily operations of clinical trials.
Manage study protocols and coordinate with investigators.
Ensure accurate documentation and compliance with guidelines.
Skills
Obtaining Informed Consent
Clinical Research Experience
Attention to detail
Excellent interpersonal skills
Organizational skills
Education
Bachelor's degree in healthcare, science, or a related field
Job description
A healthcare organization in Miami is seeking a Clinical Research Coordinator to oversee daily operations of clinical trials. The ideal candidate will be responsible for managing study protocols, obtaining informed consent, and ensuring compliance with ethical guidelines. The candidate should possess strong organizational skills and strong clinical research experience. This is a full-time, on-site position offering the opportunity to contribute to advancements in medicine.