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Clinical Trials Research Asst/Data Management - Department of Surgery

University of Iowa · Posted Nov 7, 2026

Iowa City, Iowa, United States
On-site
Contract · Associate

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The clinical trial research assistant/ data manager will apply clinical skills to administer, deliver, and evaluate research protocols, including subject recruitment, protocol management, and data collection.

Responsibilities

Perform clinical/health care research activities.
Screen, recruit, enroll and obtain informed consent for clinical research activities.
Educate patient scope of study, potential risks and benefits, possible alternative, and study requirements.
Relay information to principal investigator and verify patient eligibility.
Oversee the recruitment of subjects and scheduling of trial-related procedures.

Skills

Clinical research activities Informed consent Protocol management Data collection Regulatory documentation IRB submissions CRF development

ACTM

ACTM

Responsibilities

Requirements

Skills

Benefits

Clinical Trials Research Asst/Data Management - Department of Surgery

Responsibilities

Skills

Benefits

CRF development jobs

Responsibilities

Requirements

Skills

Benefits

Responsibilities

Skills

Benefits