... research community with an emphasis on ethics, compliance, and innovation. Job Title: Research ... This is a contract role paying a flat rate per meeting that is attended EMPLOYMENT TYPE: Contractor ...
... research community with an emphasis on ethics, compliance, and innovation. Job Title: Research ... This is a contract role paying a flat rate per meeting that is attended EMPLOYMENT TYPE: Contractor ...
... research community with an emphasis on ethics, compliance, and innovation. Job Title: Research ... This is a contract role paying and hourly rate, depending on experience. EMPLOYMENT TYPE:
... research community with an emphasis on ethics, compliance, and innovation. Job Title: Research ... This is a contract role paying and hourly rate, depending on experience. EMPLOYMENT TYPE:
Adjunct, Physician Assistant
Duluth, MN · On-site
$1.1K/wk
Any future updates to per credit rates of pay will be reflected within the electronic contract. Job ... research, ethics and/or public health. Adjunct faculty are hired on a course by course basis as ...
Adjunct, Physician Assistant
Duluth, MN · On-site
$1.1K/wk
Any future updates to per credit rates of pay will be reflected within the electronic contract. Job ... research, ethics and/or public health. Adjunct faculty are hired on a course by course basis as ...
Dean of Instruction and Institutional Research
Monterey, CA · On-site
$157.84 - $179.80/hr
... research ethics standards, federal and state regulations, and institutional policies governing ... Faculty Load, Assignments, and Contract Processes * Provide leadership for operational processes to ...
New
Dean of Instruction and Institutional Research
Monterey, CA · On-site
$157.84 - $179.80/hr
... research ethics standards, federal and state regulations, and institutional policies governing ... Faculty Load, Assignments, and Contract Processes * Provide leadership for operational processes to ...
New
Oncology Research Liaison
Springfield, IL · On-site
$63K - $95K/yr
Establish relationships with trial sponsors and Contract Research Organizations (CRO's) to ... Provide excellent customer service and adhere to Springfield Clinic's Code of Conduct and Ethics ...
Oncology Research Liaison
Springfield, IL · On-site
$63K - $95K/yr
Establish relationships with trial sponsors and Contract Research Organizations (CRO's) to ... Provide excellent customer service and adhere to Springfield Clinic's Code of Conduct and Ethics ...
Oncology Research Liaison
$24 - $32/hr
Establish relationships with trial sponsors and Contract Research Organizations (CRO's) to ... Provide excellent customer service and adhere to Springfield Clinic's Code of Conduct and Ethics ...
Oncology Research Liaison
$24 - $32/hr
Establish relationships with trial sponsors and Contract Research Organizations (CRO's) to ... Provide excellent customer service and adhere to Springfield Clinic's Code of Conduct and Ethics ...
Lead efforts to secure research funding, grants, and contracts. * Encourage and support faculty ... Research Ethics and Compliance: * Ensure adherence to ethical standards and regulatory requirements ...
Lead efforts to secure research funding, grants, and contracts. * Encourage and support faculty ... Research Ethics and Compliance: * Ensure adherence to ethical standards and regulatory requirements ...
Lead efforts to secure research funding, grants, and contracts. * Encourage and support faculty ... Research Ethics and Compliance: * Ensure adherence to ethical standards and regulatory requirements ...
Lead efforts to secure research funding, grants, and contracts. * Encourage and support faculty ... Research Ethics and Compliance: * Ensure adherence to ethical standards and regulatory requirements ...
Clinical Research Associate
Irvine, CA · Remote
$120K - $135K/yr
The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... ethics documents, such as IRB/EC submissions, contracts, and site feasibility questionnaires.
Clinical Research Associate
Irvine, CA · Remote
$120K - $135K/yr
The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... ethics documents, such as IRB/EC submissions, contracts, and site feasibility questionnaires.
Lead efforts to secure research funding, grants, and contracts. * Encourage and support faculty ... Research Ethics and Compliance: * Ensure adherence to ethical standards and regulatory requirements ...
Lead efforts to secure research funding, grants, and contracts. * Encourage and support faculty ... Research Ethics and Compliance: * Ensure adherence to ethical standards and regulatory requirements ...
Clinical Research Associate
Irvine, CA · On-site
$120K - $135K/yr
The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... ethics documents, such as IRB/EC submissions, contracts, and site feasibility questionnaires.
Clinical Research Associate
Irvine, CA · On-site
$120K - $135K/yr
The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... ethics documents, such as IRB/EC submissions, contracts, and site feasibility questionnaires.
Clinical Research Coordinator II - Artificial Intelligence & Human Health Research - (Bi-Lingual Spa
Manhattan, NY · On-site
$26.75 - $35.50/hr
... and Contracts Office). We are seeking a highly motivated and organized Clinical Research ... Familiarity with IRB processes, research ethics, and HIPAA compliance (preferred). About Us ...
Clinical Research Coordinator II - Artificial Intelligence & Human Health Research - (Bi-Lingual Spa
Manhattan, NY · On-site
$26.75 - $35.50/hr
... and Contracts Office). We are seeking a highly motivated and organized Clinical Research ... Familiarity with IRB processes, research ethics, and HIPAA compliance (preferred). About Us ...
Lead efforts to secure research funding, grants, and contracts. * Encourage and support faculty ... Research Ethics and Compliance: * Ensure adherence to ethical standards and regulatory requirements ...
Lead efforts to secure research funding, grants, and contracts. * Encourage and support faculty ... Research Ethics and Compliance: * Ensure adherence to ethical standards and regulatory requirements ...
Dean of Instruction and Institutional Research
Monterey, CA · On-site
$14K - $16K/mo
... research ethics standards, federal and state regulations, and institutional policies governing ... Faculty Load, Assignments, and Contract Processes Provide leadership for operational processes to ...
Dean of Instruction and Institutional Research
Monterey, CA · On-site
$14K - $16K/mo
... research ethics standards, federal and state regulations, and institutional policies governing ... Faculty Load, Assignments, and Contract Processes Provide leadership for operational processes to ...
This unique role supports compliance with research ethics and regulatory requirements while ... This does not constitute an employment contract. Minimum Qualifications * Bachelor's degree in ...
This unique role supports compliance with research ethics and regulatory requirements while ... This does not constitute an employment contract. Minimum Qualifications * Bachelor's degree in ...
$108K - $153K/yr
... Research ... Ethics Boards, Contract, and Training, developing process improvements. * Contributing to the ...
$108K - $153K/yr
... Research ... Ethics Boards, Contract, and Training, developing process improvements. * Contributing to the ...
Clinical Research Manager
Lowell, MA · On-site
The role may include oversight of internal Clinical Research Associates and/or external contract ... Support and contribute to ethics committee and IRB submissions, renewals, supplements, and ...
Quick apply
Clinical Research Manager
Lowell, MA · On-site
The role may include oversight of internal Clinical Research Associates and/or external contract ... Support and contribute to ethics committee and IRB submissions, renewals, supplements, and ...
Sr. Clinical Study Manager
Naples, FL · On-site
Must have a strong understanding of federal regulations relating to clinical studies (FDA, MDR), ISO, and research ethics. * Experience in managing research contracts and protocol development is ...
Sr. Clinical Study Manager
Naples, FL · On-site
Must have a strong understanding of federal regulations relating to clinical studies (FDA, MDR), ISO, and research ethics. * Experience in managing research contracts and protocol development is ...
Sr. Clinical Study Manager
Naples, FL · On-site
Must have a strong understanding of federal regulations relating to clinical studies (FDA, MDR), ISO, and research ethics. * Experience in managing research contracts and protocol development is ...
Sr. Clinical Study Manager
Naples, FL · On-site
Must have a strong understanding of federal regulations relating to clinical studies (FDA, MDR), ISO, and research ethics. * Experience in managing research contracts and protocol development is ...
Research Operations Lead
New York, NY · On-site
... and vendor contracts. You approach every workflow with a clarifying question: what truly needs ... Define our research ethics and data governance standards. Own the frameworks, consent workflows ...
Research Operations Lead
New York, NY · On-site
... and vendor contracts. You approach every workflow with a clarifying question: what truly needs ... Define our research ethics and data governance standards. Own the frameworks, consent workflows ...
Contract Research Ethics information
What are the most commonly searched types of Research Ethics jobs? The most popular types of Research Ethics jobs are:
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.
About Sitero
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
11 - 50 Employees
Headquarters location
Miami, FL, US
Year founded
1999