Clinical Research Coordinator I — Start in Clinical Trials

UT Southwestern Medical Center; Dallas (TX); In loco; USD 45.000 - 62.000; Tempo pieno

Vantaggi offerti da questo lavoro

PPO medical plan

Paid Time Off

Retirement Programs

Parental Leave

Wellness programs

Tuition Reimbursement

Descrizione del lavoro

UT Southwestern Medical Center in Dallas is seeking a Research Coordinator to support clinical and basic research projects under the supervision of investigators. The role focuses on participant coordination, data quality, and regulatory compliance across studies.

Candidates should have a Bachelor's degree in medical or science field and at least one year of clinical research experience; CPR/BLS may be required depending on study protocols.

Competenze

• Bachelor's Degree or higher degree in medical or science related field.
• 1 year of clinical research experience.
• May consider additional years of experience or advanced degree in lieu of education or experience, respectively.

Mansioni

• Directly interacts with clinical research participants, as required, for the research study.
• Coordinate regulatory aspects of the trial including maintaining and developing regulatory information to comply with industry standards, University policies, FDA requirements or other hospital policies
• Coordinate and schedule study procedures as per protocol. Approved study protocols which have order sets built may be pended by the non-licensed coordinator with oversight by PI.
• Screen, recruit, enroll and follow subjects according to protocol guidelines. May also assist with the consent process
• Maintain and coordinate data collection information required for each study which may also include developing CRF's or data collection tools
• Assist in developing and implementing research studies to include writing clinical research protocols.

Formazione

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

Descrizione del lavoro

UT Southwestern Medical Center in Dallas is seeking a Research Coordinator to support clinical and basic research projects under the supervision of investigators. The role focuses on participant coordination, data quality, and regulatory compliance across studies.

Candidates should have a Bachelor's degree in medical or science field and at least one year of clinical research experience; CPR/BLS may be required depending on study protocols.