Lead IRB Coordinator
TEPHRA
Description:
Lead IRB Coordinator West Reading, Pennsylvania
Flexible work from home days
Required to be on site at least one day per week (at Reading Hospital location).
Responsibilities:
Reports to the Director, Human Subject Protections (Director) and works closely with the IRB Coordinator I, Chair and members of the Institutional Review Board (IRB).
Responsible for pre-review of items submitted for review by the IRB to confirm compliance with institutional, federal, and state policies.
Communicates with research investigators and their staff in an effort to facilitate the protocol submission, review and approval process.
Qualifications:
Education Requirements
4 year Bachelor's Degree - OR - combination of relevant education & experience may be considered in lieu of Bachelor's Degree
Experience
IRB Manager Experience Preferred
Post Approval Monitoring Experience Preferred
Broad Research Administration Experience Preferred
Certification and Licensure
CIP certification (must obtain within 1 year of hire)
Required Skills
Excellent Communications Skills
Excellent Interpersonal Skills
General Clerical Skills
Multitasking
Medical Terminology
Computer Skills to include use and navigation
Customer Service Skills
Detail Oriented
Problem Solving Skills
Organizational Skills
Good Reasoning Skills
Microsoft Office Applications
Part-time
Benefits - Full
Relocation Assistance Available - Possible for ideal candidate
Interview Travel Reimbursed - Yes
CANDIDATE DETAILS
2+ to 5 years experience
Lead IRB Coordinator West Reading, Pennsylvania
Flexible work from home days
Required to be on site at least one day per week (at Reading Hospital location).
Responsibilities:
Reports to the Director, Human Subject Protections (Director) and works closely with the IRB Coordinator I, Chair and members of the Institutional Review Board (IRB).
Responsible for pre-review of items submitted for review by the IRB to confirm compliance with institutional, federal, and state policies.
Communicates with research investigators and their staff in an effort to facilitate the protocol submission, review and approval process.
Qualifications:
Education Requirements
4 year Bachelor's Degree - OR - combination of relevant education & experience may be considered in lieu of Bachelor's Degree
Experience
IRB Manager Experience Preferred
Post Approval Monitoring Experience Preferred
Broad Research Administration Experience Preferred
Certification and Licensure
CIP certification (must obtain within 1 year of hire)
Required Skills
Excellent Communications Skills
Excellent Interpersonal Skills
General Clerical Skills
Multitasking
Medical Terminology
Computer Skills to include use and navigation
Customer Service Skills
Detail Oriented
Problem Solving Skills
Organizational Skills
Good Reasoning Skills
Microsoft Office Applications
Part-time
Benefits - Full
Relocation Assistance Available - Possible for ideal candidate
Interview Travel Reimbursed - Yes
CANDIDATE DETAILS
2+ to 5 years experience
Vacancy posted 1 day ago
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