Clinical Res Coordinator Hlth Job Description Template
Our company is looking for a Clinical Res Coordinator Hlth to join our team.
Responsibilities:
- Collects and manages patient and laboratory data for clinical research projects;
- Tracks and abstracts patient clinical and research information from various sources;
- Writes, edits, and renews IRB applications for various clinical trials;
- Analyze, compare and evaluate various courses of action for clinical research studies;
- Works with Cardiac Surgery faculty to assess and apply for new clinical trials;
- Attend biweekly or monthly research meetings to monitor for patients on-study safety and accrual trials;
- Meet data submission timeline expectations, and respond to data queries from the NCTN Cooperative Group statistical center in a prompt fashion;
- Assure that NCTN Cooperative Group clinical trials are conducted in compliance with GOP and ICH guidelines;
- Work closely with physicians, physician extenders, research nurses and pharmacists for the study startup and maintenance;
- Work with research nurses to assure that the study calendar is followed with regards to study visits and form completion;
- Screen all adverse events for seriousness and review adverse reports and report events to the IRB as well as the NCTN Cooperative Group.
Requirements:
- Accept direction and function both independently and collaboratively with staff at all levels within the setting;
- Bachelor’s degree in a health-related field;
- Prior experience in working as a research coordinator or similar role;
- Advanced written and verbal communication skills;
- SOCRA or ACRP certification;
- Master’s Degree;
- Must understand issues with regards to human subjects research;
- Basic computer skills are required and experience in extracting information from electronic medical records would be useful;
- Bachelor’s Degree in a health science discipline or equivalent combination of education and experience required;
- Previous experience with Epic, MiChart, Oncology research;
- Three to five years’ previous experience in the conduct of clinical research including IRB applications.