What are the responsibilities and job description for the Senior Regulatory Coordinator (Clinical Research) position at APR Consulting?
APR Consulting, Inc. has been engaged to identify a Senior Regulatory Coordinator
Location: Los Angeles, CA 90025
Position: Senior Regulatory Coordinator
Pay Rate: $48.50/hr
Duration: 13 weeks
Expected Shift: 40 hrs/week
8am to 5pm
JOB SUMMARY
***This is a senior-level role. Must have previous work history in a Regulatory role to qualify. This is not a role for a CRC or CRA to transition into regulatory work***
Required Qualifications: (Must be reflected on resume)
• Bachelor’s degree
• 3 years in the field of clinical research and as a Regulatory Coordinator/Specialist
• Experience with applicable regulations, institutional policies, Standard Operating Procedures (SOPs), and study-specific protocols/plans and processes
• Working knowledge of Institutional Review Board (IRB) & Contracts and Grants policies and procedures.
• Experience in writing research correspondence to IRB and study sponsors.
• Experience with submitting continuations and amendments to regulatory bodies.
• Experience tracking regulatory documents (including lab certifications, CV’s, IRB compliance and correspondence letters, medical licenses, FDA Forms, Delegation of Authority Forms, Serious Adverse Event submissions, etc.)
• Experience with FDA Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) as well as Local Institutional Review Board (IRB) regulatory requirements.
• Working knowledge of informed consent forms to ensure compliance with applicable laws and Institutional policies.
Preferred Qualifications:
• 1 years oncology experience
• CCRP certification
• Epic Experience
Our client is the one of the largest Healthcare Staffing Provider in the United States, to be assigned at one of their affiliated hospitals/healthcare facilities.
This particular client is requiring that all new hires show proof of vaccination. However, accommodations may be made for those with disabilities or religious reasons who cannot obtain a vaccine.
Since 1980 APR Consulting, Inc. has provided professional recruiting and contingent workforce solutions to a diverse mix of clients, industries, and skill sets nationwide.
We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
Don't miss out on this amazing opportunity! If you feel your experience is a match for this position please apply today and join our team. We look forward to working with you!
Location: Los Angeles, CA 90025
Position: Senior Regulatory Coordinator
Pay Rate: $48.50/hr
Duration: 13 weeks
Expected Shift: 40 hrs/week
8am to 5pm
JOB SUMMARY
***This is a senior-level role. Must have previous work history in a Regulatory role to qualify. This is not a role for a CRC or CRA to transition into regulatory work***
Required Qualifications: (Must be reflected on resume)
• Bachelor’s degree
• 3 years in the field of clinical research and as a Regulatory Coordinator/Specialist
• Experience with applicable regulations, institutional policies, Standard Operating Procedures (SOPs), and study-specific protocols/plans and processes
• Working knowledge of Institutional Review Board (IRB) & Contracts and Grants policies and procedures.
• Experience in writing research correspondence to IRB and study sponsors.
• Experience with submitting continuations and amendments to regulatory bodies.
• Experience tracking regulatory documents (including lab certifications, CV’s, IRB compliance and correspondence letters, medical licenses, FDA Forms, Delegation of Authority Forms, Serious Adverse Event submissions, etc.)
• Experience with FDA Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) as well as Local Institutional Review Board (IRB) regulatory requirements.
• Working knowledge of informed consent forms to ensure compliance with applicable laws and Institutional policies.
Preferred Qualifications:
• 1 years oncology experience
• CCRP certification
• Epic Experience
Our client is the one of the largest Healthcare Staffing Provider in the United States, to be assigned at one of their affiliated hospitals/healthcare facilities.
This particular client is requiring that all new hires show proof of vaccination. However, accommodations may be made for those with disabilities or religious reasons who cannot obtain a vaccine.
Since 1980 APR Consulting, Inc. has provided professional recruiting and contingent workforce solutions to a diverse mix of clients, industries, and skill sets nationwide.
We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
Don't miss out on this amazing opportunity! If you feel your experience is a match for this position please apply today and join our team. We look forward to working with you!
Salary : $49