Entry-Level Clinical Research Coordinator

Mount Sinai Morningside; New York (NY); Vor Ort; USD 59.000 - 74.000; Vollzeit

Zusammenfassung

Mount Sinai Morningside is seeking a Clinical Research Coordinator to support daily activities of clinical research studies, obtain informed consent, and maintain study data. You will assist in preparing grant applications and IRB/GCO submissions, and ensure proper documentation and data integrity throughout the trial lifecycle.

The role involves coordinating study activities, communicating with participants, and supporting regulatory filings.

Qualifikationen

• Bachelor's or Master's degree in Science or related field.
• No experience required; 1 year of research experience preferred.

Aufgaben

• Collects and records study data and inputs information into the database.
• Obtains informed consent and educates participants on study requirements.
• Assists in coordinating activities for clinical research studies including screening and registration of subjects.
• Prepares grant applications and IRB/GCO submissions.
• Maintains source documents and subject files per hospital procedures and compiles data from chart reviews.
• S ecures, ships and delivers clinical specimens and prepares for monitoring visits.

Kenntnisse

Data entry

Informed consent

Study coordination

Communication

Ausbildung

Bachelor's or Master's degree in Science

Jobbeschreibung

Mount Sinai Morningside is seeking a Clinical Research Coordinator to support daily activities of clinical research studies, obtain informed consent, and maintain study data. You will assist in preparing grant applications and IRB/GCO submissions, and ensure proper documentation and data integrity throughout the trial lifecycle.

The role involves coordinating study activities, communicating with participants, and supporting regulatory filings.