Logo for Sitero

Community IBC Member (Nashville, TN)

Role overview

Qualifications

  • Advanced degree or equivalent experience in science, medicine, research ethics, regulatory affairs, biostatistics, veterinary medicine, biosafety, or related field
  • Demonstrated knowledge of research regulations and ethical principles
  • Prior service on compliance or oversight committees
  • Regulatory or clinical research experience

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

About the company

Sitero logo

Sitero

Contract Research Organizations (CRO)

Sitero is a next-generation, site-focused clinical research organization (CRO) for life sciences and institutional research organizations that helps get treatments to market safer and faster through tech-forward services that streamline research. Accelerate your clinical trial, drive compliance and safety, and unlock innovation with access to powerful technology and world-class services. Sitero combines the expertise of a tenured team with a nimble, innovative approach to clinical research. Sitero has offices in the U.S., U.K., and India.

Company details

Company typeSME
IndustryContract Research Organizations (CRO)
Company size51 - 200

Your match analysis

See how your profile stacks up against this role.

We compared the job requirements to your profile to show where you're strong and where you fall short.

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: Nashville, TN area 

Function: Research Compliance



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 a flat rate per meeting that is attended


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.


Compensation: $110-125 per meeting

Apply once. Then go straight to the hiring manager.

After you apply, unlock the direct contact details of the people who actually make the call. A quick follow-up makes you 5x more likely to land an interview.

MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
Unlocked after you apply
·

Related jobs

Other jobs at Sitero

Premium

Reach out to the hiring manager directly.

Gain access to the contact details of the hiring managers who actually decide, and reach out to network with them directly. That, plus more when you upgrade:

  • Full match report with fit score and gaps
  • Career diagnostics on how recruiters read you
  • Curated company matches and warm intros
  • 48h early access to new roles

Cancel anytime.