Dermatology Clinical Research Coordinator - Entry Level

Mount Sinai; United States; On-site; USD 23,000 - 57,000; Full time

Job summary

The Mount Sinai Dermatology Department is seeking a Clinical Research Coordinator to conduct and assist in clinical studies under supervision, obtain informed consent, screen participants, enroll patients, and coordinate study activities with investigators and clinical staff.

You will collect, organize and analyze data, assist with grant applications and regulatory submissions, maintain source documents, ship specimens when required, support site visits, and help ensure data quality,

Qualifications

• Bachelor’s degree in science or related field preferred or a combination of relevant research experience and education.
• 0-2 years of research/human subjects experience.

Responsibilities

• Conducts routine and standardized human subjects research under direct supervision of the Principal Investigator or senior clinical research staff.
• Assists in obtaining informed consent, screening participants for eligibility, registering patients with sponsoring agencies, administering questionnaires and answering telephone calls.
• Assists in the collection, analysis and review of experimental data for publication and presentation.
• Maintains source documents and subject files in accordance with Mount Sinai policies and procedures, ensuring accurate, confidential and complete data compilation.
• May secure and ship clinical specimens as required by the protocol.
• May assist in the preparation for regulatory agency site visits.
• Performs other related duties

Skills

Informed consent

Data collection

Participant screening

Education

Bachelor’s in science

Job description

The Mount Sinai Dermatology Department is seeking a Clinical Research Coordinator to conduct and assist in clinical studies under supervision, obtain informed consent, screen participants, enroll patients, and coordinate study activities with investigators and clinical staff.

You will collect, organize and analyze data, assist with grant applications and regulatory submissions, maintain source documents, ship specimens when required, support site visits, and help ensure data quality,