Vanderbilt University Medical Center
Clinical Trials Associate I
Vanderbilt University Medical Center, Nashville, Tennessee, United States, 37247
Discover Vanderbilt University Medical Center
Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, VUMC is a community of individuals who come to work each day with the simple aim of changing the world.
It is a place where your expertise will be valued, your knowledge expanded, and your abilities challenged.
Vanderbilt Health is committed to an environment where everyone has the chance to thrive and where your uniqueness is sought and celebrated.
It is a place where employees know they are part of something that is bigger than themselves, take exceptional pride in their work and never settle for what was good enough yesterday.
Vanderbilt’s mission is to advance health and wellness through preeminent programs in patient care, education, and research. Organization
Pediatric Infectious Disease Job Summary
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. Key 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. Research Data Collection
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. Maintaining Records
Ensures complete source documentation in record. Meets with and assists in response to sponsors and monitors to ensure compliance with protocol and applicable regulations. Examine data and records to ensure compliance with protocol. Position Qualifications
Relevant Work Experience – Less than 1 year Education – Associate's Vanderbilt Health is committed to fostering an environment where everyone has the chance to thrive and is committed to the principles of equal opportunity. EOE/Vets/Disabled.
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Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, VUMC is a community of individuals who come to work each day with the simple aim of changing the world.
It is a place where your expertise will be valued, your knowledge expanded, and your abilities challenged.
Vanderbilt Health is committed to an environment where everyone has the chance to thrive and where your uniqueness is sought and celebrated.
It is a place where employees know they are part of something that is bigger than themselves, take exceptional pride in their work and never settle for what was good enough yesterday.
Vanderbilt’s mission is to advance health and wellness through preeminent programs in patient care, education, and research. Organization
Pediatric Infectious Disease Job Summary
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. Key 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. Research Data Collection
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. Maintaining Records
Ensures complete source documentation in record. Meets with and assists in response to sponsors and monitors to ensure compliance with protocol and applicable regulations. Examine data and records to ensure compliance with protocol. Position Qualifications
Relevant Work Experience – Less than 1 year Education – Associate's Vanderbilt Health is committed to fostering an environment where everyone has the chance to thrive and is committed to the principles of equal opportunity. EOE/Vets/Disabled.
#J-18808-Ljbffr