Weekend Irb Jobs in California (NOW HIRING)

Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care. Primary Duties & Responsibilities: * Works with a Clinical ...

This role will comply with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care. Job Duties and Responsibilities: Works with a Clinical Research ...

Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission ...

Serve as a primary point of contact for sponsors, CROs, and IRB communications * Prepare and submit regulatory documents, including IRB submissions, amendments, and continuing reviews * Monitor ...

Serve as a primary point of contact for sponsors, CROs, and IRB communications * Prepare and submit regulatory documents, including IRB submissions, amendments, and continuing reviews * Monitor ...

Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission ...

Serve as a primary point of contact for sponsors, CROs, and IRB communications * Prepare and submit regulatory documents, including IRB submissions, amendments, and continuing reviews * Monitor ...

This role will comply with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care. Job Duties and Responsibilities: Works with a Clinical Research ...

Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities * Independent ...

IRB), pharmaceutical companies (including monitors), principal investigators and colleagues. Works with clinical trial coordinators, research staff and investigators to further communications ...

Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities * Independent ...

Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with ...

IRB), pharmaceutical companies (including monitors), principal investigators and colleagues. Works with clinical trial coordinators, research staff and investigators to further communications ...

Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities * Independent ...

Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...

Provides increasingly complex and independent support for studies by serving as the independent contact with sponsors, IRB, and research participants, providing training, education to junior level ...

Facilitate communication with appropriate site staff involved in start-up and IRB/EC submissions * Facilitate site budget and site contract negotiations and ensure timely finalization of the required ...

Notifies Director, sponsor and IRB of any serious adverse events. * Assist physician with all procedures to include excisions, injections, laser treatments, wound care, post-op care and dressing ...

Notifies Director, sponsor and IRB of any serious adverse events. * Assist physician with all procedures to include excisions, injections, laser treatments, wound care, post-op care and dressing ...

Notifies Director, sponsor, and IRB of any serious adverse events. * Assist the physician with all procedures, including excisions, injections, laser treatments, wound care, post-op care, and ...