• Will work closely with the Principal Investigators (PIs), study staff and clinical staff.
• Responsibilities include but are not limited to screening patients to determine eligibility/verification of enrollments, facilitating study activities, coordinating/conducting informed consent discussions, assisting with consent issues, and monitoring patients for complications and outcomes.
• Conduct and is responsible for all study-related activities including screening & consent and enrollments, data collection/entry, and compliance with the regulatory process.
• Encouraged to prepare strategies to improve enrollment/retention. May need to maintain and order supplies as needed.
• Will Assess protocol feasibility and establish protocol-specific recruitment plans.
• May be required to train junior staff and oversee the work of others as directed.
• Will be required to communicate effectively with study participants and potential community recruits.
• Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols.
• Recruits research subjects and conducts interviews and research assessments.

• Minimum Education Requirement: Bachelor’s Degree
• Experience Requirement: At least 3-5 years of clinical trial/clinical research experience within industry/sponsor trials
• Education/Experience Substitution: A combination of relevant education and experience will be considered in place of the specified educational and/or experience requirements.
• Preferred Certification: CRC certification is preferred but not required.

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