Cardiovascular Clinical Research Coordinator I

Mount Sinai Health System; United States; Presencial; USD 42 000 - 64 000; Tempo integral

Resumo da oferta

Mount Sinai Health System is seeking a Clinical Research Coordinator to support daily activities of clinical research studies, including consent, data collection, and regulatory documentation.

The role involves assisting with participant screening, subject registration, questionnaire administration, and preparation of IRB submissions. No mandatory experience is required, with one year of research preferred. Strong organizational skills are essential.

Qualificações

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

Responsabilidades

• Assists in the daily activities of clinical research studies; collects, maintains and organizes study information.
• Collects and records study data. Inputs all information into database.
• Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
• Assists in activities related to clinical research studies: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
• Assists in preparing grant applications, IRB/GCO for submission and filings.
• Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.
• Secures, delivers and ships clinical specimens as required by the protocol.
• Prepares for monitoring visits.
• Performs other related duties.

Conhecimentos

Informed consent

Data collection

Study coordination

Regulatory documentation

Formação académica

Science degree

Descrição da oferta de emprego

Mount Sinai Health System is seeking a Clinical Research Coordinator to support daily activities of clinical research studies, including consent, data collection, and regulatory documentation.

The role involves assisting with participant screening, subject registration, questionnaire administration, and preparation of IRB submissions. No mandatory experience is required, with one year of research preferred. Strong organizational skills are essential.