• Participate in recruitment activities to meet enrollment goals.
• Review medical history to Pre-Screen/Screen/Enroll study participants into clinical trials.
• Interact with potential study participants to introduce the study and perform the informed consent process.
• Coordinate, schedule and manage study visits.
• Conduct study procedures such as blood draws, ECGs, and vital signs.
• Collect study data and enter it into an electronic data capture system and maintain paper records.
• Creating data collection documents as needed.
• Collect study specimens such as blood, urine, etc., process, and ship to designated laboratories.
• Maintaining study supply inventory and equipment.
• Communication between study team and sponsors and vendors.
• Participate in sponsors monitoring visits.
• Maintain participant study binders.
• Assist to maintain regulatory documents.

Knowledge, Skills and Abilities:

• Ability to communicate effectively with different individuals/groups.
• Attention to detail.