Pediatric Clinical Research Associate II — Bioethics Focus

3M HEALTHCARE; Memphis (TN); On-site; USD 71,000 - 127,000; Full time

Job summary

St. Jude Children's Research Hospital seeks a Clinical Research Associate II or Clinical Research Associate II RN to join its Bioethics Program on site in Tennessee.

The role supports data abstraction, collection, and entry for clinical research, along with coordinating with study sponsors and ethics committees. Responsibilities include coordinating participant recruitment, consent, data documentation, and preparation of reports.

Qualifications

• Bachelor's degree in a relevant area is required.
• Master's degree preferred, ideally in bioethics or related field.
• Minimum 2+ years of experience in carrying out research, preferably healthcare.

Responsibilities

• Act as site study coordinator recruiting participants and assisting with protocol submissions for review by committees.
• Develop, maintain, monitor, and share documentation (investigator files, case report forms, study data).
• Perform data abstraction, collection, and entry to support clinical research.
• Conduct interviews and focus groups with study participants.
• Prepare submissions for reportable events (adverse events, protocol variances).
• Prepare detailed data reports as required.
• Provide patient care, education, and management related to protocol activities.
• Engage in literature reviews and synthesize findings.
• Assist in grant preparation and manuscript submissions.
• Participate in research manuscript preparation and submissions.

Skills

Data abstraction

Clinical research

Informed consent

Literature reviews

Education

Bachelor's degree (clinical research)

Master's degree preferred (bioethics)

Job description

St. Jude Children's Research Hospital seeks a Clinical Research Associate II or Clinical Research Associate II RN to join its Bioethics Program on site in Tennessee.

The role supports data abstraction, collection, and entry for clinical research, along with coordinating with study sponsors and ethics committees. Responsibilities include coordinating participant recruitment, consent, data documentation, and preparation of reports.