Clinical Trials Associate I

Vanderbilt University Medical Center • Nashville, TN

2d

About The Position

This position is with the VISPR Program, formerly called the Halasa/Chappell Lab, jointly led by Drs Natasha Halasa and Jim Chappell, within the Division of Pediatric Infectious Diseases at Vanderbilt University Medical Center. Our laboratory research concentrates on the etiology, epidemiology, prevention, and pathobiology of infectious diseases. This position performs a variety of duties involved in the collection, interpretation, and documentation of data in support of clinical trials with regular guidance. Assists in ensuring adherence to protocols, appropriate regulations, and deadlines.

Requirements

• Knowledgeable of protocols in order to determine specific criteria for eligibility or exclusion.
• Abstracts and records all patient data essential to the study onto required case report forms.
• Inputs all pertinent patient data into database accurately.
• Collects and monitors all study patients records to document treatments and outcomes as required by the protocol.
• Reports all adverse reactions according to VUMC and protocol guidelines.
• Calls or sends questionnaires to patient to check outcomes, survival rate, and quality of life.
• Examine data and records to ensure compliance with protocol.
• Associate's

Responsibilities

• Preparation and Coordination Knowledgeable of protocols in order to determine specific criteria for eligibility or exclusion.
• Sets up timeline of tests and required procedures.
• Prepares kits for procedures and labels tubes with specific times and dates for collection.
• Assists with monitoring compliance with protocol and regulations.
• Informs nurse of tests and procedures as needed.
• Conducts follow-up of study patients.
• Ensures deadlines are met for study
• Abstracts and records all patient data essential to the study onto required case report forms.
• Inputs all pertinent patient data into database accurately.
• Collects and monitors all study patients records to document treatments and outcomes as required by the protocol.
• Reports all adverse reactions according to VUMC and protocol guidelines.
• Calls or sends questionnaires to patient to check outcomes, survival rate, and quality of life.
• Ensures complete source documentation in record.
• Meets with and assists in response to sponsors and monitors to ensure compliance with protocol.
• Examine data and records to ensure compliance with protocol.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree
• Number of Employees: 5,001-10,000 employees