Job Details
Responsible for all data management aspects of clinical studies and efficiently performs all
data management activities within an assigned study or studies.
Provides data management expertise to the team in identifying opportunities for
improvement.
Ensures validity of research results through timely, accurate, and complete data submission,
query resolution, and reporting of deviations.
Demonstrates proficiency in the use of clinical and research-related computer programs.
Schedule, prepare and participate in all pharmaceutical site visits.
Assist Research Nurse(s) and appropriate departmental, and laboratory staff in collection,
storage, and shipment of patient specimens, radiology scans, reports, etc.
Ensures that relevant data from the source document are abstracted and recorded in the
clinical trial case report forms and that every data point can be verified within the source
document.
Utilizes analytical thinking, attention to detail, and problem-solving skills.Performs other
related work as needed.
Prepares for or participates in quality assurance audits conducted by study sponsors, federal
agencies, or specially designated review groups.
Participates in study-related documentation, such as protocol worksheets, procedural
manuals, adverse event reports, institutional review board documents, or progress reports.