Top 706 Associate director Jobs in Plainfield Nj

Associate Director, PV Strategic Partner Management
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $153,600 - $230,400 a year
- Nursing
- Office
- Master's degree
Associate Director of Technology and Data
Community Charter School of Paterson —Paterson, NJ
- $90,000 - $100,000 a year
- Full-time
- School experience
- Google Workspace
- Computer Science
- Paid time off
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7d
Associate Director, Medical Communications and Publications, HEOR Publications
Genmab —Princeton, NJ
- $162,640 - $243,960 a year
- Online Application
- 5 years
- Office
- Doctor of Philosophy
- Commuter assistance
- Paid parental leave
Associate Director, Biostatistics (Late Stage)
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $168,000 - $252,000 a year
- 5 years
- Office
- Master's degree
Associate Director, Global Market Research
BioNTech AG —Berkeley Heights, NJ
- $146,300 - $234,100 a year
- Full-time
- Background check
- Office
- 3 years
- Health savings account
- AD&D insurance
Associate Director, Supportive Housing & Services, Homeless Veterans Program
Tunnel To Towers Foundation —Staten Island, NY
- $85,000 - $95,000 a year
- Full-time
- Background check
- Master of Social Work
- Management
- 403(b) matching
- Health insurance
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Associate Director of Nursing
Skilled Nursing of Brooklyn —Brooklyn, NY
- $150,000 - $170,000 a year
- Full-time
- RN License
- Mid-level
- 3 years
Quick Apply
9h
Associate Director, Business Performance - Neuroscience
Novartis —East Hanover, NJ
- $145,600 - $270,400 a year
- Full-time
- Hybrid work
- 6 years
- Office
- Finance
- Health insurance
- 401(k) matching
Associate Director, US Brand Marketing
CSL Seqirus —Summit, NJ
- $180,000 - $205,000 a year
- Full-time
- 7 years
- Marketing
- Analysis skills
Associate Director, Medical Writing
Genmab —Princeton, NJ
- $160,080 - $240,120 a year
- Online Application
- English
- Microsoft Office
- Analysis skills
- Commuter assistance
- Paid parental leave
Associate Executive Director
Montclair YMCA —Montclair, NJ
- $65,000 - $75,000 a year
- Full-time
- Office
- 3 years
- Ability to lift 50 pounds
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Associate Program Director- Outpatient Treatment
Remedy Recruitment, LLC —Newark, NJ
- $67,500 a year
- Full-time
- Licensed Clinical Social Worker
- LPC
- Mid-level
- Health savings account
- Health insurance
Quick Apply
1d
Associate Director - External Data Acquisition Lead (EDAL)
Genmab —Plainsboro, NJ
- $157,360 - $236,040 a year
- Online Application
- Master's degree
- Bachelor's degree
- Mentoring
- Commuter assistance
- Paid parental leave
14d
Associate Director, Biostatistics
Genmab —Princeton, NJ
- $156,880 - $235,320 a year
- Online Application
- Master's degree
- Databases
- Doctor of Philosophy
- Commuter assistance
- Paid parental leave
Associate Director, Medical Affairs Capabilities, Strategic Planning & Effectiveness
Genmab —Princeton, NJ
- $156,880 - $235,320 a year
- Online Application
- Office
- 3 years
- Finance
- Commuter assistance
- Paid parental leave
1d
Associate Director Biostatistics
Penfield Search Partners —Princeton, NJ
- $1 - $2 an hour
- Full-time
- Hybrid work
- 5 years
- Office
- Continuous improvement
Quick Apply
14d
Associate Director, Statistical Programming
Everest Clinical Research —Bridgewater, NJ
- $170,000 - $205,000 a year
- Remote
- Computer Science
- 11+ years
- Databases
- AD&D insurance
- Disability insurance
Quick Apply
Associate Director; Private Equity Fund Accounting (East Coast Region)
SS&C Technologies —New York, NY
- $90,000 - $205,000 a year
- Online Application
- CPA
- 3 years
- Master's degree
- Paid holidays
- Health insurance
Associate Director, Data Science - Market Access
Sanofi EU —Morristown, NJ
- $148,500 - $214,500 a year
- 5 years
- Bachelor of Science
- Office
- Parental leave
Associate Director Biostatistics
Penfield Search Partners —Princeton, NJ
- $185,000 a year
- Hybrid work
- 5 years
- Office
- Continuous improvement
Quick Apply

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Associate Director, PV Strategic Partner Management

Daiichi Sankyo, Inc. -
Basking Ridge, NJ

Apply Now

Job Details

$153,600 - $230,400 a year

Qualifications

Bachelor's degree
Pharmaceutical company experience
Clinical quality assurance standards

Full Job Description

Job Title:
Associate Director, PV Strategic Partner Management

Job Requisition ID:
1455

Posting Start Date:
5/4/26

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.

Job Summary

Oversees Local/Global Pharmacovigilance (PV) service providers responsible for Call Center, individual safety case processing, and aggregate reporting for DSI products, both investigational and marketed. Maintains compliance with Global PV regulations for individual case safety and periodic reporting. Serves as the key DSI contact for PV service providers to address, escalate issues requiring attention or resolution, and proactively drive operational excellence and continuous improvement. Manage DSI's Strategic PV Partnerships and contracts including vendor outsourcing agreements, PV Agreements (PVAs) and Safety Data Exchange Agreements (SDEAs). Maintains oversight of DSI contracts that are PV relevant and AE reporting language in associated contractual templates. Ensures Good Pharmacovigilance Practice and regulatory compliance in such arrangements. Oversees the management of PV Regulatory Intelligence (PVRI) and dissemination across CSPV stakeholders for impact assessment. Participates in the review and management of monthly, quarterly, and ad hoc PVRI reports received from CSPV vendors.

Responsibilities

Strategic Partner Management: Oversees Local/Global PV service providers responsible for Call Center, individual safety case processing, and aggregate reporting

Establish and maintain collaborative relationships with key stakeholders within CSPV and external functions including Clinical Development, Research & Development, Regulatory Affairs

Facilitate operational meetings with CROs, License Partners, and PV vendors

Provide PV oversight of the DSI Call Center

Provide oversight of ICSR processing activities including, Safety Information submission to Health Authorities and License Partners, Reconciliation with License Partners, Patient Support Programs, Market Research vendors, Global Quality Supply Chain, Medical Information Social Media and other suppliers

Ensure adequate training of resources to enable quality of deliverables.

Manage quality, efficiency, and resources for PV service providers/vendors

Measure and monitor performance of vendors against service level and KPIs

Develop governance, business continuity, quality, and vendor monitoring plans

Maintain oversight for capability development of service provider and resources

Plan, allocate, and utilize resources and prioritize assignments

Manage and escalate issues for resolution

Coordinate vendor assessments and make recommendations on vendor partners

Coordinate PV participation in due diligence for acquisitions and divestments

Negotiate and organize transfer of PV Business in case of Product Divestment

Collaborate with DSI audit groups to ensure comprehensive auditing of Business Partners as required to assure compliance with PV agreements

Participate in audit and inspection readiness activities

Provide input for remediating PV system deficiencies cited in audit/inspections

Implement effective corrective and preventative action PV Agreements and Contracts: Manages PVAs/SDEAs and maintains oversight of PV relevant contracts

Oversee and set standards for PV contract management.

Review & contribute to revision of DSI contracts under negotiation (e.g. development, license, distribution agreements)

Manage, negotiate, revise & document collaborative & license partner safety agreements with counterparts from (license) partner companies

Responsible for development and maintenance of a PVA repository

Lead development of standard processes and contract templates in cooperation with Legal Department and PV functions

Drive development of standards for information exchange with partners in cooperation with PV functions

Initiate the implementation of obligations deriving from these contracts

Organize and conduct periodic review of contract quality and adherence PV Regulatory Intelligence:

Oversees the Management of PV Regulatory Intelligence and dissemination across CSPV stakeholders for impact assessment.

Participates in the review and management of monthly, quarterly, and ad hoc PV regulatory intelligence reports received from CSPV vendors. Management Strategy and Goals: Assist CSPV Leadership in developing PV goals, continued compliance, and strategy for process improvement initiatives.

Qualifications

Education Qualifications

Bachelor's Degree in nursing, pharmacy, life sciences, health care or related field; required. A higher-level degree such as a PharmD or Master's Degree in life sciences preferred

Experience Qualifications

Musthave a minimum of 4 or more years of professional pharmaceutical industry experience in PV management.

Proven knowledge of Drug Safety/Pharmacovigilance experience, including both investigational and marketed products

Must have strong knowledge of Good Clinical Procedures (GCP) and Good Pharmacovigilance Procedures (GVP)

Knowledge of FDA regulations, clinical and safety databases; preferred

Experience with Good Clinical Procedures (GCP) and Good Pharmacovigilance Procedures (GVP) preferred

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Salary Range:
USD$153,600.00 - USD$230,400.00

Download Our Benefits Summary PDF

Professionals

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Refine Your Search

associate director jobs in plainfield nj

Associate Director, PV Strategic Partner Management

Associate Director of Technology and Data

Associate Director, Medical Communications and Publications, HEOR Publications

Associate Director, Biostatistics (Late Stage)

Associate Director, Global Market Research

Associate Director, Supportive Housing & Services, Homeless Veterans Program

Associate Director of Nursing

Associate Director, Business Performance - Neuroscience

Associate Director, US Brand Marketing

Associate Director, Medical Writing

Associate Executive Director

Associate Program Director- Outpatient Treatment

Associate Director - External Data Acquisition Lead (EDAL)

Associate Director, Biostatistics

Associate Director, Medical Affairs Capabilities, Strategic Planning & Effectiveness

Associate Director Biostatistics

Associate Director, Statistical Programming

Associate Director; Private Equity Fund Accounting (East Coast Region)

Associate Director, Data Science - Market Access

Associate Director Biostatistics

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