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Mount Sinai Health System · New York, NY

Clinical Research Assistant II - Tisch Cancer Center

TypeFull time
ScheduleDays
EducationHS diploma
PostedJun 29
✓You’ll need
Education
✓Associates Degree in related field or HS Diploma with equivalent related experience
Qualifications
2 years in research environment preferred
Excellent written and oral communication skills preferred
Exceptional attention to detail and accuracy preferred
Ability to juggle multiple tasks and schedules preferred
Mount Sinai Health System
Nonprofit · New York, NY · 5 hospitals
1,362open roles
Want the next healthcare job in New York by email?
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✓You’ll need
Education
✓Associates Degree in related field or HS Diploma with equivalent related experience
Qualifications
2 years in research environment preferred
Excellent written and oral communication skills preferred
Exceptional attention to detail and accuracy preferred
Ability to juggle multiple tasks and schedules preferred
Mount Sinai Health System
Nonprofit · New York, NY · 5 hospitals
1,362open roles
Want the next healthcare job in New York by email?
Weekly, free, unsubscribe with one click.

Full employer posting

The Clinical Research Assistant II performs a wide variety of activities related to clinical research study on behalf of the Tisch Cancer Center, Cancer Clinical Trials, Multiple Myeloma team. The Clinical Research Assistant II supports the Clinical Research Team and P. I. in their efforts to successfully complete study related activities, including data maintenance, and related documentation.

The Tisch Cancer Center (TCC) is a vital component of the Icahn School of Medicine at Mount Sinai Hospital and plays a key role in the Mount Sinai Health System, which is one of the largest health care systems in the nation. We are a National Cancer Institute (NCI)-designated center and provide a multidisciplinary approach to cancer treatments and clinical breakthroughs that may one day put an end to cancer. Responsibilities Provides organizational, administrative and clinical assistance for the Multiple Myeloma research study program such as preparing and coordinating meetings with various departments and personnel, assist in invoice and payment resolution Performs activities in accordance with established policies and procedures related to clinical research study protocols, including but not limited to: answering phone calls, scheduling appointments, coordinating specimen collection, assist with data entry, and review of safety reports. .

Collects and records study data. Inputs all information accurately into database. 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.

Collecting and processing specimens and point of care testing, preparing for exam, etc. Assists clinicians with various procedures, takes vital signs, relays instructions to patients and or families; answers calls and provides pertinent information. Performs other related duties.

Qualifications Associates Degree in related field or HS Diploma with equivalent related experience 2 years in research environment preferred Preferred: Excellent written and oral communication skills Exceptional attention to detail and accuracy Ability to juggle multiple tasks and schedules

Full time · Day shift

About the role

Provides organizational, administrative and clinical assistance for the Multiple Myeloma research study program such as preparing and coordinating meetings with various departments and personnel, assist in invoice and payment resolution