Clinical Research Coordinator A

Job Description Summary

Renal division in the department of medicine supports a diverse group of investigators, involving work on a wide spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated trials. This position is responsible for study coordination for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects within the Renal, Electrolyte, and Hypertension Division.

Job Responsibilities

• Screen, recruit and enroll consenting patients using Good Clinical Practice guidelines and conduct compliance monitoring of study participants.
• Conduct study related visits, including procedures such as blood draws, vitals, medical history, ECGs, processing and shipping of biological specimens and manage study data and regulatory files per GCP.
• Work with Regulatory Affairs Specialist to prepare for audits, review regulatory binders, perform internal audit and other QA activities.
• With supervision, assist in preparation of research protocols and documents.
• Manage/coordinate/organize the daily work of research assistants.

Qualifications

• Bachelor of Science and 1 to 2 years of experience or equivalent combination education and experience is required.
• Effective problem solving abilities; effective communication and writing skills; strong organizational and time management skills.