Jennifer A. Graf
Experienced Global Ethics & Compliance, Clinical Development, and Patient Engagement Professional
- Role
- Continuing Education Program Faculty at Boston College
- Location
- Cambridge, MA, US
- LinkedIn followers
- 500 followers
About Jennifer A. Graf
Accomplished professional in Global Ethics & Compliance (E&C) and Patient Engagement (PE) with deep academic and pharmaceutical R&D experience across multiple therapeutic areas and functions. I bring a proven record of successfully embedding and implementing effective, compliant, and sustainable healthcare compliance programs. My broad expertise includes evaluating HCP and patient engagements, conducting risk assessments of complex and ambiguous global R&D business and clinical development challenges and providing actionable strategic guidance, and developing and delivering training initiatives with a focus on continuous improvement. I also have direct experience partnering with global cross-functional teams to embed impactful patient and caregiver/partner perspectives into clinical strategies, ensuring that development plans are scientifically sound and patient-centered. My extensive hands-on experience in research ethics includes informed consent and assent, regulatory interpretation, bioethics, IRB management, COI adjudication, and auditing & monitoring. Known for translating complex challenges into pragmatic solutions, I deliver timely results through strong collaboration, clear communication, and trusting relationships. I bring a unique combination of practical experience and strategic insight to drive meaningful, high-quality results in the evolving pharmaceutical landscape.
Experience
Continuing Education Program Faculty
Jan 2012 — Present
Clinical Research Continuing Education (bioethics, ethical evaluation of human research, informed consent & assent, privacy).
Education
Seton Hall University School of Law
Completed Healthcare Compliance Certification Program
Wheaton College Massachusetts
BA
Skills
- Conflict of Interest
- Lifesciences
- Irb
- Quality Improvement
- Clinical Trials
- Hipaa
- Regulatory Analysis
- Fda
- Sop Development
- Clinical Study Design
- Compliance
- Clinical Research
- Institutional Review Board (Irb)
- Policy Writing
- Life Sciences
- Gcp
- Research Ethics
- Quality Assurance
- Research
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