Research Compliance Analyst

HRPP- Human Research Protection Program

Seeking Research Analyst to join our team! Is that you?

Work location: 8440 Walnut Hill Lane Dallas, TX 75231

Work hours: Full Time Monday through Friday 7:00am – 6:00pm with a flexible start and end time.

Department highlights:

• Fantastic work environment
• Opportunities for growth
• In depth human research program
• Working closely with an integrated team
• Opportunities to affect change in research operations and to provide education to the research community

Here’s What You Need

• A Bachelor's Degree in science or related field OR 4 Years IRB and or HRPP regulatory experience, research administration experience, or other relevant experience in lieu of a degree is required.
• 2 Years of Research, IRB regulatory or research administration experience is required
• CIP (Certified IRB Professional) Upon Hire is preferred

What You Will Do

• Receives and reviews IRB submissions for completeness and compliance with IRB policy, institutional requirements, and State/Federal regulations.
• Manages and processes human subject research applications. Conducts pre-review of submissions requiring IRB review to ensure completeness and compliance with regulations and THR policies.
• Will provide approval/release of submission to the appropriate IRB for review. Review protocols that meet the regulatory criteria for exemption and make exemption determinations, as appropriate.
• Serve as a subject matter expert in regard to HRPP. Provide advice, guidance and problem resolution to Investigators and support personnel about regulations, guidelines and THR policies and procedures concerning protection of human subjects.
• Assist in conducting training and education of researchers.
• Serve as principal point of contact/liaison to both internal customers (e.g., investigators, research administration, legal counsel, etc.) and external customers (e.g. study sponsors, IRB staff, federal and state oversight agencies, etc.) on professional and operational matters pertaining to the HRPP.
• Develop and maintain positive relationships with collaborating organizations and commercial IRBs. Provide direction to researchers regarding protocol submission and deficiencies in submission, informed consent document, etc.
• Other duties and special projects as assigned. Ensure THR clinical trial website is up to date. Compile of data and reports as related to research activity as requested.

Additional perks of being a Texas Health Nurse

• Benefits include 401k, PTO, medical, dental, Paid Parental Leave, flex spending, tuition reimbursement, student Loan forgiveness as well as several other benefits.
• A supportive, team environment with outstanding opportunities for growth.
• Explore our Texas Health careers site for info like Benefits, Job Listings by Category, recent Awards we’ve won and more.

Do you still have questions or concerns? Feel free to email your questions to recruitment@texashealth.org.

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