Joulé
Clinical Research Coordinator III
Joulé, Carnegie, Pennsylvania, United States, 15106
Job Title: Clinical Research Coordinator III
A high number of candidates may make applications for this position, so make sure to send your CV and application through as soon as possible. Location: Pittsburgh, PA, Hybrid: Combination of On-Campus and Remote work as determined by the department. Schedule: varied including evening, overnight, and weekend hours Type: Direct Hire
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.
Requirements: Minimum Education Requirement: Bachelor’s Degree Experience Requirement: At least 3-5 years of clinical trial/clinical research experience 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
A high number of candidates may make applications for this position, so make sure to send your CV and application through as soon as possible. Location: Pittsburgh, PA, Hybrid: Combination of On-Campus and Remote work as determined by the department. Schedule: varied including evening, overnight, and weekend hours Type: Direct Hire
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.
Requirements: Minimum Education Requirement: Bachelor’s Degree Experience Requirement: At least 3-5 years of clinical trial/clinical research experience 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