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Clinical Bioethics Jobs in Boston, MA (NOW HIRING)

... disorders in clinical care (R01DA062848). The postdoctoral researcher will be part of an ... Strong interest in neuroethics, bioethics, health policy, economics, genomics, and/or related areas.

Clinical Bioethics information

See Boston, MA salary details

$15

$37

$97

How much do clinical bioethics jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical bioethics in Boston, MA is $37.61, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $35.77 per hour, depending on experience, location, and employer.

What is clinical bioethics?

A Clinical Bioethics job involves analyzing ethical issues in healthcare, such as patient rights, medical decision-making, and policy development. Professionals in this field work in hospitals, research institutions, or ethics committees to guide healthcare providers and patients through complex ethical dilemmas. They often help interpret ethical principles, assist in policy creation, and provide education on bioethical concerns.

What does a typical day look like for someone working in clinical bioethics?

A typical day in Clinical Bioethics often involves consulting with healthcare providers, patients, and families to address complex ethical dilemmas that arise in patient care. You might participate in ethics committee meetings, review and develop hospital policies, and provide educational sessions or workshops for staff. Collaboration is frequent, as you’ll work with interdisciplinary teams—such as physicians, nurses, and social workers—to help ensure that patient care decisions are ethically sound. The work environment is usually hospital-based, and the role may require both structured case consultations and on-call responsibilities.

What are the key skills and qualifications needed to thrive in clinical bioethics?

To thrive in Clinical Bioethics, a strong background in healthcare or philosophy—often supported by an advanced degree in bioethics, ethics, or a related field—is essential. Familiarity with ethics consultation documentation systems, research databases, and relevant bioethics certifications (such as HEC-C) is frequently required. Critical thinking, excellent communication, and the ability to mediate complex discussions are crucial soft skills. These capabilities ensure ethically sound decision-making and effective guidance in challenging clinical situations.

How do I become a clinical bioethicist?

To become a clinical bioethicist, typically a master's or doctoral degree in bioethics, healthcare, philosophy, or a related field is required. Relevant experience in healthcare settings, strong ethical reasoning skills, and certification from professional organizations can enhance qualifications. Many clinical bioethicists work in hospitals, academic institutions, or healthcare organizations, often requiring knowledge of medical practices and ethical guidelines.

What do clinical bioethicists do?

Clinical bioethicists analyze ethical issues in healthcare settings, providing guidance on complex cases involving patient rights, informed consent, and medical decision-making. They often collaborate with medical staff, patients, and families, and may develop policies or conduct ethics consultations to support ethical practices in clinical environments.

What cities near Boston, MA are hiring for Clinical Bioethics jobs?

Cities near Boston, MA with the most Clinical Bioethics job openings:

Infographic showing various Clinical Bioethics job openings in Boston, MA as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 18% Part Time, and 7% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $78,223 per year, or $37.6 per hour.

Postdoctoral Research Fellow

Bioethics.net

Boston, MA • On-site

$60 - $90/hr

Other

Posted 4 days ago


Job description

Postdoctoral Research Fellow (ELSI)

Please submit your CV, cover letter, and 2 writing samples to HTPLab@mgb.org. Priority Deadline: July 15, 2026.

The Health Technology Performance Lab (HTP Lab) in the Department of Neurosurgery at Mass General Brigham is hiring a full‑time postdoctoral researcher to help execute an NIH‑funded study examining the ethical, clinical, legal, and healthcare systems challenges and potential solutions associated with the use of genetic tests for substance use disorders in clinical care (R01DA062848). The postdoctoral researcher will be part of an interdisciplinary team of researchers led by Gabriel Lázaro‑Muñoz, PhD, JD, Amanda Merner, PhD, and Theresa Williamson, MD, MPH. The role offers opportunities to lead publications, present research at conferences, and receive mentoring on grant writing.

Key Responsibilities Leadership, Training, and Program Development
  • Oversee study operations and assist with coordinating all study activities between the lab and external collaborators.
  • Assist with development of standard operating procedures and quality assurance systems for the study.
  • Contribute to creation of study templates, database management, and training materials for new study staff.
  • Assist with training and mentoring entry‑level CRCs and study interns, ensuring adherence to the lab’s standard operating procedures and best practices.
Study Coordination and Execution
  • Work with study PIs to manage day‑to‑day study activities, including recruitment, coordination and scheduling of study interviews, and coordination of team meetings.
  • Develop and maintain project timelines, recruitment benchmarks, and operational workflows.
  • Lead data collection (semi‑structured interviews, surveys, chart reviews) and quality control checks using REDCap, EPIC, and other programs.
  • Assist with/lead instrument development for semi‑structured interviews and experimental surveys.
  • Lead data analysis (qualitative interview data and quantitative survey data) using Dedoose, Excel, R, and other programs.
  • Assist with/lead preparation of manuscripts and presentations to disseminate study findings.
Regulatory and Compliance
  • Prepare and maintain Institutional Review Board (IRB) protocol submissions, amendments, and continuing reviews.
  • Ensure compliance with study protocols, Human Subjects and Good Clinical Practice guidelines, and institutional policies.
  • Prepare progress reports for key stakeholders and funders.
Qualifications Education & Experience
  • Doctoral degree (PhD, MD, LD) required; genetics, health sciences, social sciences, psychology, public health, neuroscience, or related field preferred.
  • Strong track record of executing human subjects research including direct experience with IRB/regulatory documentation.
  • Experience with building recruitment and data collection pipelines to execute both qualitative and quantitative data collection.
  • Experience analyzing and reporting findings from mixed‑methods studies, including qualitative data analysis and quantitative data analysis.
  • Experience preparing manuscripts for publication.
  • Strong interest in neuroethics, bioethics, health policy, economics, genomics, and/or related areas.
Skills & Competencies
  • Ability to oversee and train others effectively.
  • Strong organizational, time‑management, and problem‑solving skills.
  • Demonstrate a high degree of flexibility in accepting work assignments with the ability to effectively prioritize tasks, understand processes, and resolve issues.
  • Excellent interpersonal and written/verbal communication skills.
  • Ability to work independently and collaboratively across multiple investigators and teams.
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