Community IBC Member (Augusta)
Sitero LLC•Augusta, GA
•$110 - $125•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.
Requirements
- Advanced degree or equivalent experience in science, medicine, research ethics, regulatory affairs, biostatistics, veterinary medicine, biosafety, or related field (requirements vary by committee).
- 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
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.
- Attendance at scheduled meetings (frequency varies by committee).
- Independent review time prior to meetings.
- Participation in ad hoc reviews or urgent matters when needed.
Benefits
- hourly rate, depending on experience
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What This Job Offers
Career Level
Mid Level
