1271 Associate Director And Network Architect jobs in Princeton,NJ

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Associate Director, Data Scientist

Princeton University

Princeton, NJ 08542

OnsiteUrgently Hiring

7+ years of professional experience required in an analytical or information specialist role within an academic, nonprofit, corporate or consulting setting.
Deep understanding of statistical and predictive modeling concepts, machine-learning approaches, clustering and classification techniques, and recommendation and optimization algorithms.
Keen desire to solve business problems, and to find patterns and insights within structured and unstructured data.
Expert in analyzing large, complex, multi-dimensional datasets with a variety of tools.
Accomplished in the use of statistical analysis environments such as R, MATLAB, SPSS or SAS.
Experience with BI tools such as Tableau.
Having a good understanding of relational databases, warehouse design and architecture principles.
Familiarity with big data frameworks (e.g., such as Hadoop, Hive, Spark).
Good scripting and programming skills (e.g. familiarity with SQL, Python, Java).
Strong foundation in statistical, mathematical, predictive modeling as well as business strategy skills to build the algorithms necessary to ask the right questions and find effective answers.
Familiar with disciplines such as: natural language processing, machine learning, conceptual modelling, statistical analysis, predictive modeling and hypothesis testing.
Able to create examples, prototypes, demonstrations to help management better understand the work.
Able to work autonomously.
Proficiency at planning and setting meaningful objectives to meet office goals. Ability to articulate and promote goals and implement strategic plans.
Education: Bachelor's Degree in operations research, applied statistics, data mining, machine learning, or a related quantitative discipline required.

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Associate Director, Medical Writing

Genmab

Plainsboro, NJ 08536

RemoteEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Associate Director, Medical Writing
Independently author and review complex clinical and regulatory documents, including clinical trial protocols, clinical overviews, and summaries in CTD/eCTD format for regulatory submissions.
Draft and edit more strategic documents, such as Health Authority briefing books, responses, and publications (abstracts, posters, slide presentations, and manuscripts for scientific journals).
Represent medical writing on internal teams such as the Clinical Trial Team, protocol review committee, and regulatory submission teams.
Lead submission team activities and oversee the preparation of critical documents.
Facilitate team participation in document preparation, including scheduling meetings, developing timelines, and managing document reviews and decisions.
Act as a mentor for new employees and consultants and serve as a role model for junior writers.
Lead the development and review of standard processes and templates.
Support ongoing improvements in cross-functional and global collaboration, sharing best practices and knowledge.
Maintain up-to-date knowledge of relevant regulatory guidelines and requirements.
Adhere to guidelines, SOPs, practices, and technical standards in all aspects of work.
Maintain current knowledge and competencies within relevant therapeutic and professional areas.
Contribute to knowledge sharing, skill-building, and good collaboration with stakeholders and colleagues.
Strategic thinker with a big-picture orientation.
Thorough, systematic, and organized.
Proactive, accountable, and goal oriented.
Innovative and a good team player.
Excellent at sharing knowledge and acting as a mentor.
Superior communication skills, capable of conveying scientific or medical information clearly and concisely.
Exceptional planning and coordinating abilities.
Ability to manage multiple tasks simultaneously.
Extensive knowledge of English grammar.
Expert in Microsoft 365.
Analytical skills with the ability to interpret and present clinical data and other complex information.

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Associate Director, Medical Communications and Publications, HEOR Publications

Genmab

Plainsboro, NJ 08536

Hybrid~ 12 minEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Advanced degree: PharmD, PhD, DrPH or MPH required
Certification as a Medical Publication Professional (CMPP) desirable
Knowledge of HEOR/RWE publications and strong understanding of economic modeling, RWE, epidemiological and PRO research
5+ years in medical publications, experience in HEOR, value evidence or related field within the pharmaceutical or biotech industry
Experience across all aspects of scientific publication strategy, planning and execution during all phases of drug development and commercialization process
Ability to drive and execute within a large matrix, cross-functional team, and work successfully in a fast-paced environment
Proven ability to think strategically at an enterprise level and make decisions even under conditions of ambiguity, evolving landscapes, fast paced, and tight timelines
In-depth understanding of good publication practices and guidance (GPP, ICMJE), and other guidance related to scientific data communication
Ability to travel domestically and internationally approximately 20% of time

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Associate Director - Life Sciences Advisory - Commercial

Guidehouse Careers

Philadelphia, PA 19120

New, Posted 1 day ago

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Site Director at Churchville Elementary

KinderCare Education

Southampton, PA 18966

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Director, Quality (GCP/GCLP/GVP)

LARIMAR THERAPEUTICS

Philadelphia, PA 19102

OnsitePaid Time OffRetirement Benefit

Bachelor's degree in life sciences
A minimum of 10+ years experience in a Quality role supporting Clinical Operations and/or Pharmacovigilance departments within a biotechnology or pharmaceutical environment
Experience managing GCP/GCLP/GVP quality processes, including risk management activities
Demonstrated experience managing GCP inspections, including preparation and response activities
Minimum of 3 years experience performing GCP/GCLP/GVP audits or comparable GxP audit experience
Expert knowledge of GxP systems, quality principles, and GCP/GCLP/GVP regulations (FDA, MHRA, EMA, etc.) and guidance documents (GCP/ICH) and ability to translate understanding to practice
Demonstrated ability to initiate process improvements and take initiative
Must possess a strong attention to detail while having the ability to work independently and collaboratively, as required, in a fast-paced environment

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New, Posted 1 day ago

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Daycare Center Director

The Learning Experience

Hillsborough, NJ 08844

~ 24 min OnsiteChildcare AssistanceEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

State-specific guidelines
Required certifications for the role
To be a childcare center director in New Jersey, you need a bachelor's degree, a Child Development Associate (CDA) credential, or a degree in early childhood education, plus at least three years of experience teaching in early childhood education and one year in a leadership role
Pass a comprehensive criminal background check
Complete required health and safety training
The facility must also pass state licensing inspections
Maintain proper records
A minimum or 12 ECE credits are also required
Possess the state-specific Administrative or Director credential, as well as any other state-specific guidelines for the role
Hold a Bachelor's degree in Early Childhood Education (ECE) or a related field
Demonstrate strong knowledge of state licensing rules and regulations

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Assistant Director of Environmental Services

ARAMARK

Philadelphia, PA 19104

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Staff Product Development Engineer

1010 Analog Devices

Somerset, NJ 08875

New, Posted 1 day ago

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Center Director

The Learning Experience

Lawrenceville, NJ 08648

OnsiteHealth InsurancePaid Time OffRetirement Benefit

Must have a Bachelor's in Early Childhood Education / Education
Two or more years of center leadership/management experience is highly preferred. At least one year of center leadership/management experience required.
Must have professional teaching experience with infants to preschool children.
Strong knowledge of state licensing rules and regulations
Must meet state-specific guidelines

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