Mount Sinai Morningside · 2 days ago
Associate Director of Operations - Center for Interventional Cardiovascular Research and Clinical Trials
New York, NY
Full-time
Onsite
Lead/Staff, Director/Executive
$80K/yr - $161K/yr
5+ years expMount Sinai Morningside is a leading academic medical center seeking an Associate Director of Operations to oversee daily operational, administrative, and research activities of the department. This role involves providing leadership across staff supervision, budgetary oversight, and ensuring compliance while advancing the Center’s strategic growth through innovative technology and data analytics.
Hospital & Health Care
Responsibilities
Lead all administrative operations, managing a multidisciplinary team supporting clinical trials, registries, and translational research
Provide day-to-day supervision of the Clinical Trial Management Team, Administration Team, and Catheterization Laboratory Research Team
Assist the Director in daily departmental operations and provide professional and administrative guidance to staff
Evaluate operational performance and identify opportunities for improvement; advise and inform the Director of administrative issues, needs, and risks
Plan, organize, and implement services to meet departmental goals and objectives
Develop, implement, and refine departmental policies, procedures, and SOPs to ensure efficiency, quality, and regulatory compliance
Oversee hiring, supervision, mentoring, evaluation, and retention of administrative and research staff
Foster a culture of accountability, inclusivity, collaboration, and professional development
Participate in interviewing and recommending candidates; assist with onboarding, orientation, mentoring, training, and probationary and annual evaluations
Recommend recognition, disciplinary actions, and termination when necessary
Maintain staff competencies through ongoing training and professional development initiatives
Ensure compliance with IRB, FDA, GCP, ICH, and institutional policies and standards
Review and assist with regulatory submissions, including IRB/IEC packages and continuing reviews
Conduct regular reviews of the Trial Master File (TMF) to ensure inspection readiness
Review monitoring visit reports and collaborate with monitors to address data quality, compliance trends, and site issues
Manage and coordinate assigned clinical research studies to ensure adherence to protocols, SOPs, and regulatory requirements
Coordinate clinical trial schedules, staff assignments, and subject management activities
Oversee subject enrollment, tracking, and completion of required regulatory documentation
Support study design, including review and/or development of protocols, informed consent forms (ICFs), and related study documents
Contribute to the development of Case Report Forms (CRFs)
Plan and conduct site evaluations, initiations, and routine monitoring visits; maintain strong relationships with clinical sites
Plan, organize, and present at investigator meetings
Serve as the primary point of contact for CROs and clinical vendors; provide study status updates, enrollment metrics, safety trends, and recommendations
Assist in the preparation, planning, and management of departmental and study budgets
Perform financial reconciliations, cost variance analyses, and budget justifications
Recommend and implement cost-effective operational strategies
Contribute to the development and negotiation of study budgets and contracts; ensure effectiveness of site budget and contract processes
Provide oversight and accountability for all third-party vendors
Drive cross-departmental collaboration to enhance research delivery, scalability, and impact
Collaborate with faculty and scientific leadership to identify emerging research opportunities and partnerships
Support investigators in preparing high-quality research submissions, including budgets, biosketches, letters of support, and compliance documentation
Manage the full proposal lifecycle, including feasibility assessments, RFP responses, bid defenses, and submissions
Leverage advanced data analytics, digital platforms, and AI-driven tools to streamline operations and improve decision-making
Champion predictive analytics, machine learning, and decision-support systems to optimize research performance and forecasting
Perform other related duties as assigned
Qualification
Required
Bachelor's degree in public health/administration or business or a related field or equivalent education and experience; Masters (MPA, MPH, MBA or related) is preferred
5 years of experience in a professional business environment, with health related and project management experience preferred
Supervisory experience is a plus; 1 year in CRO, Pharma, Biotech or ARO preferred
Company
Mount Sinai Morningside
At Mount Sinai Morningside, we offer exceptional clinical care and research within the comfort of a neighborhood hospital known for compassion and sensitivity.
1001-5000 employees
H1B Sponsorship
Mount Sinai Morningside has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (5)
2024 (3)
2023 (26)
2022 (20)
2021 (6)
2020 (20)
Funding
Current Stage
Late StageLeadership Team
Faye Reiff-Pasarew
Deputy CMO, Associate Chief of Hospital Medicine, Assistant Professor of Internal Medicine
Lucy Xenophon, MD, MPH
Chief Transformation Officer
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