Clinical Research Coordinator I
Position Summary: Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO).
Essential Functions and Responsibilities:
- Assure all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines.
- Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs.
- Respond to queries in a timely fashion.
- Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.
- Assist multidisciplinary team in research activities.
- Maintain study binders and filing according to protocol requirements and CTO policy.
- Adhere to all KCI & CTO policies and procedures.
Qualifications:
Required:
- Bachelor’s degree required or equivalent combination of education and experience.
- Medical and/or science experience/education preferred.
- Proficient with the Microsoft suite including Excel and Power point.
- Demonstrated attention to detail.
Preferred:
- Medical and/or science experience/education preferred.
Knowledge, Skills, and Abilities:
- Initiative and ability to work independently.
- Ability to analyze problems and effect resolution.
- Ability to maintain cooperative working relationships with internal and external units in a clinical research environment.
- Ability to provide excellent customer service.
- Ability to follow instruction and follow tasks through completion.