Description
Clinical Research Coordinators at the Depression and Anxiety Center for Discovery and Treatment (DAC) are responsible for research, clinical, and administrative tasks related to conducting a given study, including: running experimental procedures, entering and analyzing data, conducting phone screens on potential subjects, assisting with protocol development and modifications, as well as preparing presentations and publications.

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

Qualifications

• Bachelors degree in science or related field preferred or a combination of relevant research experience and education
• 0-2 years of research/human subjects experience
• Major, minor, or substantial coursework in Psychology, Neuroscience, Biology, Biochemistry, or other relevant field of study.

Employer Description

• 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 dutie