Chairperson

Company Information

At Advarra, we are passionate about making a difference in the world of clinical research and advancing human health. With a rich history rooted in ethical review services combined with innovative technology solutions and deep industry expertise, we are at the forefront of industry change. A market leader and pioneer, Advarra breaks the silos that impede clinical research, aligning patients, sites, sponsors, and CROs in a connected ecosystem to accelerate trials.

Our employees are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.

At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each employee is not only valued but empowered to thrive and make a meaningful impact.

Advarra has as its core function the institutional review board (IRB) review of a broad spectrum of research ranging from survey research to first-in-human research and sponsored by pharmaceutical companies, biotech companies, institutions, hospitals as well as clinics and private physician offices. The regulatory group is responsible for the expedited review of research, the full board review of research and the documentation of the meeting minutes.

The regulatory group also collaborates with other parts of the organization on thought leadership, client guidance and operational efficiencies.

At Advarra, the Chairperson leads discussion at full board meetings and ensures that reviews are completed in accordance with Advarra policy and appropriate regulations. This position works with the Chair Director, Senior Chair Director(s), and the Institutional Official (IO) to ensure that Advarra effectively fulfills its obligation to help protect human research subjects.

• Maintain superior level knowledge of regulatory requirements, Advarra’s board standard operating procedures, and organizational policies.
• Act as a point of contact for Advarra operations staff, assisting with day-to-day challenges
• Chair one or more weekly meetings.
• Complete expedited reviews for minimal risk research, continuing reviews, investigational brochure updates, and prompt reporting events.
• Respond to protocol and informed consent questions for minimal risk or full board protocols.
• Ensure appropriate triaging of submissions for minimal risk or full board review.
• Review amendments for scientific and non-scientific requirements.
• Oversee pre-review of protocols.
• Identify areas for guidance and inconsistencies in Board reviews.
• Participate in clinically and regulatory-oriented teleconferences.
• Consult with sponsors, investigators, and CROs on clinical and regulatory affairs.
• Attain and maintain necessary regulatory knowledge for medical device reviews.
• Work with Chair Director(s) to identify membership needs and develop board members.
• Assist in the annual evaluation of board members.
• Onboard and train new unaffiliated board members.
• Perform co-chair duties during chairperson onboarding.
• Foster a work atmosphere focused on accountability, motivation, team building, training, mentoring, collaboration, and respect.
• Identify qualified resources for the board to ensure adequate review expertise.

This role is open to candidates working remotely in the United States.

• Bachelor’s degree in a related field.
• 1+ years of service chairing IRB meetings or similar experience; 3+ years of experience with an institutional IRB or research experience with a healthcare or clinical research entity within the last 6 years.
• Advanced knowledge of all regulations and guidance pertinent to human subject protection in the United States and Canada including, but not limited to AAHRPP, FDA, OHRP, and ICH.
• Moderate computer skills including experience with MS Office products.
• Certified IRB Professional (CIP) certification within 2 years of employment.

• Graduate degree (MS, MA, MD, PhD, DO, etc)
• Advanced knowledge of all regulations and guidance pertinent to human subject protection in the United States and Canada including, but not limited to AAHRPP, FDA, OHRP, and ICH.
• Moderate computer skills including experience with MS Office products.
• Certified IRB Professional (CIP) certification within 2 years of employment.

• Sit or stand for extended periods of time at stationary workstation.
• Regularly carry, raise, and lower objects of up to 10 Lbs.
• Learn and comprehend basic…