We are seeking an experienced and detail oriented Clinical Research Assistant (CRA) for our Cypress, TX and Houston, TX office. This is a full time position. The CRA 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.
- Completes paperwork related to subject visits.
- Pack & ship samples to laboratories.
- 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. Foreign Qualified Doctors encouraged to apply
- 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.
Job Type: Full-time
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Application Question(s):
- Are you a foreign medical graduate?
Education:
Experience:
- Clinical research: 1 year (Preferred)
Work Location: In person