IRB Board Medical Chair Physcian

Uniting Holding; Puyallup (WA); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

PTO

401K

Job summary

WIRB in Puyallup, WA is seeking an IRB Medical Board Chairperson to provide expert oversight for human subject research and ethical review. This full-time, salary position requires MD or DO and extensive IRB experience.

The role involves chairing board meetings, presenting protocols, and ensuring compliance with federal and state laws. The candidate will draft opinions, advise sponsors, and stay current with regulatory developments in medical research.

Qualifications

• MD or DO required.
• Experience in clinical research or IRB settings preferred.
• Ability to analyze complex medical and ethical issues.

Responsibilities

• Chair/Co-chair board meetings ensuring compliance with laws and policies.
• Provide scientific, ethical and regulatory support to the board.
• Analyze and present protocols and agenda items for informed decisions.
• Draft memorandums and formal opinions on exemption determinations.
• Advise clients on applicable scientific information and regulatory issues.

Skills

MS Word

MS Excel

MS Outlook

MS Windows

Education

MD or DO

Job description

The client is searching for a dedicated medical professional to join our mission of protecting human research subjects as an IRB Medical Board Chairperson in our Puyallup Washington location.

Along with a competitive salary, we also provide a robust benefits package (medical, dental, vision, PTO, 401K and more).This is a full-time, salary position.

Position Summary:

Provide the highest possible support to WIRB’s ethical review and research safety programs in areas and issues requiring medical training and judgment.

Essential Duties & Responsibilities:

• Chair / Co-chair Board meetings to ensure client’s submitted clinical research protocols are compliance with federal and state laws as well as WIRB policies and procedures.
• Facilitate discussion with other Board members.Provide scientific, ethical and regulatory support and advice.
• Analyze and present protocols and other agenda items at Board meetings to facilitate informed decision making. Set standards and role model effective presentation and discussion.
• Analyze research submissions, identify problems and issues, collect additional information or request corrections, and draft memorandums.
• Research, draft, and present reports to the Board on a wide range of topics, including but not limited to, investigator misconduct, site visits, FDA and sponsor audits of investigators and others, issues involving human subjects, sponsors, and institutions.
• Advise clients of applicable scientific information and regulations pertaining to human subject research, both orally and in writing.
• Analyze requests for exemption determinations and provide formal written opinions that proposed projects are exempt from the requirements for IRB review or do not require IRB review.
• Provide guidance to clients to help resolve scientific, ethical and regulatory issues and difficulties.
• Review literature and other materials to keep abreast of developments in the regulatory, legal, and ethical arenas.

Educational Qualifications:

• MD or DO

Qualifications/Experience Requirements:

• Able to Chair Board meeting and effectively present information to a diverse group of professionals
• Experience in clinical research, IRB, and/or similar medical ethics practices experience strongly desired
• Six or more years of related clinical experience and/or training, preferred
• Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems.
• Must not have been debarred or declared ineligible by any state or federal agency from participating in clinical research.
• Knowledge of MS Word, MS Excel, MS Outlook and MS Windows.