How much do Science & Research jobs in Florham Park, NJ pay?

Based on 71 listings with disclosed salaries, most science & research jobs in Florham Park, NJ pay between $101k–$346k per year. Individual offers vary with seniority, company size, and specialization.

How many Science & Research jobs are open in Florham Park, NJ right now?

There are currently 77 open science & research positions in Florham Park, NJ listed on Clera. New openings are added daily as companies post roles.

Which companies are hiring for Science & Research roles in Florham Park, NJ?

Companies currently hiring include Allergan, Shionogi Inc. (U.S.), CACI International Inc, Summit Health, Celularity Inc., among others. Browse the listings above to see every active employer.

Are there remote or hybrid Science & Research jobs in Florham Park, NJ?

Yes — 26 of the 77 open science & research positions offer remote or hybrid work (0 remote, 26 hybrid).

How do I apply for Science & Research jobs in Florham Park, NJ?

Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.

Science & Research Jobs in Florham Park, NJ (Now Hiring) — 77 open — Page 2

Shionogi Inc. (U.S.)

Senior Manager / Associate Director, Regulatory Affairs CMC

Florham Park, New Jersey, United States · Hybrid

$140k–$200k/yr

Senior$383M raised

Overview The Senior Manager/Associate Director, Regulatory Affairs CMC is a strategic and hands on regulatory contributor responsible for defining and executing global CMC regulatory strategies for assigned investigation…

Skills: CMC Regulatory Strategy, Scientific Writing, CTD Authoring, Health Authority Liaison, Change Control

Shionogi Inc. (U.S.)

Manager, Government Operations

Florham Park, New Jersey, United States · Hybrid

$130k–$160k/yr

Senior$383M raised

Overview The Manager, Government Operations will report to the Senior Director, Government Operations and will support program management activities related to Shionogi’s US Government Contracts, including partnerships w…

Skills: Program Management, Government Operations, Contract Management, Federal Compliance, Budgeting

Allergan

Modeling and Simulation Module Developer - Data & AI Acceleration (Hybrid)

Florham Park, New Jersey, United States · Hybrid

$97k–$184k/yr

Mid level

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a r…

Skills: R Programming, Interactive Dashboards, Agentic AI Development, Retrieval-Augmented Generation, Statistical Analysis

Allergan

Senior Medical Director, Hematology Clinical Development

Florham Park, New Jersey, United States · On-site

$182k–$346k/yr

Senior

Skills: Clinical Trial Design, Clinical Development Planning, Regulatory Compliance, Pharmacovigilance, Good Clinical Practices

Allergan

Director, HEOR Strategy (Dermatology)

Florham Park, New Jersey, United States · On-site

$161k–$305k/yr

Senior

Skills: HEOR Strategy, Clinical Research, Cross-functional Leadership, Health Economics, Outcomes Research

Allergan

Senior Director, HEOR Strategy - Neuroscience

Florham Park, New Jersey, United States · On-site

$207k–$393k/yr

Senior+

Skills: HEOR Strategy, Clinical Development, People Leadership, Strategic Planning, Budget Management

Shionogi Inc. (U.S.)

Medical Director, Medical Affairs, ALS

Florham Park, New Jersey, United States · Hybrid

$230k–$280k/yr

Senior+$383M raised

Overview The Medical Director will be responsible for developing and overseeing the execution of Medical Affairs programs in the US that support pre-approval, marketed, and late development products and compounds with a …

Skills: Medical Affairs Strategy, Rare Disease Expertise, KOL Relationship Management, Clinical Development, Scientific Communications

Tutor Doctor of Morris County

STEM Learning Specialist – Professional Sports Academy

Florham Park, New Jersey, United States · On-site

Mid level

High School Mathematics & Science | Two Full Days Per Week Technology delivers the curriculum. Great educators bring it to life. This is an education position inside an elite soccer academy. You do not need to know socce…

Skills: Advanced Mathematics, Calculus, Pre-Calculus, Algebra II, Geometry

Triumvirate Environmental

Air Monitoring Technician

Florham Park, New Jersey, United States · On-site

Entry level

Air Monitoring Technician Triumvirate Environmental, one of the largest environmental services firms in North America, is seeking an Air Monitoring Technician for our Florham Park, NJ team. You will provide onsite operat…

Skills: Air Monitoring, Environmental Sampling

Allergan

Data Strategy Lead - Hybrid

Florham Park, New Jersey, United States · Hybrid

$110k–$209k/yr

Senior

Skills: Clinical Data Strategy, Project Management, Clinical Trial Technology, Data Management, Cross-functional Collaboration

Allergan

Director of RA CMC Knowledge Management & Strategy

Florham Park, New Jersey, United States · On-site

$182k–$346k/yr

Senior+

Skills: Regulatory Affairs, Drug Development, CMC Experience, Global CMC Regulatory Requirements, Influencing Skills

Summit Health

Specialty Oncology Pharmacist

Florham Park, New Jersey, United States · Hybrid

Mid level

About Our Company We’re a physician-led, patient-centric network committed to simplifying health care and bringing a more connected kind of care. Our primary, multispecialty, and urgent care providers serve millions of p…

Skills: Medication Therapy Management, Clinical Pharmacy, Patient Education, Pharmacotherapy, Collaborative Practice Agreements

Allergan

Study Project Manager, II - Hybrid

Florham Park, New Jersey, United States · Hybrid

$125k–$237k/yr

Senior

Skills: Clinical Study Operations, Stakeholder Management, Risk Management, Vendor Management, Budget Oversight

Allergan

Senior Scientific Director, Oncology Clinical Development (Non-Hodgkin Lymphoma)

Florham Park, New Jersey, United States · On-site

$207k–$393k/yr

Senior+

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable imp…

Skills: Clinical Trial Design, Clinical Development Planning, Regulatory Compliance, Cross-functional Leadership, Hematology

Allergan

TA Director, Risk Management Lead - Multiple Therapeutic Areas (Hybrid)

Florham Park, New Jersey, United States · Hybrid

$161k–$305k/yr

Senior+

Skills: Risk Management, Clinical Research, Clinical Operations, Risk-Based Quality Management, People Management

Summit Health

Ultrasound Tech - Imaging Department

Florham Park, New Jersey, United States · On-site

$42/hr–$52/hr

Mid level

Skills: Ultrasound Imaging, Patient Care, Diagnostic Imaging, Infection Control, Patient History Documentation

CACI

Embedded Software Engineer - Photonics

Florham Park, New Jersey, United States · On-site

$94k–$198k/yr

Mid level

Job Title: Embedded Software Engineer - Photonics Job Category: Engineering Time Type: Full time Minimum Clearance Required to Start: None Employee Type: Regular Percentage of Travel Required: Up to 10% Type of Travel: C…

Skills: C/C++, Embedded Computing, RTOS, Python, ARM Processors

CACI International Inc

Embedded Software Engineer - Photonics

Florham Park, New Jersey, United States · On-site

$94k–$198k/yr

Mid level$1.5B raised

Skills: C/C++, Embedded Computing, RTOS, Python, ARM Processors

Allergan

Head of Asset in GU, Oncology Clinical Development

Florham Park, New Jersey, United States · On-site

$248k–$472k/yr

Senior+

Skills: Clinical Trial Design, Clinical Development Planning, Regulatory Compliance, People Management, Cross-functional Leadership

Allergan

Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline (Prostate Cancer)

Florham Park, New Jersey, United States · Hybrid

$182k–$346k/yr

Senior+

Skills: Medical Affairs Strategy, Clinical Trial Methodology, Evidence Generation, Prostate Cancer Expertise, Cross-functional Leadership

Overview

The Senior Manager/Associate Director, Regulatory Affairs CMC is a strategic and hands on regulatory contributor responsible for defining and executing global CMC regulatory strategies for assigned investigational and/or marketed assets. The role partners closely with technical, quality, supply and program teams to communicate regulatory strategies and deliver scientifically sound, submission ready CMC content using a risk based approach. This individual demonstrates exceptional scientific writing, precision, and attention to detail, applies creative thinking and a collaborative, high quality approach that ensures data integrity, regulatory compliance, and trust with cross functional partners and health authorities.

Responsibilities

Lead development of Global CMC regulatory strategies across the product lifecycle.
Define, prioritize, and execute multiple CMC regulatory activities, recognizing when to escalate decisions, risks, or strategic inflection points to management to ensure alignment and avoid placing CMC on the critical path for approvals.
Track, manage, and coordinate multiple CMC regulatory project timelines, aligning ongoing activities across cross‑functional teams to ensure timely delivery of submission documentation.
Review and approve change control documentation, providing clear regulatory expectations, feedback on supporting data, and guidance on appropriate regulatory pathways or strategies.
Provide regulatory assessment and strategic guidance on CMC documentation for regulatory submissions, including evaluation of development plans, control strategies, labeling content, and Health Authority responses. Ensure submissions are complete, consistent, and aligned with Health Authority expectations, while effectively navigating regulatory ambiguity.
Author, review, and maintain CMC CTD sections across the product lifecycle, including INDs/IMPDs, NDAs/MAAs/NDSs, and DMF/ASMF/MF submissions, amendments, supplements, variations, and annual reports, ensuring high‑quality, consistent, submission‑ready content delivered in accordance with established timelines.
Serve as the primary CMC regulatory liaison with Health Authorities for designated assets, which involves guiding agency communications, creating briefing documents, handling information requests, and ensuring alignment with management on strategic or high‑risk issues before making commitments.
Builds trusted relationships and influences internal and external stakeholders across global cross-functional teams, including supply chain, manufacturing sites, CMC technical, QA, and CMOs.
Maintain expertise in emerging and evolving CMC regulatory requirements and proactively deliver training and regulatory guidance to Regulatory, Manufacturing and Quality groups on applicable topics.
Able to incorporate AI‑driven tools into CMC regulatory activities, ensuring traceability, and independent verification of information.
Function as a regulatory CMC technical expert for cross-functional teams.
Resolve importation and customs matters for assigned assets, supporting product supply and operational continuity.
Provide support for labeling activities.
Manage and/or support Establishment Registrations, Drug Listings and CARES Act reporting.
Other duties as assigned.

Minimum Job Requirements

Qualifications

Bachelor’s degree in a scientific discipline. Advanced degree preferred. RAC a plus though not required.
A minimum of 5 years (Senior Manager) or 7+ years (Associate Director) of Regulatory Affairs CMC experience in a strategic and operational role.
In-depth knowledge of global CMC regulatory requirements across the product lifecycle (development, registration, and post-approval).
Proven hands-on experience with global regulatory submissions (e.g., INDs/CTAs, NDAs/BLAs/MAAs) and accountability for post‑approval lifecycle management submissions.
Demonstrated ability to effectively communicate, influence, and negotiate CMC regulatory strategies while building alignment across management and cross-functional teams.
Prior experience interfacing with Health Authorities on CMC-related topics.
Proficiency with regulatory systems (e.g., Veeva Vault, eCTD, etc.).

Competencies

In‑depth knowledge of global regulatory CMC requirements for advanced therapies and/or biologics across the product lifecycle, including development, registration, and post‑approval change management.
Solid understanding of the downstream development and commercialization implications of regulatory CMC decisions, enabling risk‑based, phase‑appropriate regulatory strategies.
Strategic and hands on regulatory leader, able to independently develop regulatory CMC approaches and proactively align with regulatory leadership and management obtaining agreement on strategy prior to communication or implementation with cross‑functional teams.
Established record of leading cross‑functional CMC teams, coordinating complex activities within a matrixed environment, and exercising full ownership for the writing, quality, and delivery of regulatory CMC submissions, and responses to Health Authorities.
Demonstrated success engaging with Health Authorities on CMC-related topics.
Advanced scientific writing skills, with a strong focus on compliance, quality, and data integrity, ensuring the regulatory CMC submissions align with global regulatory requirements.
Excellent verbal communication skills, with demonstrated ability to act as a regulatory CMC spokesperson and effectively communicate aligned regulatory CMC strategies and positions across working teams, cross‑functional forums, and senior leadership.
Proven capability to assess regulatory risk and make informed decisions independently, with clear judgment on when to escalate complex or high‑risk CMC issues.
Ability to mentor and develop others.
High level of proficiency in Microsoft Office (Word, Excel, PowerPoint), enabling development of high‑quality regulatory documents, data summaries, and executive‑level presentations with minimal supervision.

Other Requirements

Ability and willingness to travel approximately 10% of the year both domestically and internationally
Must live a commutable distance to our US Corporate Headquarters in Florham Park, NJ. Office presence required at least 50% of the time per month.

Additional Information

The base salary range for this full-time position is $140,000 - $200,000. Individual pay is determined by several factors, which include but are not limited to: job-related skills, experience, and relevant education or training. The range does not include the comprehensive benefits, bonus, long-term incentive, applicable allowances, or any additional compensation that may be associated with this role.

EEO

Shionogi Inc. is an equal opportunity employer supporting individuals with disabilities and veterans. All qualified applicants will receive equal consideration for employment opportunities based on valid job requirements without regard to race, color, religion, sex (including pregnancy), marital status, national origin, age, ancestry, citizenship, disability, genetic information, status as a disabled veteran, a recently separated veteran, Active Duty Wartime or Campaign Badge Veterans, and Armed Forces Service Medal Veterans, or any other characteristic protected by applicable law. It is the policy of Shionogi Inc. to undertake affirmative action for protected veterans and individuals with disabilities in compliance with all federal, state, and local requirements to recruit a diverse pool of protected veteran and individuals with disabilities applicants and to ensure that our employment practices are, in fact, non-discriminatory.

If you are qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request accommodations by calling 973-307-3550 or by sending an email to [email protected].

Science & Research Jobs in Florham Park, NJ (Now Hiring) — 77 open — Page 2

Senior Manager / Associate Director, Regulatory Affairs CMC

Manager, Government Operations

Modeling and Simulation Module Developer - Data & AI Acceleration (Hybrid)

Senior Medical Director, Hematology Clinical Development

Director, HEOR Strategy (Dermatology)

Senior Director, HEOR Strategy - Neuroscience

Medical Director, Medical Affairs, ALS

STEM Learning Specialist – Professional Sports Academy

Air Monitoring Technician

Data Strategy Lead - Hybrid

Director of RA CMC Knowledge Management & Strategy

Specialty Oncology Pharmacist

Study Project Manager, II - Hybrid

Senior Scientific Director, Oncology Clinical Development (Non-Hodgkin Lymphoma)

TA Director, Risk Management Lead - Multiple Therapeutic Areas (Hybrid)

Ultrasound Tech - Imaging Department

Embedded Software Engineer - Photonics

Embedded Software Engineer - Photonics

Head of Asset in GU, Oncology Clinical Development

Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline (Prostate Cancer)

Senior Manager / Associate Director, Regulatory Affairs CMC

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How much do Science & Research jobs in Florham Park, NJ pay?

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Which companies are hiring for Science & Research roles in Florham Park, NJ?

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How do I apply for Science & Research jobs in Florham Park, NJ?

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