20 Best Vice President jobs in Brooklyn, NY (Hiring Now!)

VP, Regulatory Affairs
Scismic —New York, NY
Ensure that sound regulatory practices are fully integrated into pre-clinical, clinical and technical submissions, and will ensure that all documents submitted…
$325,000 - $330,000 a year
2d
Associate Vice President of Integrated Health
Heartshare Human Services Of New York —Brooklyn, NY
Collaborate with the Director & Community Partnership Coordinator to develop new partnership leads for referral sources with the goal of recruiting clients…
$120,000 - $125,000 a year
Quick Apply
Sales Assistant to VP of Sales (Wholesale Jewelry Company)
JAY GEMS —Long Island City, NY
Bachelor's degree in Business Administration or related field preferred. Assist with pricing strategies and customer proposals.
$18 - $22 an hour
Quick Apply
1d
VP, Clinical Development – Solid Tumor
Scismic —New York, NY
Minimum of 5 years of oncology experience – strongly prefer clinical research experience be mostly in the field of oncology.
$360,000 - $420,000 a year
2d
Vice President, Residential National Accounts (Builders)
Overhead Door Corporation —United States
The objective is to develop relationships enabling us to become the single point of contact with these national builders and ultimately drive our products sales…
$175,000 - $300,000 a year
Quick Apply
Vice President, Development
GOSO - GETTING OUT AND STAYING OUT INC. —New York, NY
Bachelor’s degree in development, marketing, business administration, or related field required. We work with all interested individuals, regardless of the…
$130,000 - $140,000 a year
Quick Apply
VP of Pricing & Analytics (Supply Chain)
GENPRO INC —Rutherford, NJ
Lane cost analysis, establish cost and service-related processes. Genpro is looking for a VP of Pricing & Analytics who will assist the company in driving sales…
Estimated: $62.9K - $79.6K a year
Quick Apply
VP - Business Development Manager (Full-time, New York)
The Commercialiser —New York, NY
Convert viable prospects into active clients, owning the full sales process from lead generation to negotiation and close, through to the transition of new…
Up to $100,000 a year
Quick Apply
Bank Relationship Manager ( Associate to VP) Japanese Bilingual
Pasona N A, Inc. —New York, NY
Sales promotion of banking products and services to corporate clients in accordance with the bank’s and department’s strategy and direction.
$157,000 a year
Quick Apply
Regional VP Business Development- HealthCare / Skilled Nursing
Genesis HealthCare —Montclair, NJ
Use Genesis Core Operating System (PCC) to analyze inquiries, admissions, discharges, sales calls and other information , to communicate with Sales, Marketing…
Estimated: $67.4K - $85.3K a year
Quick Apply
13d
Modern Workplace Engineer - M365 Portfolio Manager, VP
MUFG Bank, Ltd. —Jersey City, NJ
Ability to explain key end-user solutions and technical architecture aligned to the firm’s maturity framework/path in Office 365, Windows, and tools such as…
$145,000 - $182,000 a year
Vice President, Facilities
The Dermot Company —New York, NY
A professional engineering or related license is a plus. Minimum of five (5) years of having full oversight of a portfolio of multifamily assets and mentoring…
$170,000 - $210,000 a year
Quick Apply
Vice President, Acquisition
Morgan Stanley —New York, NY
Requires four (4) years of experience with: producing financial models and valuation on companies and assets; analyzing a business from an investor’s…
Estimated: $151K - $191K a year
4h
Vice President
Morgan Stanley —New York, NY
Requires five (5) years of experience with: designing and managing Events and conference workflows for an Investment Bank for their Corporate Access, Research,…
Estimated: $155K - $197K a year
Vice President - Labor Relations
MCR Hotels —New York, NY
Leading the labor initiatives to ensure compliance with all applicable federal, state, and local laws and lead collective bargaining negotiations.
$180,000 - $230,000 a year
13d
VICE PRESIDENT OF OPERATIONS
Flik Hospitality Group —New York, NY
Holiday Time Off (varies by site/state). ServSafe or Department of Health certification a plus. Develops and monitors realistic and accurate budget and…
$175,000 a year
Quick Apply
13d
Assistant Vice President, Materials Management
NYC Health + Hospitals —New York, NY
A. Develops a procurement plan and strategy to reduce and contain costs; evaluates and assists in vendor selection; ensures excellent supplier performance;…
$220,000 a year
Vice President for Strategy and Communication
Citizens Budget Commission —New York, NY
The VP will provide strategic guidance into CBC’s focus areas and spearhead advocacy; be responsible for the production, impact, positioning, distribution,…
$170,000 - $210,000 a year
Quick Apply
6d
Vice President, Marketing
Soko Glam —Brooklyn, NY
Bachelor's degree in Marketing, Business Administration, or related field; MBA preferred. As Vice President of Marketing at Soko Glam, you will spearhead our…
$180,000 - $240,000 a year
Quick Apply
Vice President of House Calls (must have Healthcare experience, P&L & Home based care a plus))
Essen Healthcare —Bronx, NY
Create and implement reporting of KPIs in the field to measure performance and enforce accountability, inclusive of the identification of 5-8 KPI’s that aim to…
$150,000 - $200,000 a year
Quick Apply

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VP, Regulatory Affairs

Scismic New York, NY

Apply Now

Job Details

Full-time $325,000 - $330,000 a year 2 days ago

Benefits

Health insurance
401(k)
Paid time off
Vision insurance
401(k) matching

Qualifications

Biotechnology
Medicine
Clinical research
Doctoral degree
Clinical development
Regulatory reporting
11+ years
GMP
Master's degree
Analysis skills
Compliance management
Drug discovery
Doctor of Philosophy
Good Clinical Practice
Oncology
Leadership
Communication skills
FDA regulations
10 years

Full Job Description

Scismic is supporting the growth of a late-stage, publicly traded biopharmaceutical company developing targeted radiotherapies to deliver cancer-killing radiation with cellular level precision to treat patients with high unmet medical needs.

Their vision is to build a specialty, hospital-focused radiotherapeutics company that develops and markets medicines for relapsed or refractory cancer patients who are treated primarily in large quaternary care hospitals and their catchment areas. On the basis of results that demonstrate meaningful survival benefit and provide the opportunity to move the goal post in AML, the company intends to launch two drugs in five years.

The company is well-funded. Their differentiated product pipeline is further exemplified by their next-generation program for rapidly growing cell and gene therapies, as well as their solid tumor and immunotherapy collaborations with several large companies. In addition, they have several other programs in solid tumors at the pre-clinical stage with IND-enabling studies ongoing and their extensive intellectual property portfolio includes over 200 issued patents and pending patent applications worldwide.

Job Overview:

The incoming VP of RA will be a leader and key member of a dynamic team who is responsible for developing, directing and implementing the regulatory strategy for several programs with a focus on unmet medical needs in oncology. The VP will identify the key strategic regulatory drivers for early and late stage programs for submissions (from IND to BLA) to US and international regulatory agencies. This position also will be responsible for developing, establishing and maintaining effective relationships with regulatory agencies, especially the FDA, EMA and overseeing all Regulatory Affairs activities. The incoming candidate must have significant regulatory expertise in Oncology drug development with a demonstrated track record of success in terms of biologics drug approvals.

This role reports to CMO.

Key Responsibilities:

Develop and implement Regulatory Affairs strategies and tactical work plans during clinical development and in preparation for the anticipated US filings.
Identifying and assessing regulatory risks, understanding global imperatives including market-related drivers.
Accountability for overseeing regulatory submissions for the oncology portfolio, including the associated communication strategy to all regulatory authorities.
Ensure that sound regulatory practices are fully integrated into pre-clinical, clinical and technical submissions, and will ensure that all documents submitted to regulatory agencies are appropriately reviewed to ensure they are complete, scientifically accurate, and of high quality.
Contribute to the creation and implementation of development plans that incorporate regulatory strategies designed to maximize the likelihood of successful regulatory applications, delivering regulatory approval and reimbursement for all key indications.
Act as a credible, influential, respected spokesperson during interactions with US and international regulatory agencies, and ensure appropriate, proactive communication with agencies to assure expedient and efficient review and approval of submissions.
Monitor and anticipate regulatory & Scientific Advances, novel end-points, innovative clinical trial designs and regularly brief company management.
Present and defend regulatory plans to Senior Management.
Lead the preparation and management of timely regulatory submissions, including INDs, briefing documents, clinical protocols, BLAs, fast-track/breakthrough/accelerated approval/orphan drug applications.
Fulfill all requirements for ensuring all reporting obligations are met, including amendments, annual reports to FDA, safety and quality reports.
Collaborate with Medical to manage the regulatory aspects of the company Pharmacovigilance system including the establishment and review of SOPs and providing the regulatory oversight of the system managements and reporting requirements.
Collaborate with Product Development, Manufacturing and Quality to manage regulatory aspects of all CMC activities. Perform regulatory evaluation of CMC change controls.
Participate or lead regulatory interactions with and presentations to US FDA and other regulatory agencies.
Review and approval of Clinical Study Protocols, Clinical Study Reports, Statistical Analysis Plans, and ISS.
Represent Regulatory Affairs on cross-functional teams. Interact collaboratively with CMC, clinical, pre-clinical, supply chain, operations and other functional management as they impact the quality of products and operations.
Evaluate and approve documentation for regulatory filings.
Use considerable analytical and judgment skills to drive continuous improvements.
Hybrid work schedule: 2-3 days in office are required.

Qualifications:

MS/PhD or MD in Life/Health Sciences.
A proven leader with a minimum of 10+ years pharmaceutical/biotechnology industry experience in multiple phases of development (must have both large and small company experience), 10+ years regulatory experience in biotech programs.
MUST HAVE BIOLOGICS EXPERIENCE
Recent experience of IND, NDA and BLA submissions a must.
Deep knowledge and understanding of drug development process, regulatory requirements and environment, especially in the US.
Demonstrate strategic thinking and implementation in overall drug development, with experience in orphan diseases.
Demonstrated strategic capability and ability to see the overall, 'big' picture, along with examples of showing courage and confidence to lead and implement change.
Ability to read, analyze and interpret complex regulatory documents and to respond effectively to sensitive inquiries or complaints.
Able to drive strategic thinking and plans for successful regulatory outcomes.
Dynamic individual with excellent written and communication skills.
Ability to set priorities, work independently and deliver results in a timely manner.
Experience in interfacing with regulatory authorities.
Strong planning, organizational and leadership skills.
Strong interpersonal skills and the ability to skillfully and appropriately manage, develop and mentor personnel in a matrix environment.
Attention to detail.
Thorough understanding of the FDA (biologics division), including experience in PAI readiness.
Results oriented. Strong initiative, accountability and willingness to take ownership and drive projects to completion.
Experience in radiopharmaceuticals is a major plus.

Compensation will be commensurate with experience. The company offers competitive base salaries, performance bonuses, equity incentive plans, 401(K) with company matching and comprehensive health benefits.

Job Type: Full-time

Pay: $325,000.00 - $330,000.00 per year

Benefits:

401(k)
Health insurance
Paid time off

Experience level:

11+ years

Schedule:

Monday to Friday

Work Location: Hybrid remote in New York, NY 10017

Apply Now

Vice President jobs in Brooklyn, NY

VP, Regulatory Affairs

Associate Vice President of Integrated Health

Sales Assistant to VP of Sales (Wholesale Jewelry Company)

VP, Clinical Development – Solid Tumor

Vice President, Residential National Accounts (Builders)

Vice President, Development

VP of Pricing & Analytics (Supply Chain)

VP - Business Development Manager (Full-time, New York)

Bank Relationship Manager ( Associate to VP) Japanese Bilingual

Regional VP Business Development- HealthCare / Skilled Nursing

Modern Workplace Engineer - M365 Portfolio Manager, VP

Vice President, Facilities

Vice President, Acquisition

Vice President

Vice President - Labor Relations

VICE PRESIDENT OF OPERATIONS

Assistant Vice President, Materials Management

Vice President for Strategy and Communication

Vice President, Marketing

Vice President of House Calls (must have Healthcare experience, P&L & Home based care a plus))

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