Clinical Research Coordinator at System One Holdings, LLC Carnegie, PA

Comunidade Metodista; Carnegie (Allegheny County); Hybrid; USD 60,000 - 80,000; Full time

Job summary

System One Holdings, LLC in Carnegie, PA is seeking a Clinical Research Coordinator to assist in the operations of ongoing clinical trials. The role involves collaborating with PIs and study staff, screening patients for eligibility, coordinating informed consent discussions, and monitoring patient outcomes.

Applicants should have a Bachelor's degree and at least one year of direct clinical research experience; CRC certification is preferred but not required.

Qualifications

• Bachelor's degree required.
• At least 1 year direct clinical research/clinical trial experience preferred.
• CRC certification preferred but not required.

Responsibilities

• Work closely with Principal Investigators, study staff and clinical staff.
• Screen patients for eligibility and enrollment; facilitate informed consent discussions.
• Monitor patients for complications and outcomes; assist with IRB renewals and protocol adherence.

Education

Bachelor's Degree

Job description

Clinical Research Coordinator job at System One Holdings, LLC. Carnegie, PA.

Job Title: Clinical Research Coordinator
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 for one of its growing departments to be responsible for assisting in the operations of ongoing clinical trials.

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.
• 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 a year of direct clinical research/clinical trial experience is highly preferred
• 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.