Clinical Research Coordinator

We are seeking an experienced and detail oriented Clinical Research Coordinator (CRC) for our Cypress, TX office. This is a full time position. The CRC will work under the supervision of the Principal Investigator(s) and Site research manager and will include all study related activities during the clinical research timeline from pre-site visit (PSV) through study close-out. Duties include, but are not limited to:
• Recruits patients for clinical research studies based on study inclusion/exclusion.
• Obtains informed consent from subject and conducts the screening visit.
• Enrollment and follow up of eligible subjects according to protocol requirements.* Coordinate and conduct subject visits.
• Assure all procedures are conducted in compliance with the clinical protocol and standard operating procedures (SOPs)
• Work closely with Principal Investigators (PIs) to assure subjects receive appropriate medical evaluation and care.
• Attend sponsor investigator meetings as needed for assigned clinical trials.* Perform blood draws and taking patient vital signs.
• Completion of study documents, including electronic data entry.
• Communicate professionally and timely with all relevant staff involved in the clinical research study.
• Other duties as assigned.
Qualifications:
• Bachelors degree preferred.
• Phlebotomy and ECG experience( Preferred)
• Previous experience as a Clinical Research Coordinator.
• Excellent verbal and written communication skills, including medical terminology.
• Professional, self starter and well organized.
• Attention to detail.
• Strong computer skills.