Full-Time

Clinical Research Program Coordinator

Updated on 3/14/2025

University of Texas - Austin

University of Texas - Austin

Compensation Overview

$48kAnnually

Mid

No H1B Sponsorship

Austin, TX, USA

Category
Public Health
Biology Lab & Research
Biology & Biotech
Required Skills
Word/Pages/Docs
Excel/Numbers/Sheets
Requirements
  • Bachelor's Degree and three (3) years of experience in clinical research or related field
  • Previous experience with subject recruitment and retention in clinical environments, and data management
  • Comfort with and interest in working in a clinical environment, including the operating room
  • Ability to communicate with peers, patients, and patient families in a clear, understandable and professional manner on the phone and in person
  • Ability to address individuals and information with a high degree of sensitivity and confidentiality in various delicate, formal, or urgent situations
  • Demonstrated use of good written and verbal communication skills
  • Effective project management skills, including the ability to plan, organize and schedule work in an efficient and productive manner, focusing on key priorities and meeting deadlines
  • Effective organizational skills and attention to detail
  • Proficient in Microsoft Word, Excel, and PowerPoint
  • Ability to maintain regular, reliable, and punctual attendance
  • Ability to learn and apply new information, be flexible
  • Obtaining external partners' site-specific clinical privileges, such as immunizations, is required
Responsibilities
  • Responsible for the day-to-day management and operations of multiple large-scale clinical research projects under the guidance of principal investigators from the Department of Surgery and Perioperative Care
  • Execute clinical research protocols including screening, recruitment, obtaining informed consent, completing study related procedures, accounting for study drug and investigational devices, and documenting compliance
  • Responsible for clinical tasks (examples include lab preparation of specimens, vital signs, ECGs) and administration of questionnaires
  • Manage logistics associated with clinic- and hospital-based clinical research for industry-sponsored projects
  • Manage data collection
  • Work with pre-and post-award contacts to coordinate contracting, invoicing and purchasing
  • Responsible for communications with sponsors, clinical research organizations (CROs), central and local IRBs, vendors, participants, and investigators
  • Assist faculty in developing research protocols and grant proposals, informed consent forms, questionnaires, recruitment tools and other forms of documentation
  • Maintain ethical approval for studies, from initial study approval through study amendments, annual continuations and terminations. Maintain all case report forms (CRF) and source documents according to FDA and IRB guidelines
  • Coordinate interdisciplinary teams of investigators, research assistants, clinical staff members and others contributing to executing elements of research being conducted within Dell Medical School and affiliates. Ensure that all investigators and staff executing research are appropriately trained in research human subjects research and procedures
  • Other related duties as assigned
Desired Qualifications
  • Master's degree in public health, healthcare administration or other related field and five (5) years of experience providing project management and support for large scale clinical research studies
  • At least 1 year of experience in healthcare and research in an academic setting
  • Fluency in Spanish
University of Texas - Austin

University of Texas - Austin

View

Company Size

N/A

Company Stage

N/A

Total Funding

N/A

Headquarters

N/A

Founded

N/A