Data Coordinator I - Tisch Cancer Institute

Mount Sinai Health System • New York, NY

6d

About The Position

A Data Coordinator I position is currently available within the Multiple Myeloma (MM) research team at the Tisch Cancer Institute. The Data Coordinator reviews, extracts, cleans and audits data from various source documents so that the appropriate data can be shared. He/she also ensures the accuracy of the data and acts as a resource to all users of the database. The Tisch Cancer Institute 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. The Data Coordinator I, reviews, cleans and audits the data so that the appropriate data can be shared. The Data Coordinator extracts data and generates basic and moderately complex reports as required. The Data Coordinator ensures the accuracy of the data and acts as a resource to all users of the database.

Requirements

• Bachelors degree or equivalent education and experience
• No experience required.
• Excellent written and oral communication skills
• Exceptional attention to detail and accuracy
• Ability to juggle multiple tasks and schedules.

Nice To Haves

• One year of database application management experience preferred
• Oncology knowledge desirable

Responsibilities

• Collects and records study data from various source documents into different case report systems.
• Inputs all information accurately into database
• Maintains source documents and subject files in accordance with hospital procedures.
• Reviews and audits database on a regular basis to ensure accuracy of data.
• Makes corrections and additions to database records as required.
• Ensures accurate and complete compilation of subject data through chart reviews.
• Assist with recording and logging of safety reports for weekly reviews.
• Updates and resolve queries or issues within the databases in a timely manner.
• 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, etc.
• Performs other duties as required.

What This Job Offers

• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees