What are the responsibilities and job description for the Clinical Research Coordinator III position at System One?
Job Title: Clinical Research Coordinator III
Location: Pittsburgh, PA, Hybrid: Combination of On-Campus or Remote determined by the department.
Schedule: Varied based on participants schedule
Type: Direct Hire or 6 -12 month Contract based on department needs
Overview:
A top-ranked research university is currently searching for a Clinical Research Coordinator III for one of its growing departments to be for all study-related activities including screening & consent and enrollments, data collection/entry, and compliance with the regulatory process.
Responsibilities:
Ref: #558-Scientific
Location: Pittsburgh, PA, Hybrid: Combination of On-Campus or Remote determined by the department.
Schedule: Varied based on participants schedule
Type: Direct Hire or 6 -12 month Contract based on department needs
Overview:
A top-ranked research university is currently searching for a Clinical Research Coordinator III for one of its growing departments to be for all study-related activities including screening & consent and enrollments, data collection/entry, and compliance with the regulatory process.
Responsibilities:
- 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.
#M3
Ref: #558-Scientific