Regulatory Coordinator, Central Research
Northside Hospital is award-winning, state-of-the-art, and continually growing.
Constantly expanding the quality and reach of our care to our patients and communities creates even more opportunity for the best healthcare professionals in Atlanta and beyond.
Discover all the possibilities of a career at Northside today.
Coordinates regulatory requirements integral to the conduct of clinical research.
Ensures regulatory and organizational compliance in the compilation of complete, accurate, organized critical documents for physicians, study sponsors, Contract Research Organizations, and Institutional Review Boards.
Routinely works with sensitive or confidential information, documents and issues.
KNOWLEDGE SKILLS AND ABILITIES/LICENSE OR CERTIFICATION REQUIRED Bachelor's Degree required, preferably in a healthcare / health sciences related field with 2 years experience in clinical research or IRB functions OR Master's Degree with 1 year experience in clinical research or IRB functions.
Knowledge about clinical research administration, regulatory requirements.
Knowledge of key research regulations (e.
g.
, FDA / OHRP / ORI / DHHS / NIH) General understanding of human subject protection and Institutional Review Board regulation and operation Computer proficient in Microsoft WORD, EXCEL, ACCESS and PowerPoint applications.
Strong attention to detail and ability to adhere to policies and procedures Effective organizational skills, effective follow-through and commitment to excellence Strong interpersonal skills; ability to work with personnel at all levels to gather information, communicate compliance requirements and handle complex issues within an often-sensitive political environment Ability to work collaboratively in a team environment Must be flexible and adaptable as conditions and environment are unpredictable and change frequently Able to track multiple projects simultaneously Effective professional communication skills; ability to communicate with others in a clear, understandable and professional manner #J-18808-Ljbffr Recommended Skills Adaptability Administration Attention To Detail Clinical Research Confidentiality Coordinating Apply to this job.
Think you're the perfect candidate? Apply on company site $('.
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on('click', function (event) window.
ExternalApply = window.
open('/interstitial?jobdid=j3q3qb684wfx8m03967', 'ExternalApply-j3q3qb684wfx8m03967'); ); Estimated Salary: $20 to $28 per hour based on qualifications.
Constantly expanding the quality and reach of our care to our patients and communities creates even more opportunity for the best healthcare professionals in Atlanta and beyond.
Discover all the possibilities of a career at Northside today.
Coordinates regulatory requirements integral to the conduct of clinical research.
Ensures regulatory and organizational compliance in the compilation of complete, accurate, organized critical documents for physicians, study sponsors, Contract Research Organizations, and Institutional Review Boards.
Routinely works with sensitive or confidential information, documents and issues.
KNOWLEDGE SKILLS AND ABILITIES/LICENSE OR CERTIFICATION REQUIRED Bachelor's Degree required, preferably in a healthcare / health sciences related field with 2 years experience in clinical research or IRB functions OR Master's Degree with 1 year experience in clinical research or IRB functions.
Knowledge about clinical research administration, regulatory requirements.
Knowledge of key research regulations (e.
g.
, FDA / OHRP / ORI / DHHS / NIH) General understanding of human subject protection and Institutional Review Board regulation and operation Computer proficient in Microsoft WORD, EXCEL, ACCESS and PowerPoint applications.
Strong attention to detail and ability to adhere to policies and procedures Effective organizational skills, effective follow-through and commitment to excellence Strong interpersonal skills; ability to work with personnel at all levels to gather information, communicate compliance requirements and handle complex issues within an often-sensitive political environment Ability to work collaboratively in a team environment Must be flexible and adaptable as conditions and environment are unpredictable and change frequently Able to track multiple projects simultaneously Effective professional communication skills; ability to communicate with others in a clear, understandable and professional manner #J-18808-Ljbffr Recommended Skills Adaptability Administration Attention To Detail Clinical Research Confidentiality Coordinating Apply to this job.
Think you're the perfect candidate? Apply on company site $('.
external-apply-email-saved').
on('click', function (event) window.
ExternalApply = window.
open('/interstitial?jobdid=j3q3qb684wfx8m03967', 'ExternalApply-j3q3qb684wfx8m03967'); ); Estimated Salary: $20 to $28 per hour based on qualifications.
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