The Clinical Research Coordinator-II at the Depression and Anxiety Center for Discovery and Treatment will act as a clinical rater and will be responsible for the coordination and administration of clinical assessments of study subjects, particularly the SCID-5 for research. The candidate will also be responsible for preparing regulatory documents and assists in protocol submissions (e.g., for the Institutional Review Board, Grants and Contracts Office). The candidate may also be involved in analyzing and interpreting moderately complex clinical research data.

Essential Duties and Responsibilities
1. Assists in interpreting clinical research data via the SCID-5 and other measures.
2. Coordinates the clinical assessments of the study subjects, including but not limited to screening and evaluation of the study subjects.
3. Ensures accurate and complete compilation of subject data.
4. Prepares and ensures IRB and other regulatory documents are submitted.
5. Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.
6. Obtains informed consent under supervision of the Principal Investigator or Research Manager for studies enrolling vulnerable subjects and for studies involving genetic tests.
7. May independently obtain informed consent for other clinical studies.
8. May analyze moderately complex clinical research data.
9. Performs other related duties.

Under minimal supervision, coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists in protocol submissions (for e.g., Institutional Review Board, Grants and Contracts Office).

Duties and Responsibilities:
1. Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
2. Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
3. Prepares and ensures grant applications, IRB/GCO documents are submitted.
4. Ensures accurate and complete compilation of subject data through chart reviews.
5. Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of on going clinical trials.
6. Obtains informed consent under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies involving genetic tests.
7. Independently obtains informed consent for other clinical studies.
8. Mentors Clinical Research Coordinators in training.
9. Performs other related duties.

Strength Through Diversity

The Mount Sinai Health System believes that diversity is a driver for excellence. We share a common devotion to delivering exceptional patient care. Yet we’re as diverse as the city we call home- culturally, ethically, in outlook and lifestyle. When you join us, you become a part of Mount Sinai’s unrivaled record of achievement, education and advancement as we revolutionize medicine together.

We work hard to acquire and retain the best people, and to create a welcoming, nurturing work environment where you can develop professionally. We share the belief that all employees, regardless of job title or expertise, can make an impact on quality patient care.

Explore more about this opportunity and how you can help us write a new chapter in our story!

Who We Are

Over 38,000 employees strong, the mission of the Mount Sinai Health System is to provide compassionate patient care with seamless coordination and to advance medicine through unrivaled education, research, and outreach in the many diverse communities we serve.

Formed in September 2013, The Mount Sinai Health System combines the excellence of the Icahn School of Medicine at Mount Sinai with seven premier hospital campuses, including Mount Sinai Beth Israel, Mount Sinai Beth Israel Brooklyn, The Mount Sinai Hospital, Mount Sinai Queens, Mount Sinai West (formerly Mount Sinai Roosevelt), Mount Sinai St. Luke’s, and New York Eye and Ear Infirmary of Mount Sinai.

The Mount Sinai Health System is an equal opportunity employer. We comply with applicable Federal civil rights laws and does not discriminate, exclude, or treat people differently on the basis of race, color, national origin, age, religion, disability, sex, sexual orientation, gender identity, or gender expression.

EOE Minorities/Women/Disabled/Veterans