Community IBC Member (Augusta)

Sitero LLC•Augusta, GA

4d•Remote

About The Position

Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation. The Research Compliance Committee Member serves as a subject-matter contributor responsible for reviewing research protocols, monitoring regulatory compliance, and ensuring protection of research participants, animals, data integrity, and biosafety standards. The role supports ethical, scientific, and regulatory oversight across multiple institutional review and monitoring committees. Members are expected to apply regulatory knowledge, professional judgment and independence to ensure institutional and federal compliance standards are met.

Requirements

Demonstrated knowledge of research regulations and ethical principles.
Prior service on compliance or oversight committees.
Regulatory or clinical research experience.
Training in human subjects protection, animal welfare, biosafety, or data monitoring.

Nice To Haves

Advanced degree or equivalent experience in science, medicine, research ethics, regulatory affairs, biostatistics, veterinary medicine, biosafety, or related field (requirements vary by committee).

Responsibilities

Review research submissions for regulatory, ethical, and institutional compliance.
Prepare for and actively participate in scheduled meetings.
Evaluate risks, benefits, and safeguards within research protocols.
Identify non-compliance, protocol deviations, or safety concerns.
Maintain confidentiality of sensitive research information.
Provide recommendations for approval, modification, suspension, or termination of studies.
Document reviews and determinations in accordance with institutional policies.
Complete required training and conflict-of-interest disclosures.
Review research involving recombinants or synthetic nucleic acids, biohazards, and infectious agents.
Assess containment levels, laboratory safety procedures, and personnel protections.
Ensure adherence to biosafety regulations and institutional biosafety manuals.
Evaluate incident reports and corrective actions.
Recommend risk mitigation strategies for hazardous biological work.