Clinical Research Coordinator
Carnegie, Pennsylvania
Employer: System One Holdings, LLC
Industry:
Salary: Competitive
Job type: Full-Time
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. If interested in joining this dynamic department, please apply!
Responsibilities:
Requirements:
Job Title: Clinical Research Coordinator
Location: Pittsburgh, PA, Hybrid: Combination of On-Campus and Remote work
Schedule: Mon - Fri 8am to 5pm
Type: Direct Hire
Responsibilities:
Requirements:
#M3
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. If interested in joining this dynamic department, please apply!
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:
Job Title: Clinical Research Coordinator
Location: Pittsburgh, PA, Hybrid: Combination of On-Campus and Remote work
Schedule: Mon - Fri 8am to 5pm
Type: Direct Hire
Responsibilities:
- Work closely with the Principal Investigators, study/clinical staff assisting in the operations of ongoing clinical trials.
- Responsibilities for:
- 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.
- Recruit research subjects/conduct interviews and research assessments.
- Assists with Institutional Review Board renewal, modification, and approved protocols.
Requirements:
- Bachelor's Degree - any major
- Prefer 1 year of relevant experience (trials preferred but would also consider other medical documentation experience
- Demonstrate a high degree of professionalism/discretion
- Strong attention to detail
#M3
Created: 2024-09-06
Reference: 323996
Country: United States
State: Pennsylvania
City: Carnegie
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