Community IBC Member (Augusta)

Sitero LLC

Augusta (GA)

On-site

USD 41,328 - 68,880

Part time

14 days+
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Job summary

Sitero LLC is seeking a Research Compliance Committee Member for a contract role focused on reviewing research protocols for compliance with regulatory and ethical standards. In this remote position, you will evaluate risks and ensure the safety and integrity of research participants.

The role requires an advanced degree in science or a related field along with demonstrated knowledge of research regulations. Previous experience in compliance or oversight committees is preferred. Competitive hourly compensation will be provided based on experience.

Qualifications

  • Advanced degree or equivalent experience in relevant fields.
  • Demonstrated knowledge of research regulations and ethical principles.
  • Prior service on compliance or oversight committees.

Responsibilities

  • Review research submissions for compliance standards.
  • Prepare and participate in scheduled meetings.
  • Evaluate risks and identify non-compliance issues.
  • Document reviews following institutional policies.

Skills

Knowledge of research regulations
Ethical principles
Regulatory oversight experience
Human subjects protection training

Education

Advanced degree in science or related field

Job description

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.

Job Title: Research Compliance Committee Member

Location: Remote

Function: Delivery

ESSENTIAL DUTIES AND RESPONSIBILITIES

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.

Core 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.
Institutional Biosafety Committee (IBC)
  • 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.
EDUCATION REQUIRED
  • Advanced degree or equivalent experience in science, medicine, research ethics, regulatory affairs, biostatistics, veterinary medicine, biosafety, or related field (requirements vary by committee).
EXPERIENCE REQUIRED
  • 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.
COMPENSATION & BENEFITS

This is a contract role paying and hourly rate, depending on experience.

EMPLOYMENT TYPE

Contractor

COMMITMENTS
  • Attendance at scheduled meetings (frequency varies by committee).
  • Independent review time prior to meetings.
  • Participation in ad hoc reviews or urgent matters when needed.
DISCLAIMER

Sitero is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.

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