Entry-Level Clinical Research Coordinator: Make Impact

Mount Sinai Morningside; New York (NY); On-site; USD 23,000 - 56,000; Full time

Job summary

The Clinical Research Coordinator at Mount Sinai Morningside is an entry-level human subjects researcher responsible for conducting and assisting in clinical studies under supervision of the PI or senior clinical research staff. This role involves obtaining informed consent, collecting and organizing study data, and supporting regulatory submissions.

You will work under supervision, assist with grant applications and regulatory documents, and help ensure compliance with Mount Sinai policies

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 using appropriate research or interview techniques specific to subject matter of the research project, under direct supervision of the Principal Investigator or senior clinical research staff.
• Assists in the activities related to clinical research including, but not limited to: 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. Ensures accurate, confidential and complete compilation of data.
• 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.

Education

Bachelor's degree in science or related field

Job description

The Clinical Research Coordinator at Mount Sinai Morningside is an entry-level human subjects researcher responsible for conducting and assisting in clinical studies under supervision of the PI or senior clinical research staff. This role involves obtaining informed consent, collecting and organizing study data, and supporting regulatory submissions.

You will work under supervision, assist with grant applications and regulatory documents, and help ensure compliance with Mount Sinai policies