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:
Bachelor's (Preferred)
Experience:
Clinical research: 1 year (Preferred)
Work Location: In person
Numbers & Facts
Location
Cypress, TX
Skills
Clinical Assessmentunmatched
Clinical Practices/Protocolsunmatched
Clinical Researchunmatched
Clinical Trialunmatched
Communication Skillsunmatched
Computer Skillsunmatched
Data Entryunmatched
Detail Orientedunmatched
Informed Consentunmatched
Medical Terminologyunmatched
Order Picking/Packingunmatched
Organizational Skillsunmatched
Phlebotomyunmatched
Presentation/Verbal Skillsunmatched
Specimens/Samplesunmatched
Standard Operating Procedures (SOP)unmatched
Time Managementunmatched
Vision Planunmatched
Writing Skillsunmatched
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