1,764 Results for

Design Director Jobs in New Jersey

Jobs

Director of Finance Vaco LLC

Northfield, NJ

Determining compensation for this role (and others) at Vaco by Highspring depends upon a wide array of factors including but not limited to: the individual’s skill sets, experience and training; licensure and certification requirements; office location and other geographic considerations; other business and organizational needs. Determining compensation for this role (and others) at Vaco/Highspring depends upon a wide array of factors including but not limited to the individual’s skill sets, experience and training, licensure and certifications, office location and other geographic considerations, as well as other business and organizational needs.

4 days ago

Electrical Design Engineer System One

Voorhees Township, NJ

$100,000–$160,000 / year
Quick Apply

This position provides you with an opportunity to develop and participate in growing our dynamic and industry leading business unit delivering system designs and solutions for utility scale power, microgrids, distributed generation systems and medium voltage electrical systems. Candidate will be expected to lead design of electrical infrastructure systems and projects, manage electrical projects, respond to Requests for Proposals, develop client and strategic client relationships.

4 days ago

Senior Director, Clinical Development Daiichi Sankyo, Inc.

Basking Ridge, NJ

$280,350–$467,250 / year
Full time

May contribute to addressing questions about medical decisions, clinical data review, protocol deviations, etc., and/or scientific aspects of the study during FDA, MHRA, EMA, and PMDA interactions, such as pre-submissions, end of phase 1/2, and inspections. 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.

30+ days ago

Senior Director, Early Clinical Development Daiichi Sankyo, Inc.

Basking Ridge, NJ

$280,350–$467,250 / year
Full time

Provides senior level clinical representation at meetings with health authorities; Leads the creation of developmental and regulatory strategy; Accountable for performance of CROs; Routine interactions with senior management of CRO, as needed; Accountable for clinical development plans, protocol profiles and sections of key submission documents; Represents Clinical Development as team leader or as supervisor of team leaders; Accountable for Clinical Development input into commercial strategy including Translational Medicine and biomarker strategy; Thought partner in driving Business Development decisions in collaboration with External Scientific Affairs dept. Study planning and execution: Develops prospective contingency plans for management of key risks across a large project or a portfolio of projects or across the Therapeutic Area; Clearly defines priorities and high-level execution plans across projects within and outside of Daiichi Sankyo; Supports effective communication and decision-making process cross-functionally and cross-regionally at department level.

6 days ago

Associate Director, Biostatistics (Late Stage Oncology) Daiichi Sankyo, Inc.

Basking Ridge, NJ

$175,440–$263,160 / year
Full time

Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis files development, statistical analysis accuracy validation, results interpretation and CSR input and review. Global BDO Strategy to Improve Drug Development: Primarily participates and may occasionally lead moderately complex initiatives, with some level of supervision, to improve the harmonization and efficiency of drug development which leads to cost savings and shortened timelines for the company.

30+ days ago

Associate Director, US Medical Affairs Training Daiichi Sankyo, Inc.

Basking Ridge, NJ

$188,640–$282,960 / year
Full time

The Associate Director, US Medical Training & Development will be responsible for ensuring Medical Affairs Teams and contingent workers have the skills and knowledge to perform effectively by developing, delivering, evaluating, and documenting training programs, including on-boarding, leadership development, therapeutic area training, skills training, and ongoing curriculum management. Primary responsibilities include: Creating and maintaining training programs for new hires and existing team members, collaborating with to align content with business goals, and transforming clinical and product information into clear, engaging training materials.

11 days ago

Director, Talent Strategy Partner Daiichi Sankyo, Inc.

Basking Ridge, NJ

$193,040–$289,560 / year
Full time

Partners closely with HR Business Partners, Centers of Excellence, and regional HR teams to deliver globally consistent yet locally relevant solutions, driving measurable impact on leadership readiness, bench strength, and performance and providing measurable business outcomes. Talent Management Together with the Head HRBPs, their teams, and senior business leaders, build the talent strategy for client groups within this role’s scope, aligning the talent strategy with the functional and enterprise business strategy, and provide input on DS’ global talent strategy.

14 days ago

Associate Director, Clinical Science Daiichi Sankyo, Inc.

Basking Ridge, NJ

$162,400–$243,600 / year
Full time

Under supervision of Clinical Science Asset Lead or Clinical Science Lead, drafts development plans, protocol profiles, protocols, informed consent forms, and sections of submission documents. Advanced Technical Expertise: Possess advanced understanding of pre-clinical and clinical research, including protocol writing, data review, study design, and disease area knowledge preferred.

30+ days ago

Director of Centralized Case Management CareOne

Fort Lee, NJ

Serve as a key liaison between centralized case management and Denials Management, ensuring timely escalation of Medicare audit findings, documentation concerns, and appeal-related issues that require case management intervention. Partner with the Denials Management lead on Medicare denials, appeals, RAC reviews, and TPE audits, providing clinical and case management support, documentation review, and operational follow-up as needed.

Today

Associate Director, Clinical Data Management Genmab

Princeton, NJ

Ensure procedures for blinding are in place where applicable - Support timely delivery of data management deliverables in accordance with Genmab SOP and ICH/GCP - Attend trial and investigator/monitor meetings as needed - Participate in definition, review and approval of data packages for Data Monitoring Committee’s, if applicable - Review and approve any corrections and updates of data packages, if applicable - Support timely development, update and maintenance of dashboards, if applicable - CRO selection and collaboration: - Support vendor qualification (Request for proposal, bid defense meetings etc.) in terms of Data management, ePRO and IRT related activities and define/specify scope of work for functional tasks - Review scope of work in a given trial in collaboration with relevant stakeholders and review/challenge major work orders (WOs)/change orders (COs)/change notification forms (CNFs) - Attend operational committee meetings, as applicable - Compliance: - Ensure compliance with relevant regulations, Genmab SOPs and ICH GCP - Ensure escalations are made as appropriate to secure proper progress and quality of the trial - Ensure compliance with Genmab Code of Business Ethics - Ensure that the trial oversight activities are conducted in accordance with the trial oversight plan, e.g. providing listings and documentation - Lead/contribute with knowledge sharing within the department - Follow scientific, process and technical progress within the field of data management in drug development and advise of new methodologies that may support innovation and improve efficiencies - Contribute on processes optimizations and SOP revisions - Lead cross-functional working groups/projects/task forces or new IT tools & technology implementation Competencies The Employee must have competences within the following areas: - - Project Management - Planning and organization - Clinical development/trial conduct, including ICH-GCP - Team leadership - Excellent communication skills and able to communicate scientific communication in clear and concise manner - Problem solving and decision making - Quality mindset - Document creation and management - Process development - Proactive and Accountable - Analytical and ability to interpret and present clinical data - IT skills Requirements Bachelor's degree in science or related area (or equivalent) 10 years of experience in clinical data management experience in biotech/ pharma industry; significant hands-on experience in all aspects of data management.

1 day ago

Associate Director - External Data Acquisition Lead (EDAL) Genmab

United States (Remote), NJ

Remote

For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.5c143e31-5e48-4549-b638-05792d185386

1 day ago

Director, Patient Services Aquestive Therapeutics Inc.

Warren, NJ

The Director of Patient Services is a strategic leadership role that owns the patient journey from prescription to therapy initiation and persistence, ensuring access translates into demand for Aquestive’s current and future portfolio, including new product launches such as Anaphylm®. Monitor payer trends, policy changes, competitive patient support trends, and innovative programs to inform strategy and proactively adjust programs to reduce emerging access barriers.

30+ days ago

Design Director Dancker

$125,000–$150,000 / year

You'll balance team development and operational oversight with hands-on engagement, mentoring, and process improvement, while guiding direct reports in project execution, resource alignment, and the delivery of accurate, timely, and high-quality design work. As a leading interior solutions provider, we seamlessly integrate architectural, furniture, technology, and logistical solutions for leading organizations across corporate, government, education, and healthcare markets.

30+ days ago

Design Director dancker

Somerville, NJ

Full time

You’ll balance team development and operational oversight with hands-on engagement, mentoring, and process improvement, while guiding direct reports in project execution, resource alignment, and the delivery of accurate, timely, and high-quality design work. As a leading interior solutions provider, we seamlessly integrate architectural, furniture, technology, and logistical solutions for leading organizations across corporate, government, education, and healthcare markets.

30+ days ago

Associate Design Director Accenture Plc

Morristown, NJ

Our capabilities span ideation to execution: growth, product and experience design; technology and experience platforms; creative, media and marketing strategy; and campaign, content and channel orchestration. With strong client relationships and deep industry expertise, we help our clients operate at the speed of life through the unlimited potential of imagination, technology and intelligence.

7 days ago

Senior Design Director - Specialized Environments Jack Morton Worldwide, Inc.

Dayton, NJ

The Senior Design Director (Specialized Environments) will play a key leadership role within the Specialized Environments practice, helping lead the creative development, design direction, and execution of high-profile environments across broadcast, branded experiences, workplace, sports, entertainment, cultural, and permanent spatial experiences. We are looking for a senior creative leader who can guide complex projects, build client confidence, mentor design teams, and help shape the future growth of the Specialized Environments group.

12 days ago

Senior Broadcast Design Director Jack Morton Worldwide, Inc.

Dayton, NJ

12 days ago

Director, Design Management CoreWeave Inc

Livingston, NJ

$198,000–$264,000 / year

Working in partnership with the Data Center Engineering and Data Center Technology teams, Design Management integrates the work of internal subject matter experts, data center providers, architects, engineers, consultants, contractors, and equipment suppliers. To conform to U.S. Government export regulations applicable to that information, applicant must either be (A) a U.S. person, defined as a (i) U.S. citizen or national, (ii) U.S. lawful permanent resident (green card holder), (iii) refugee under 8 U.S.C. § 1157, or (iv) asylee under 8 U.S.C. § 1158, (B) eligible to access the export controlled information without a required export authorization, or (C) eligible and reasonably likely to obtain the required export authorization from the applicable U.S. government agency.

30+ days ago

Optoelectronic IC Package Design Director Ciena Corp

New Providence, NJ

$235,600–$376,400 / year

Pay ranges at Ciena are designed to accommodate variations in knowledge, skills, experience, market conditions, and locations, reflecting our diverse products, industries, and lines of business. As Optoelectronic IC Package Design Director, you will be an integral part of the xPO engineering team and lead package development for custom in-house photonic, analog, and digital ICs, supporting next generation optical modules.

30+ days ago

Director of Product Design, CNBC VERSANT Media Group Inc

Englewood Cliffs, NJ

$180,000–$220,000 / year

You will work closely with product, technology, editorial, marketing and other cross-functional partners to understand customer needs, identify opportunities and create experiences that are useful, intuitive and distinctly CNBC. All resumes submitted by search firms to any employee at VERSANT via-email, the Internet, or in any form and/or method without a valid written Statement of Work in place for this position from VERSANT''s Talent Acquisition team will be deemed the sole property of VERSANT.

28 days ago

Get noticed by top employers!

Upload your resume to let employers know you're open to Design Director job opportunities. Plus, receive relevant job recommendations in your inbox.

Create A Free Account

Design Director Jobs in New Jersey

Director of Finance Vaco LLC

Electrical Design Engineer System One

Senior Director, Clinical Development Daiichi Sankyo, Inc.

Senior Director, Early Clinical Development Daiichi Sankyo, Inc.

Associate Director, Biostatistics (Late Stage Oncology) Daiichi Sankyo, Inc.

Associate Director, US Medical Affairs Training Daiichi Sankyo, Inc.

Director, Talent Strategy Partner Daiichi Sankyo, Inc.

Associate Director, Clinical Science Daiichi Sankyo, Inc.

Director of Centralized Case Management CareOne

Associate Director, Clinical Data Management Genmab

Associate Director - External Data Acquisition Lead (EDAL) Genmab

Director, Patient Services Aquestive Therapeutics Inc.

Design Director Dancker

Design Director dancker

Associate Design Director Accenture Plc

Senior Design Director - Specialized Environments Jack Morton Worldwide, Inc.

Senior Broadcast Design Director Jack Morton Worldwide, Inc.

Director, Design Management CoreWeave Inc

Optoelectronic IC Package Design Director Ciena Corp

Director of Product Design, CNBC VERSANT Media Group Inc

Similar Job Searches