Key Responsibilities:

• Recruit and screen patients for APOL1 study.
• Execute Informed Consent Forms according to ICH and GCP guidelines.
• Perform assessments at study visits according to protocol. Document study visits in source according to ALCOA-CCC.
• Perform phlebotomy, process, and ship blood and urine samples according to protocol.
• Enter source document data into respective EDC vendor system (Medidate RAVE, etc) and respond to queries in a timely manner.
• Perform vitals, ECG, and other study assessments required by protocol.
• Record adverse events and serious adverse events per sponsor guidance. Maintain timely follow-up to determine resolution of adverse event. Monitor, dispense, collect investigational product; maintain accountability logs and temperature logs and report temperature excursions; work in IRT systems.
• Schedule, prepare, and conduct visits (QV, SIV, IMVs, COV) with sponsor/CRO team.

Schedule

• Part Time: 20 hours a week depending on patient needs
• Remote work when not needed for Patient visits

Requirements:

• Minimum 1 year of CRC experience, experience in nephrology prefered,
• SoCRA or ACRP Certified