This position requires a hybrid working model, with expectations of being in office 2-3 days a week at an office in Princeton, New Jersey (preferred location). Company Overview: SystImmune Inc. is a dynamic clinical-stag…
Manager, Analytical AI Forecasting and Predictive Solutions
Princeton, New Jersey, United States · Hybrid
$96k–$116k/yr
Mid level$29B raised
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every …
This position requires a hybrid working model, with expectations of being in office 2-3 days a week at an office in Princeton, New Jersey (preferred location) or Redmond, Washington. Company Overview: SystImmune Inc. is …
This position requires a hybrid working model, with expectations of being in office 2-3 days a week at an office in Princeton, New Jersey (preferred location) or Redmond, Washington. Company Overview: SystImmune Inc. is …
Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology. Here at As…
Skills: Human resources business partner, Organizational effectiveness, Workforce planning, Leadership development, Talent management
Dr. Reddy's Laboratories
Group Lead Intellectual Property Counsel
Princeton, New Jersey, United States · Hybrid
Senior+$6M raised
Company Description At Dr Reddy's "Good Health Can't Wait" By joining Dr Reddy’s, you will contribute to making the breakthroughs of tomorrow a reality today! From making medicines more affordable to discovering innovati…
Director / Lead Pricing and Contracting - Biologics
Princeton, New Jersey, United States · On-site
Senior$6M raised
Company Description At Dr. Reddy's "Good Health Can't Wait" By joining Dr. Reddy’s, you will contribute to making the breakthroughs of tomorrow a reality today! From making medicines more affordable to discovering innova…
Skills: Pricing Strategy, Contracting, Gross To Net Modeling, Financial Analysis, ASP Forecasting
ABOUT VEG In 2014, VEG was born with a mission to help people and their pets when they need it most. This meant challenging the status quo and fixing everything that was wrong with the ER experience. Since then, we’ve ex…
ABOUT VEG In 2014, VEG was born with a mission to help people and their pets when they need it most. This meant challenging the status quo and fixing everything that was wrong with the ER experience. Since then, we’ve ex…
Company Description At Dr Reddy's "Good Health Can't Wait" By joining Dr Reddy’s, you will contribute to making the breakthroughs of tomorrow a reality today! From making medicines more affordable to discovering innovati…
Skills: Patent Litigation, Hatch-Waxman Matters, IP Strategy, ANDA/ANDS, 505(b)(2)
Dr. Reddy's Laboratories
Director / Lead Intellectual Property Counsel
Princeton, New Jersey, United States · Hybrid
Senior+$6M raised
Company Description At Dr Reddy's "Good Health Can't Wait" By joining Dr Reddy’s, you will contribute to making the breakthroughs of tomorrow a reality today! From making medicines more affordable to discovering innovati…
Overview Marquand Library seeks to hire a Library Collections Specialist, Level VI (LCS VI). The Marquand Library of Art and Archaeology is one of the oldest and most extensive art libraries in America. The collection of…
Skills: Metadata creation, Digital library management, Rare book handling, Cataloging, Preservation techniques
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every …
Associate Director, Global Medical Cardiovascular, Mavacamten
Princeton, New Jersey, United States · Hybrid
$166k–$202k/yr
Senior$29B raised
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every …
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every …
Skills: Clinical pharmacology, Pharmacokinetics, Pharmacodynamics, Model informed drug development, NONMEM
The Role Moderna is seeking a Counsel, Market Access and Commercial Operations to take responsibility for providing legal support for the commercialization of the Moderna COVID-19 Vaccine in the U.S. and, over time, othe…
South San Francisco, California, United States · Hybrid
$194k–$250k/yr
Senior+$554M raised
About Us Kardigan is a heart health company working to make cardiovascular disease preventable, curable and no longer the leading cause of death in the world. It is Kardigan’s mission to develop multiple targeted treatme…
Director, GCP Inspection Readiness and Audits Strategy
South San Francisco, California, United States · Hybrid
$194k–$250k/yr
Senior+$554M raised
About Us Kardigan is a heart health company working to make cardiovascular disease preventable, curable and no longer the leading cause of death in the world. It is Kardigan’s mission to develop multiple targeted treatme…
Senior Medical Director/Medical Director, Clinical Trial Lead
South San Francisco, California, United States · Hybrid
$242k–$347k/yr
Senior+$554M raised
About Us Kardigan is a heart health company working to make cardiovascular disease preventable, curable and no longer the leading cause of death in the world. It is Kardigan’s mission to develop multiple targeted treatme…
Skills: Clinical Development, Medical Monitoring, Protocol Design, Regulatory Submissions, Cardiology
Sr. Director, Medical Science Liaison / Regional Medical Lead - Northeast Region
South San Francisco, California, United States · On-site
$220k–$320k/yr
Senior$554M raised
About Us Kardigan is a heart health company working to make cardiovascular disease preventable, curable and no longer the leading cause of death in the world. It is Kardigan’s mission to develop multiple targeted treatme…
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$150k–$190k/yr
Full-time
bachelor degree
Medical insurance, Dental insurance, Vision insurance, Short-term disability, Long-term disability, 401(k) plan
Posted 7d ago
Apply by Nov 16
~40 hrs/week
Responsibilities
The Associate Director provides strategic leadership and oversight of Clinical Quality programs to ensure compliance with global GCP and GVP regulations. They manage audit programs, lead inspection readiness activities, and oversee quality systems and vendor performance.
Requirements
Candidates must have a Bachelor’s degree in Life Sciences or a related field and at least 8 years of experience in Clinical Quality Assurance or clinical research. A minimum of 5 years of direct GCP Quality Assurance experience is required, with preference for oncology clinical development background.
Full job description
This position requires a hybrid working model, with expectations of being in office 2-3 days a week at an office in Princeton, New Jersey (preferred location).
Company Overview:
SystImmune Inc. is a dynamic clinical-stage bio-pharmaceutical company headquartered in Redmond, WA. Our mission is to revolutionize cancer treatment by developing breakthrough-therapeutic multi-specific antibodies and ADCs. With eight assets in ongoing clinical trials and a robust preclinical pipeline, we are committed to advancing innovative therapies from discovery through IND-enabling stages.
Job Summary:
The Associate Director, Clinical Quality Assurance (GCP/GVP) is responsible for providing strategic leadership and oversight of Clinical Quality programs to ensure compliance with global Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GVP) regulations, guidelines, and company standards.
This position partners closely with Clinical Operations, Drug Safety/Pharmacovigilance, Regulatory Affairs, Biometrics, and external vendors to ensure the effective implementation of quality systems, proactive risk management, inspection readiness, and continuous improvement initiatives. The Associate Director serves as a key quality advisor across development programs and contributes to the advancement of a culture of quality and compliance throughout the organization.
Quality Systems & Compliance
Provide oversight and guidance to ensure compliance with global GCP and GVP regulations, including FDA, EMA, MHRA, PMDA, NMPA, and ICH requirements.
Support the development, implementation, and continuous improvement of the Clinical Quality Management System (QMS).
Lead quality risk management activities, including quality risk assessments and mitigation planning.
Ensure quality processes remain aligned with evolving regulatory expectations and industry best practices.
Audit Program Management
Develop and execute risk-based annual GCP/GVP audit programs.
Lead and/or oversee internal, external, investigator site, vendor, CRO, and pharmacovigilance audits.
Review audit findings, assess systemic impact, and ensure appropriate remediation activities are implemented.
Identify compliance trends and recommend strategic quality improvements.
Inspection Readiness
Lead inspection readiness activities across clinical development and pharmacovigilance functions.
Support regulatory agency inspections and sponsor audits.
Coordinate inspection preparation activities, including mock inspections and readiness assessments
Provide strategic guidance during regulatory inspections and ensure effective management of inspection responses.
Facilitate root cause analysis and ensure CAPAs are appropriately developed, implemented, and verified for effectiveness.
Monitor quality events and CAPA metrics to identify trends and opportunities for improvement. Vendor Quality Oversight
Lead quality oversight activities for CROs, pharmacovigilance vendors, laboratories, technology providers, and other GCP/GVP service providers.
Support vendor qualification, risk assessments, audits, and ongoing performance monitoring.
Provide quality input during vendor selection and governance activities.
Ensure outsourced activities maintain appropriate regulatory compliance and quality standards.
Quality Metrics & Risk-Based Quality Management
Establish and monitor key quality metrics and compliance indicators.
Analyze quality data to identify emerging risks, compliance trends, and systemic improvement opportunities.
Support implementation of Risk-Based Quality Management (RBQM) strategies and Quality Tolerance Limits (QTLs).
Present quality metrics and compliance status to senior leadership.
SOP Development & Training
Lead development, review, and lifecycle management of GCP, GVP, and Clinical Quality SOPs and associated procedures.
Develop and deliver quality training programs.
Provide quality consultation and mentoring to cross-functional teams.
Promote a culture of quality, inspection readiness, and continuous improvement.
Leadership & Strategic Partnership
Serve as a trusted quality advisor to clinical development teams.
Lead cross-functional quality initiatives supporting organizational objectives.
Mentor junior quality professionals and support development of departmental capabilities.
Contribute to long-term Clinical Quality strategy, resource planning, and operational excellence initiatives.
Qualifications/Requirements:
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field required.
8+ years of experience in Clinical Quality Assurance, Clinical Research, Pharmacovigilance, or related pharmaceutical/biotechnology functions.
Minimum 5 years of direct GCP Quality Assurance experience.
Demonstrated experience leading GCP audits, vendor audits, and inspection readiness programs.
Experience supporting regulatory authority inspections (FDA, EMA, MHRA, PMDA, NMPA, or equivalent).
Experience within oncology clinical development strongly preferred.
Experience working in global clinical development environments and managing outsourced service providers.
Benefits:
Competitive salary and benefits package.
Opportunities for professional development and career advancement.
Work in a dynamic and collaborative environment at the forefront of clinical research.
Contribute to meaningful projects that have the potential to improve patient outcomes and advance medical science.
The hiring pay range for this position is $150,000 - $190,000 per year based on skills, education, and experience relevant to the role.
SystImmune is a stable, well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
Located in Redmond WA, founded in 2014, Systimmune Inc. is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic bi-specific, and tri-specific antibodies, as well as antibody-drug conjugates (ADC's). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor. We are a group of highly experienced immuno-oncology scientists utilizing several technology platforms to develop world class advanced antibody-based drug therapies.
Offices: 22213 30th Drive SE, Bothell, WA 98021, US · 15318 NE 95th St, Redmond, Washington, US
Health CareBiopharmaProfessional ServicesBiotechnologyTherapeutics
How much do Science & Research jobs in Princeton, NJ pay?
Based on 306 listings with disclosed salaries, most science & research jobs in Princeton, NJ pay between $95k–$244k per year. Individual offers vary with seniority, company size, and specialization.
How many Science & Research jobs are open in Princeton, NJ right now?
There are currently 338 open science & research positions in Princeton, NJ listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Princeton, NJ?
Companies currently hiring include Bristol Myers Squibb, Kardigan, Otsuka Pharmaceutical Companies (U.S.), dsm-firmenich, Princeton University Strategic Partnerships and Engagement, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Princeton, NJ?
Yes — 192 of the 338 open science & research positions offer remote or hybrid work (29 remote, 163 hybrid).
How do I apply for Science & Research jobs in Princeton, 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.