What are the responsibilities and job description for the Clinical Research Assistant position at Headlands Research?
Overview
At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. We’re an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant outreach and participation. Founded in 2018, our company is in high growth mode; we operate 18 clinical trial sites in the US and Canada and have rapid expansion plans.
The Role
Pharmasite, a Headlands Research site is looking for a Clinical Research Assistant who is a Certified Medical Assistant to assist coordinators in conducting clinical research study visits.
Responsibilities
Assist clinical research coordinators in the conduct of clinical trials. Responsibilities include but are not limited to:
- Perform phlebotomy & vital checks (EKGs, etc.)
- Assist in preparation for study visits
- Assist in the collection of clinical data
- Enter data into EDC, CTMS
- Specimen processing
- Assist with ancillary scheduling
- Order study participant meals
- Process study participant stipends
Qualifications
- Certified Medical Assistant
- Experience interacting with patients
- Clinical research experience preferred
- Knowledge of medical terminology and laboratory skills preferred
- Knowledge of Microsoft Office required
- Excellent interpersonal and communication skills—interact effectively with patients, staff, sponsors, and others as required.
- High attention to detail
- Ability to set priorities and meet deadlines
- Ability to work as a member of a team