Role Summary
The role described is to serve as an integral member of the site and study team during study processes, including pre-admit, admission, orientation, conduct, discharge and study close.
Responsibilities
- Performs conduct procedures in strict compliance to the study protocol, Good Clinical Practice standards, Standard Operating Procedures (SOPs), QA/QC procedures, OSHA guidelines and other state and local regulations as applicable
- Provides assistance in the execution of clinical trials
- Ensures the well-being and safety of study participants
- Provides administrative and operational support
Education
- A high school diploma or G.E.D. and advanced medical procedure training or Phlebotomist certification is required.
Qualifications
- Minimum of one to two (1-2) years of experience in a clinical environment
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
- Able to obtain vital signs and perform ECGs
- Able to perform telemetry and insertion of intravenous catheters, or a willingness to learn
- Excellent oral, written and interpersonal communication skills
- Able to work independently and handle multiple competing priorities
- Able to work with tight deadlines
- Able to function independently within a team environment
- Excellent organizational and time-management skills and a strong attention to detail
- Proficient in MS Office Suite (Word, Excel, Outlook)
Skills
- Vital signs and ECG administration
- Telemetry and IV catheter insertion (or willingness to learn)
- Strong communication and teamwork abilities
- Independent and multi-tasking capabilities
- Strong organization and attention to detail
- Proficiency with MS Office Suite