Clinical Research Associate (CRA) I

Responsibilities:

• Review protocols and comply with study-specific activities.
• Communicates in an appropriate and professional manner with study subjects and unit personnel.
• Maintain accurate and complete source data.
• Perform study protocol related activities, i.e. phlebotomy, sample processing, ECG collection, vital signs, height/weight, etc., as assigned.
• Maintain safety and confidentiality of study subjects throughout the study.
• Understands and complies with SOPs, FDA regulations, and basic GCP requirements.

Requirements:

• High School Diploma or equivalent.
• Clinical Medical Assistant, EMT, Paramedic, military medic with recent clinical experience, or higher.
• 1-2 years of work experience in a clinical or research environment, or in a patient care setting.
• 1-2 years of work experience in a role with phlebotomy responsibilities.

Note:

• Open 24/7, will work 8-hour shifts. There is no guarantee of hours. Some weeks may have no shifts whereas others may have 4 or 5. Shift options: day shift for training, then AM/PM and weekend availability for contract. Schedule comes out every 2 weeks.
• Name of Functional Area/Department: Clinical Pharmacology & Pharmacometrics Research Unit.

Top Skills:

• Phlebotomy.
• Lab work.
• ECG collection.
• Vital signs collection.
• clinical and/or hospital experience.