Sarah Browning Email & Phone Number

Seattle, WA

• Draft, revise and maintain Institutional Review Board (IRB) policies and procedures that comply with regulatory obligations.
• Provide regulatory analysis for research protocols submitted for IRB review.
• Develop practices to include: consent form templates, privacy and confidentiality practices, review of recruitment and other study-related materials, review of clinical trial agreements, material transfer agreements.
• Provide regulatory guidance for researchers obtaining investigational drugs and devices for compassionate or emergency use under FDA rules and regulations.

Researched various Certificate of Need issues for kidney dialysis businesses.

Reviewed opposing discovery material identifying issues covered under CERCLA (over 35,000 documents).

Reviewed opposing discovery material identifying issues such as violations of responsiveness and State and Federal Medicaid laws. Assisted in depositions, the creation of interrogatories, and discovery strategy.

Created, reviewed, and updated several hundred Corporate Compliance Standards (General, Hospice, and Home Health) in order to comply with Medicaid concerns and legislation.Reviewed, modified, negotiated, and created a variety of joint venture agreements, service agreements, and technology contracts.Implemented MultiCare’s Business Associate Agreement.

• Designed, developed, and integrated hospital policies and procedures in order to more efficiently manage risk and increase compliance with changing Federal and State legislation, hospital policies, and payor practices.
• Researched and drafted memoranda on issues involving professional licensure, JCAHO accreditation, scope of practice, risk management, and regulatory compliance.

Jd, Concentration In Healthcare

Bfa, Fine Arts