Clinical Research Coordinator at System One Pittsburgh, PA

kozmetickesluzby.vecnakraska.sk - Jobboard; Pittsburgh (Allegheny County); Hybrid; USD 50,000 - 70,000; Full time

Benefits offered by this job

Health Insurance

Dental Insurance

Vision Insurance

401(k) Plan

Job summary

kozmetickesluzby.vecnakraska.sk is seeking a Clinical Research Coordinator in Pittsburgh, PA. This role involves coordinating clinical trials, screening patients, and managing informed consent processes. A Bachelor's degree and relevant experience in clinical research are essential.

The position offers hybrid work with a combination of on-campus and remote work. Benefits include health, dental, vision, and a 401(k) plan. Interested candidates are encouraged to apply!

Qualifications

• Minimum education requirement is a Bachelor's Degree.
• 1+ years of direct clinical research experience is preferred.
• CRC certification is preferred but not required.

Responsibilities

• Coordinate study activities and work closely with Principal Investigators.
• Screen patients for eligibility and conduct informed consent discussions.
• Adhere to IRB protocols and conduct research assessments.

Skills

Clinical Research

Patient Screening

IRB Protocols

Education

Bachelor's Degree

Tools

Clinical Trial Management Systems

Job description

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

• 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.

Benefits

System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

Equal Opportunity Employer

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.