What are the responsibilities and job description for the Clinical Research Coordinator (CRC) I position at Pharmaron CPC?
We are seeking a full-time Clinical Research Coordinator to join our Baltimore, MD Research team!
As a Clinical Research Coordinator, you will be responsible for coordination of all aspects of assigned clinical trials from pre-study planning through successful completion of all patient/subject visits and study documentation; directly involved in patient/subject care and study subject’s procedures and activities.
- Maintains detailed knowledge and understanding of assigned protocols, including all protocol requirements for patient/subject visits, obtaining informed consent, visit schedules, tests, procedures, laboratory information, and drug accountability requirements
- Responsible for all study documentation forms
- Coordinates and conducts patient/subjects’ visit schedules
- Assures that research participants receive appropriate medical evaluation and care
- Works with data management group to transcribe source data into eCRFs
- Facilitates sponsor monitoring and database clean-up process
- Attends sponsor Investigator/Study Coordinator meetings
- Conducts clinical research in compliance with all applicable regulations, including GCPs and company SOPs
Qualifications:
- Associate or Bachelor’s degree in related field
- 1-2 years of clinical trials/research experience is required