Compliance Officer- Administrator IV - Administration

Nathan S. Kline Institute; Blauvelt (NY); On-site; USD 95,000 - 130,000; Full time

Benefits offered by this job

Excellent Benefits Package

Job summary

Nathan S. Kline Institute is seeking a Compliance Officer to lead the institution's Research Compliance Program. You will supervise protections for human subjects and animals, data privacy, conflicts of interest, and research integrity, ensuring adherence to applicable laws and sponsor requirements.

You will partner with leadership to monitor compliance, develop policies, train staff, and manage audits and corrective actions in a dynamic regulatory environment.

Qualifications

• MA/MS degree or equivalent experience.
• 3+ years in research compliance oversight in an academic medical center.
• Knowledge of human subjects protections, regulations, and ethics.
• Experience guiding organizational compliance strategy.

Responsibilities

• Mentor compliance leads across HRPP, IACUC, biosafety, privacy and data security, and research administration.
• Audit, Monitoring & Investigations.
• Conduct annual risk assessment and compliance workplan.
• Coordinate monitoring, audits, investigations, and assessments of noncompliance.
• Liaise during internal and external audits; oversee corrective action plans.
• Develop, monitor, and report compliance metrics to leadership.
• Develop, revise, and implement research compliance policies, SOPs, and guidance documents.
• Maintain awareness of regulatory changes and ensure timely institutional updates.
• Develop and implement training programs.

Skills

Research compliance knowledge

Leadership

Policy development

Auditing abilities

Education

MA/MS degree or equivalent

Job description

JOB DESCRIPTION:

Under the general direction of the Director of NKI, the Compliance Officer (CO) provides leadership and oversight for NKI's comprehensive Research Compliance Program. The CO ensures that research activities across the institution comply with applicable federal, state, and local regulations, sponsor requirements, and institutional policies.

The CO oversees compliance across human subjects' protections, animal welfare, conflicts of interest, research integrity, bio-safety, privacy and data security, investigational drugs and devices, research billing, export controls, and grant/contract compliance. The CO promotes a culture of ethical, safe, and responsible research.

JOB DUTIES:

• Mentor compliance leads across functional areas (HRPP, IACUC, biosafety, privacy/security, research administration, etc.) to support effective operations and continuous improvement.
• Audit, Monitoring & Investigations
• Conduct and prepare an annual risk assessment and compliance workplan
• Conduct or coordinate monitoring, audits, investigations, and assessments of potential noncompliance.
• Serve as institutional liaison during internal and external audits and regulatory inspections; oversee development and implementation of corrective action plans.
• Develop, monitor, and report compliance metrics to leadership
• Policy Development & Program Enhancement
• Develop, revise, and implement research compliance policies, SOPs, and guidance documents.
• Maintain awareness of regulatory changes and ensure timely institutional updates.
• Develop and implement training programs.

Once established, the CO will proactively continue to develop new policies, programs, and procedures as needed to ensure that research compliance keeps pace with a dynamic regulatory environment and that the administration and constituents are kept aware of regulatory changes to mitigate unnecessary exposure to risk. Inherent in this work will be monitoring changes in federal regulations and state laws and, in turn, advising and educating institutional leadership, investigators, and staff on their impact on research compliance, human subject protection and animal research. The CO will ensure that research leaders and managers maintain continuously updated knowledge of current federal, state, and local regulations regarding research, including compliance with all required training and/or certifications.

JOB QUALIFICATIONS:

Minimum Qualifications:

• An M.A./M.S. Degree or equivalent related experience.
• A minimum of three years of experience in research compliance oversight in an academic medical center.
• Comprehensive knowledge of ethical issues, state laws, policies, and regulations pertaining to the protection of human research subjects.
• Demonstrated experience in guiding organizational compliance strategy, including implementing new initiatives and protocols.
• Prior experience and proven success in establishing a culture of compliance across research units.

Additionally, all candidates must be eligible to participate in Federal health care programs (e.g., Medicaid). Individuals excluded from participation in these programs will not be considered.

Preferred Qualifications:

At least one of the following: Certified IRB Professional (CIP), Certified Research Associate (CRA), Certified Clinical Research Associate (CCRA), or equivalent training or experience (such as an attorney or auditor with the necessary experience).

Background Investigation/Justice Center Review Requirements:

Prospective appointees will be: 1) Checked against the Staff Exclusion List (SEL) maintained by the Justice Center for the Protection of People with Special Needs. Prospective employees whose names appear on the SEL as having been found responsible for serious or repeated acts of abuse or neglect will be barred from appointment. 2) Screened against the Statewide Central Register of Child Abuse and Maltreatment (SCR). Prospective employees whose names are indicated on the SCR may be barred from appointment.

The Research Foundation is a private not-for-profit corporation and is not an agency or instrumentality of the State of New York. Employees of the Research Foundation are not state employees, do not participate in any state retirement system, and do not receive state fringe benefits.

Excellent Benefits Package.

Affirmative Action/Equal Opportunity Employer - Disabled/Veteran, 41 CFR 60-741.5(a) and 41 CFR 60-300.5(a) compliant.

Questions regarding this position please email: [e-mail]