Sitero
Community IBC Member (Augusta)
Augusta, Georgia, United States · Contract
Sponsorship not specifiedDetected 6 days ago
ComplianceClinical TrialsClinical ResearchFDA RegulatoryResearchBiostatisticsRegulatory Affairs
About the role
- 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.
- Members are expected to apply regulatory knowledge, professional judgment, and independence to ensure institutional and federal compliance standards are met.
- Core Responsibilities: Review research submissions for regulatory, ethical, and institutional compliance.
Responsibilities
- The role supports ethical, scientific, and regulatory oversight across multiple institutional review and monitoring committees.
- Maintain confidentiality of sensitive research information.
- Document reviews and determinations in accordance with institutional policies.
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.
- Complete required training and conflict-of-interest disclosures.
Compensation
- This is a contract role paying and hourly rate, depending on experience.
Benefits
- Evaluate risks, benefits, and safeguards within research protocols.
Equal opportunity
- Sitero is an equal opportunity employer and welcomes all job applicants.
- equal opportunity employer and welcomes all job applicants.
This listing is sourced directly from Sitero's careers page and normalized into a canonical job model.