Cambridge, Massachusetts, United States · Hybrid
$159k–$286k/yr
The Role: This role will support Oncology Therapeutic programs, specifically supporting the Clinical Development Lead in the direction, execution and evaluation of Phase 1-3 clinical studies. The principal responsibility…
Skills: Clinical Study Design, Oncology Knowledge, Clinical Data Review, Regulatory Submissions, Medical Safety Monitoring
Princeton, New Jersey, United States · On-site
$150k–$224k/yr
Job Description The Associate Director, R&D Strategic Sourcing, will lead strategic sourcing efforts for key R&D categories. This role plays a critical part in enabling innovation by securing high-performing suppliers an…
Skills: Strategic Sourcing, Category Management, Contract Negotiation, Supplier Relationship Management, Spend Analysis
Clifton, New Jersey, United States · On-site
$31/hr–$42/hr
It's fun to work in a company where people truly BELIEVE in what they're doing! We're committed to bringing passion and customer focus to the business. SummaryThe Radiologic Technologist (X-ray Tech) is responsible for a…
Skills: Radiologic Technology, Pediatric Care, Digital Imaging, Electronic Health Records, Patient Intake
Hackensack, New Jersey, United States · On-site
Overview Our team members are the heart of what makes us better. At Hackensack Meridian Health we help our patients live better, healthier lives — and we help one another to succeed. With a culture rooted in connection a…
Skills: Medical Genetics Consultation, Genetic Counseling, Case Management, Patient Education, Clinical Research
Montclair, New Jersey, United States · On-site
$40/hr–$50/hr
Teacher Tutors is hiring a part-time Chemistry Tutor to join our team on a flexible basis. This role is ideal for tutors with strong chemistry backgrounds who want to work one-on-one with motivated and struggling student…
Skills: Chemistry Tutoring, Organic Chemistry, General Chemistry, AP Chemistry, Stoichiometry
Egg Harbor Township, New Jersey, United States · On-site
Description B Positive is a blood plasma donation facility seeking an experienced LPN/Paramedic to join our growing team as we expand. Need to have availability Monday - Friday. Competitive Pay PLUS a $3,000 Sign-on Bonu…
Skills: Phlebotomy, Physical Examinations, Medical History Taking, Donor Counseling, CPR
Norwood, New Jersey, United States · On-site
$21/hr–$25/hr
Fragrance Compounder/Blender Location: Norwood, NJ Job Type: Full-Time Schedule: Monday through Friday, 6:00 AM to 2:30 PM Join Our Team! Phoenix Flavors & Fragrances is a leading manufacturer of innovative fragrance and…
Skills: Fragrance Compounding, Flavor Blending, GMP Documentation, Equipment Sanitization, Raw Material Handling
Brick Township, New Jersey, United States · On-site
🚨 IMMEDIATE OPENING – FAST INTERVIEW PROCESS 🚨🫀 Nuclear Medicine Technologist (Cardiac PET/CT) 📍 Brick, Manahawkin, and Keyport NJ | Full-Time | Day Shift 💡 Top-Tier Pay. Stable Schedule. Advanced Cardiac Imag…
Skills: Cardiac PET/CT Imaging, Radiopharmaceutical Administration, Hot Lab Management, Patient Care, ALARA Compliance
Piscataway Township, New Jersey, United States · On-site
$35/hr–$45/hr
The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconduct…
Skills: Raman Spectroscopy, Optical Instrumentation, Technical Troubleshooting, Preventive Maintenance, System Calibration
Pemberton Township, New Jersey, United States · On-site
Position Summary: Under the direction of the Pharmacy Operations Manager, process medication orders resulting in patients receiving safe and effective drug therapy. Provide supervision to Pharmacy Technicians assisting i…
Skills: Medication Order Processing, Pharmacy Technician Supervision, Interpersonal Skills, Computer Skills, Time Management
Piscataway Township, New Jersey, United States · On-site
$85k–$105k/yr
The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconduct…
Skills: Sales Strategy, Prospecting, Product Demonstrations, CRM Management, Technical Presentations
West Deptford Township, New Jersey, United States · On-site
$80k–$95k/yr
Discover Veranova: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance,…
Skills: Process Design, Root Cause Analysis, Scale-up, Process Validation, Batch Manufacturing
Freehold, New Jersey, United States · On-site
$60k–$65k/yr
Description POSITION: Entry level Project Manager / Environmental Technician – Industrial Hygiene POSITION SUMMARY AEI Consultants is currently seeking an energetic and professional Project Manager/Environmental Technici…
Skills: Environmental Consulting, Asbestos Sampling, Mold Sampling, Lead-based Paint Testing, Indoor Air Quality Testing
Morristown, New Jersey, United States · On-site
$94k–$140k/yr
At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where 'Health for all Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curios…
Skills: Formulation Development, Product Prototyping, Gummies Development, VMS Development, cGMP
Hopewell Township, New Jersey, United States · Remote OK
Description Zydus Therapeutics (ZTI) is a clinical stage, specialty-focused bio-pharmaceutical company focused on developing transformative treatments to transform lives, starting with rare and serious liver diseases. Ou…
Skills: Market Access, Account Management, Contract Negotiation, Formulary Coverage, Strategic Planning
Brick Township, New Jersey, United States · On-site
$65/hr–$75/hr
There are a lot of BCBA jobs in New Jersey. Most of them will tell you about their competitive salary, their flexible schedule, and their “supportive team.” We’d rather tell you who we are. At Step Up F…
Skills: Functional Behavior Assessments, Treatment Planning, Clinical Supervision, Caregiver Training, Case Management
Paterson, New Jersey, United States · On-site
Responsible for performing and documenting patient pharmacy clinical interventions, education, and counseling that pertains to medication management and safety. Interprets, evaluates and reviews of physician inpatient or…
Skills: Medication Management, Patient Counseling, Clinical Interventions, Drug Interaction Review, Compounding
Mount Olive, New Jersey, United States · On-site
Overview R&D Expert Electrical Engineer Full Time Hardware Design - Budd Lake, NJ or Loveland, CO Keysight Technologies, the world's largest test and measurement equipment manufacturer, has an outstanding research and de…
Skills: Power Electronics, Switching Converter Design, Analog Design, Control Systems, Digital Signal Processing
Bound Brook, New Jersey, United States · On-site
Company Description SAM is a fast-growing and global sensory and consumer research consultancy. Our mission is to allow consumers a voice in the development of outstanding food, beverage, pet, and health & beauty product…
Skills: Food Preparation, Consumer Testing, Data Collection, Interpersonal Skills, Attention To Detail
Bridgewater Township, New Jersey, United States · Remote OK
$150k–$200k/yr
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, a…
Skills: Statistical Methodology, Clinical Trial Management, Sample Size Estimation, Statistical Analysis Planning, Statistical Modeling
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Oversee the end-to-end delivery of Phase 1-3 oncology clinical trial protocols, including design, execution, and closeout. Ensure comprehensive data quality and integrity to support internal governance and regulatory submissions.
Requires a postgraduate degree (PhD, PharmD, or Masters) and at least 8 years of clinical development experience in a pharmaceutical or biotech company. Must possess significant scientific oncology knowledge and proficiency in clinical data analytics platforms.
This role will support Oncology Therapeutic programs, specifically supporting the Clinical Development Lead in the direction, execution and evaluation of Phase 1-3 clinical studies. The principal responsibility for this role is ensuring the comprehensive data quality of clinical studies to support internal governance decisions and support regulatory submissions.
In conjunction with the Clinical Development Lead and the broader clinical development team, contribute to regulatory and clinical program strategy, clinical trial design and clinical study execution.
Author and review clinical study documents in compliance with regulatory standards, including: clinical protocols, informed consent documents, Development Safety Update Reports (DSUR) and clinical components of Investigator Brochures, INDs and marketing applications.
Collaborate with the Clinical Development Lead in the oversight of clinical studies. May lead a clinical study with oversight from the Clinical Development Lead to provide clinical study leadership, review and interpretation of clinical data, and ensure timely execution of deliverables in collaboration with internal and external partners. Perform and coordinate clinical data review and analysis of study data, including review of case report forms, data listings, medical coding and patient profiles to ensure the proper and complete verification of clinical data.
In collaboration with the Clinical Development Lead and Clinical Safety & Pharmacovigilance, support managing study sites to ensure that study treatment discontinuation or other safety decisions are made in alignment with the protocol.
Collaborating with Clinical Operations, participate in the start-up and execution of global clinical studies to ensure on-schedule site activation and subject enrollment of a clinical trial. Design and implement clinical study parameters to minimize operational risk and increase study site performance and efficiency. Collaborate on and contribute to inspection readiness activities that support audits and regulatory inspections related to clinical trial conduct
Develop the strategy and drive the messaging and associated content for Investigator Meetings, investigator engagement and Advisory Board meetings.
Responsibility for training and educating junior Clinical Science personnel.
Support and help drive the evolution of the clinical science role at Moderna and support process updates. Participate in Development workstreams related to the clinical trial delivery operating model.
A personal and professional commitment to the highest personal and ethical standards.
A high-performing, self-motivated and energetic individual who demonstrates outstanding scientific and clinical oncology knowledge that results in the conduct of well-executed clinical research.
A history of successfully operating in a matrix environment and the demonstration of highly developed interpersonal and communication skills.
Capability to successfully contribute to both early and late-stage clinical development programs. This will involve close with Drug Discovery, Translational Medicine, Regulatory Affairs, Biostatistics, Medical Affairs and Commercial.
The individual must have the demonstrated ability to successfully work in a team environment.
This role is best suited for candidates holding a PhD, PharmD, Masters’ or advanced nursing degree with significant scientific and clinical oncology knowledge, pharmaceutical/biotechnology company experience and a comprehensive knowledge of drug development.
A minimum of 10 years of clinical development experience within a pharmaceutical/biotechnology company.
Significant experience with clinical study design and protocol development.
Significant experience with ensuring data integrity, data analysis and data presentation.
Excellent written communication, oral communication, and presentation skills.
Ability to travel up to 15% required for travel to work with study sites and attend national and international scientific congresses.
This role is based in our new LEED-certified HQ in Cambridge, MA, or Princeton, NJ office and is expected to be in-office 70% of the time with flexibility to work from home up to 30%.
At Moderna, we believe that when you feel your best, you can do your best work. That’s why our benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.
Moderna is a smoke-free, alcohol-free, and drug-free work environment.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.
We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at [email protected].
Export Control Notice This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant’s ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license. #LI-NH1-
Our mission is to deliver the greatest possible impact to people through mRNA medicines.
Moderna is a pioneer and leader in the field of mRNA medicine. Through the advancement of its technology platform, Moderna is reimagining how medicines are made to transform how we treat and prevent diseases. Since its founding, Moderna's mRNA platform has enabled the development of vaccines and therapeutics across infectious diseases, cancer, rare diseases and more. With a global team and a unique culture, driven by the company's values and mindsets, Moderna's mission is to deliver the greatest possible impact to people through mRNA medicines. For more information about Moderna, please visit modernatx.com and connect with us on X, Facebook, Instagram, YouTube and LinkedIn. This Moderna page is not the appropriate place to report adverse events (side-effects) for any products. If you are or someone you know is experiencing a side effect, please reach out to your healthcare professional. Moderna is continuously monitoring the safety of its products. We encourage you to report any side effects directly to us at 1‑866‑MODERNA (1‑866‑663‑3762). Please be cautious of fraudulent recruitment offers claiming to be from Moderna. Recruitment scams of this sort may originate from fake websites, social media accounts, or unsolicited communications and may ask you for personal information or request you pay them or someone else. Moderna will never ask you for payment, banking information, or anything of this sort at any stage of the recruitment process. If you are unsure about a communication, do not provide personal information and report the activity to [email protected]. You may also report suspected fraud to the FBI’s Internet Crime Complaint Center (IC3).
Offices: 200 Technology Sq, Cambridge, Massachusetts 02139, US · 1 Upland Rd, Norwood, Massachusetts 02062, US
Based on 1875 listings with disclosed salaries, most science & research jobs in New Jersey pay between $87k–$233k per year. Individual offers vary with seniority, company size, and specialization.
There are currently 3,452 open science & research positions in New Jersey listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include MSD, Hackensack Meridian Health, Bristol Myers Squibb, Atlantic Health, Laboratory Corporation of America Holdings, among others. Browse the listings above to see every active employer.
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