Clinical Research Coordinator I (PRN) – Patient & Data

University of Texas Southwestern Medical Center; Dallas (TX); In loco; USD 45.000 - 65.000; Part-time

Vantaggi offerti da questo lavoro

PPO medical plan

Paid Time Off

Retirement Programs (TRS)

Paid Parental Leave

Descrizione del lavoro

UT Southwestern Medical Center in Dallas seeks a Clinical Research Coordinator I PRN to coordinate research projects and manage patient participation. You will ensure data quality and assist in multiple drug, device, or biorepository studies across pulmonology and related fields, with on-call coverage as needed.

The role involves developing data collection tools, coordinating study visits, and supporting budgeting and regulatory tasks under PI oversight.

Competenze

• Bachelor's degree or higher in medical or science related field is required.
• 1 year of clinical research experience is required.
• CPR/CPRAED or ACRP/SOCRA certification is a plus.

Mansioni

• Interact with clinical research participants via telephone, telehealth, or in-person.
• Coordinate regulatory aspects of the trial to comply with industry standards and policies.
• Schedule study procedures and manage protocol compliance.
• Screen, recruit, enroll and follow subjects per protocol.
• Develop and maintain data collection tools and CRFs.
• Maintain and document subject-level data and study budgets.

Conoscenze

Clinical research experience

Regulatory knowledge

Communication skills

Computer skills

Formazione

Bachelor's Degree or higher in medical or science related field

Strumenti

Electronic Medical Records (EMR)

Clinical Trial Management System

Descrizione del lavoro

UT Southwestern Medical Center in Dallas seeks a Clinical Research Coordinator I PRN to coordinate research projects and manage patient participation. You will ensure data quality and assist in multiple drug, device, or biorepository studies across pulmonology and related fields, with on-call coverage as needed.

The role involves developing data collection tools, coordinating study visits, and supporting budgeting and regulatory tasks under PI oversight.