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Our specialized experience includes design for energy, manufacturing and industrial process, data centers, healthcare, science and technology, high-rise buildings, education, and other building types as well as structural and building sciences, infrastructure asset management, advanced robotics, and more. Our technical expertise is paired with an exceptional team of business development, human resources, finance and accounting, information technology, and marketing professionals, all of whom play a key role in delivering outstanding customer service and building long-term careers.

Salas O'Brien

Senior Building Consultant, North East

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Also, we are unable to accept substance abuse counselors, school counselors, registered nurses, career counselors, Christian counselors, and business coaches (unless they have an additional license as a mental health counselor). BetterHelp is one of the world’s largest online therapy platforms for mental health professionals who want to focus on client care — not admin or overhead.

BetterHelp is the largest online counseling platform worldwide. We change the way people get help with facing life's challenges by providing convenient, discreet and affordable access to a licensed therapist. BetterHelp makes professional counseling available anytime, anywhere, through a computer, tablet or smartphone.

BetterHelp

Licensed Marriage and Family Therapist

Reporting to the Executive Director, Head of Programming, you’ll provide technical leadership as the Program Lead for an assigned compound and ensure adequate programming support for the studies of that compound as well as successful implementation of programming strategies and efficient execution of analyses. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress.

Insmed

Associate Director, Programming

The ideal candidate will design, develop, optimize, and maintain SQL Server databases, ETL processes, and data integration solutions. Job Summary: Seeking an experienced SQL Developer with strong expertise in T-SQL, SSIS, and ETL development.

Two95 International Inc.

SQL Developer (T-Sql / Ssis / Etl)

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Incident Response: Coordinate the incident response process, including conducting root cause analysis, identifying remediation actions, and implementing changes to prevent similar incidents. Risk Management: Identify, assess, and mitigate technology risks to ensure the security, reliability, and availability of technology systems and services.

Globalchannelmanagement

Remote IT Incident Analyst

Through our expert-led training, they will have the opportunity to develop specialization in women’s mental health across hormonally influenced life transitions, including fertility, pregnancy, postpartum, parenting, PMDD, and perimenopause/menopause, with a focus on supporting patients through the complex intersection of biology, identity, and lived experience. Now a WPS Healthcare Company , Mavida Health combines the best of both worlds: the speed, autonomy, and impact of a high-growth startup with the resources and reach of a legacy healthcare organization.

Mavida Health

Psychiatric Mental Health Nurse Practitioner (PMHNP) - NJ (Full-Time)

Reporting to the Senior Director, Regulatory Affairs CMC, EMEA, you’ll have responsibility for leading CMC regulatory strategy development and implementation that incorporates risk identification and mitigation for assigned development and post approval programs to achieve regulatory approvals in the EMEA region. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress.

Associate Director, Regulatory Affairs (CMC)

Maxion Research invites people in Trenton, NJ to join an online research panel and be considered for optional surveys, interviews, focus groups, and product-feedback studies. Research activities may include completing online questionnaires, joining remote discussions, testing concepts, or sharing opinions about products and services.

Maxion Corp

Online Research Panel Participant - Trenton, NJ

You’ll have responsibility for the management of API/Intermediate/RSM manufacturing at Insmed’s CMOs including synthesis route and early-stage process identification, tech transfer, process optimization, clinical/commercial manufacturing, process characterization and validation, and manufacturing CMC development strategy. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress.

Director, Process Chemistry

Provide proactive legal advice to business partners and drive legal strategy through the review of brand team initiatives in support of execution of brand plan for one of Insmed’s marketed respiratory products in accordance with current FDA and FTC regulations, guidance, and enforcement activities with a focus on anti-kickback, false claims act, and advertising and promotional regulations, and counsel on risk mitigation strategies, as needed. Identify, communicate, and provide updates to business partners and the legal team on risks associated with day-to-day operational business activities and on current federal and state legal, regulatory, and enforcement developments related to the life sciences industry, including training clients on applicable legal issues within your expertise.

Director, Brand Counsel

Reporting to the Director, Technical Operations - Project Management, you’ll be a critical contributor within Insmed’s Technical Operations Department, responsible for driving complex pipeline projects from research transition through development, registration, and commercial readiness. This role leads cross-functional Chemistry, Manufacturing & Controls (CMC) teams and collaborates with internal departments and external partners to ensure timely, high-quality project delivery.

Manager, Project Management – Technical Operations

As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress. Provide strategic leadership for API development, API process development, technology transfer, process validation, manufacturing readiness, and lifecycle management across development programs.

Executive Director, API Development, Small Molecule

Reporting to the Executive Director, DSPV Medical Safety, you’ll oversee a team of Pharmacovigilance (PV) Scientists responsible for signal detection, risk management, aggregate safety reporting, and clinical trial safety support and ensure the delivery of high-quality safety surveillance activities throughout the product lifecycle while maintaining compliance with global pharmacovigilance regulations and company procedures. You have a Master's degree or PhD in Pharmacy, Pharmacology, Life Sciences, Nursing, Public Health, or a related scientific discipline along with 10 years of experience in within the pharma/biotech industry as well as minimum of 5 years of direct people management experience leading PV Scientists or Medical Safety professionals.

Director, Medical Safety

Analyze supplier quality data and performance trends, including deviations, CAPAs, audit findings, inspection outcomes, data integrity issues, and timeliness metrics, and facilitate, in collaboration with functional representative supplier governance forums and business reviews to drive remediation actions, corrective measures, and continuous improvement while maintaining accurate supplier records and approved supplier listings. Partner with DevQA to develop, manage, and continuously improve supplier performance monitoring frameworks for clinical suppliers in collaboration with the functional representatives, including KPIs, scorecards, and quality metrics, ensuring accurate risk-based scoring, timely completion, and appropriate control alignment.

Senior Manager, Clinical Supplier Quality

Author, review and provide input and approval for drug-safety related regulatory reports and clinical study documents including clinical study protocols, Informed Consent Forms, Investigator Brochures, Integrated Summary of Safety (ISS), Integrated Summary of Efficacy (ISE), MedDRA coding of AEs, product package and labeling. Investigate and review emerging safety data from various sources including individual clinical trial AE/SAE case reports, spontaneous Adverse Drug Reaction (ADR) reports, published literature, aggregate reports, toxicology reports, non-clinical studies, and other source.

Associate Director, Pharmacovigilance/Product Safety

We are industry leaders in video security and analytics, with solutions deployed in more than 120 countries across diverse environments such as school campuses, transportation systems, healthcare centers, public venues, critical infrastructure, prisons, factories, casinos, airports, financial institutions, government facilities, and retailers. Organizational Leadership and Talent Strategy: Manage and scale a unified computer vision research and engineering organization distributed across multiple geographies, overseeing multiple teams, and defining the strategy for recruiting, mentoring, and attracting world-class talent.

YEAR

Motorola Solutions Inc

Director of Computer Vision

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Enable Medical Affairs Teams with data, tools, and models to inform prioritization of activity and planning (i.e. channel engagement, ME identification and segmentation, etc ) Drive ad-hoc analyses to support Medical Affairs strategic understanding to enable launch preparation and success. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress.

Director Medical Insights & Analytics

Maxion Research invites people in Toms River, NJ to join an online research panel and be considered for optional surveys, interviews, focus groups, and product-feedback studies. Research activities may include completing online questionnaires, joining remote discussions, testing concepts, or sharing opinions about products and services.

Online Research Panel Participant - Toms River, NJ

You’ll join a values‑driven community where integrity guides decisions, relentless service sets the bar, and we thrive on big challenges together. Builds trust and alignment through open communication, shared goals, and strong partnerships to drive collective success.

Epiq

Principal Consultant

OTHER

Through our comprehensive suite of innovative supplemental benefits, fintech payment platforms, and member engagement solutions, we help health plans deliver high-quality benefits to their members that address the social determinants of health and improve member health outcomes and satisfaction. Work closely with clinic teams to support patient flow and ensure efficient appointments Act as a clinical resource for providers and staff needing audiology expertise.

Work From Home Jobs in Toms River, NJ

Senior Building Consultant, North East Salas O'Brien

Licensed Marriage and Family Therapist BetterHelp

Associate Director, Programming Insmed

SQL Developer (T-Sql / Ssis / Etl) Two95 International Inc.

Remote IT Incident Analyst Globalchannelmanagement

Psychiatric Mental Health Nurse Practitioner (PMHNP) - NJ (Full-Time) Mavida Health

Associate Director, Regulatory Affairs (CMC) Insmed

Online Research Panel Participant - Trenton, NJ Maxion Corp

Director, Process Chemistry Insmed

Director, Brand Counsel Insmed

Manager, Project Management – Technical Operations Insmed

Executive Director, API Development, Small Molecule Insmed

Director, Medical Safety Insmed

Senior Manager, Clinical Supplier Quality Insmed

Associate Director, Pharmacovigilance/Product Safety Insmed

Director of Computer Vision Motorola Solutions Inc

Director Medical Insights & Analytics Insmed

Online Research Panel Participant - Toms River, NJ Maxion Corp

Principal Consultant Epiq

Teleaudiologist NationsBenefits, LLC

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