What are the responsibilities and job description for the Clinical Research Assistant position at Tekton Research Inc?
The Research Assistant supports the research team in daily operations of clinical trials. It is the responsibility of the Research Assistant to communicate with study team and, site manager and study participants regarding necessary information of the study. Adherence to site SOPs is required.
Please Note: This is a fully on-site position and does not offer remote or hybrid work:
Reports to: Site Manager/Director
Job Description:
- Support the recruitment efforts through pre-screening and scheduling patients
- Prepare source binders for patient visits
- Medical record requests
- Ensure e-diaries are scheduled and completed by subject
- Check patients in/out
- Ensure patients are paid
- Answer and transfer phone calls
- Inventory lab and study supplies
- Record adverse event and side effect data and confer with investigators regarding the reporting of events to sponsors
- Resolve all auto queries and enter data in the EDC within 24 hours of query being issued by sponsor
- Maintain accurate master logs for each study. (ICF, patient ID, and enrollment)
- Maintain accurate temperature logs daily as needed
- Phlebotomy / Blood draw and processing as needed
- EKGs
- Vitals
- Other duties as assigned
Required Skills/Abilities:
- 6 months Medical Assistant/EMT or other medical experience preferred
- Ability to work independently and as a member of a team
- Research experience is a plus
Education and Experience:
- GED or HS Diploma required (Some College preferred)