Clinical Research Coordinator I

Position Summary: Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO).

Essential Functions and Responsibilities:

1. Assure all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines.
2. Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs. 
3. Respond to queries in a timely fashion.
4. Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.
5. Assist multidisciplinary team in research activities. 
6. Maintain study binders and filing according to protocol requirements and CTO policy.
7. Adhere to all KCI & CTO policies and procedures.

Qualifications:

Required:

1. Bachelor’s degree required or equivalent combination of education and experience.
2. Medical and/or science experience/education preferred.
3. Proficient with the Microsoft suite including Excel and Power point.
4. Demonstrated attention to detail.

Preferred: 

1. Medical and/or science experience/education preferred.

Knowledge, Skills, and Abilities:

1. Initiative and ability to work independently.
2. Ability to analyze problems and effect resolution.
3. Ability to maintain cooperative working relationships with internal and external units in a clinical research environment.
4. Ability to provide excellent customer service.
5. Ability to follow instruction and follow tasks through completion.