
Senior Counsel, Assistant Vice President of Legal Affairs, Clinical Research & Regulatory Compliance
- West Orange, NJ
- Permanent
- Full-time
- The Senior Counsel, Assistant Vice President of Legal Affairs, Clinical Research & Regulatory Compliance reports directly to the Vice President of Legal Affairs.
- Juris Doctor from an accredited law school
- Active license to practice law in the State of New Jersey or eligibility for in-house counsel licensure in NJ
- Minimum of 8 years of legal experience, including substantial experience with clinical research, FDA regulatory compliance, and research contracting
- Comprehensive knowledge of federal research regulations, including FDA, HHS, OHRP, and NIH guidelines
- Demonstrated ability to manage complex agreements and collaborate effectively with operational, academic, and compliance stakeholders,
- Experience supporting an academic medical center, research institute, or life sciences sponsor
- Working knowledge of intellectual property, technology transfer, and conflicts of interest in research
- Draft, negotiate, and review clinical trial agreements, research collaboration agreements, material transfer agreements, data use agreements, sponsored research agreements, and associated amendments
- Provide legal advice on budgeting, intellectual property, publication rights, indemnification, confidentiality, subject injury, and other key research contract terms
- Coordinate with investigators, research administration, compliance, and finance to ensure timely execution and alignment with institutional policies and sponsor requirements
- Advise on laws and regulations applicable to human subject research, including FDA regulations -21 CFR Parts 50, 56, 312, and 812, the Common Rule - 45 CFR Part 46, and HIPAA Privacy Rule as it applies to research
- Support the Institutional Review Board in navigating complex regulatory questions involving informed consent, privacy protections, and multi-site trial oversight
- Counsel stakeholders on Good Clinical Practice, FDA inspection readiness, and compliance with ClinicalTrials, gov registration and reporting requirements
- Ensure institutional compliance with research-related components of the Uniform Guidance - 2 CFR Part 200, NIH Grants Policy Statement, and other federal and state funding agency rules
- Provide legal advice on cost allocation, effort reporting, and subrecipient monitoring requirements
- Assist in resolving audit findings, responding to federal inquiries, and guiding corrective action plans related to research compliance
- Develop and maintain template research agreements and regulatory guidance materials
- Conduct legal training for researchers, IRB staff, and research administrators on evolving legal standards and institutional protocols
- Track and assess new federal and state legislative and regulatory developments affecting research and provide timely legal interpretation to stakeholders
- Paid Time Off including Vacation, Holidays, and Sick Time
- Retirement Plans
- Medical and Prescription Drug Insurance
- Dental and Vision Insurance
- Disability and Life Insurance
- Paid Parental Leave
- Tuition Reimbursement
- Student Loan Planning Support
- Flexible Spending Accounts
- Wellness Programs
- Voluntary Benefits (e.g., Pet Insurance)
- Community and Volunteer Opportunities
- Discounts Through our Partners such as NJ Devils, NJ PAC, and Verizon
- ….and more!